Year |
Citation |
Score |
2020 |
Reddy Vakiti J, Hanessian S. Total Synthesis and Stereochemical Confirmation of (-)-Olivil, (+)-Cycloolivil, (-)-Alashinols F and G, (+)-Cephafortin A, and Their Congeners: Filling in Biosynthetic Gaps. Organic Letters. 22: 3345-3350. PMID 32293189 DOI: 10.1021/Acs.Orglett.0C00773 |
0.32 |
|
2020 |
Hocine S, Berger G, Hanessian S. Design and Synthesis of Backbone-Fused, Conformationally Constrained Morpholine-Proline Chimeras. The Journal of Organic Chemistry. PMID 32134267 DOI: 10.1021/Acs.Joc.9B03413.S001 |
0.35 |
|
2020 |
Bodwell G, Hanessian S. Professor James D. Wuest Canadian Journal of Chemistry. 98. DOI: 10.1139/Cjc-2020-0179 |
0.532 |
|
2019 |
Garsi JB, Vece V, Sernissi L, Auger-Morin C, Hanessian S, McCracken AN, Selwan E, Ramirez C, Dahal A, Romdhane NB, Finicle BT, Edinger AL. Design, synthesis and anticancer activity of constrained sphingolipid-phenoxazine/phenothiazine hybrid constructs targeting protein phosphatase 2A. Bioorganic & Medicinal Chemistry Letters. PMID 31383588 DOI: 10.1016/J.Bmcl.2019.07.023 |
0.327 |
|
2019 |
Salinas JC, Seth PP, Hanessian S. Design And Synthesis Of An Azabicyclic Nucleoside Phosphoramidite For Oligonucleotide Antisense Constructs. Nucleosides, Nucleotides & Nucleic Acids. 1-23. PMID 31380707 DOI: 10.1080/15257770.2019.1646916 |
0.352 |
|
2019 |
Duchamp E, Simard BD, Hanessian S. Reductive Fragmentation of Tetrazoles: Mechanistic Insights and Applications toward the Stereocontrolled Synthesis of 2,6-Polysubstituted Morpholines. Organic Letters. PMID 31240939 DOI: 10.1021/Acs.Orglett.9B01842 |
0.39 |
|
2018 |
Rico L, Hanessian S. Synthesis of 1',2'-methano-2',3'-dideoxynucleosides as potential antivirals. Bioorganic & Medicinal Chemistry Letters. PMID 30612845 DOI: 10.1016/J.Bmcl.2018.12.054 |
0.369 |
|
2018 |
Garsi JB, Sernissi L, Vece V, Hanessian S, McCracken AN, Simitian G, Edinger AL. In search of constrained FTY720 and phytosphingosine analogs as dual acting anticancer agents targeting metabolic and epigenetic pathways. European Journal of Medicinal Chemistry. 159: 217-242. PMID 30292898 DOI: 10.1016/J.Ejmech.2018.09.043 |
0.301 |
|
2018 |
Salinas JC, Yu J, Østergaard M, Seth PP, Hanessian S. Conception and Synthesis of Oxabicyclic Nucleoside Phosphonates as Internucleotidic Phosphate Surrogates in Antisense Oligonucleotide Constructs. Organic Letters. PMID 30146887 DOI: 10.1021/Acs.Orglett.8B02233 |
0.369 |
|
2018 |
Vece V, Jakkepally S, Hanessian S. Total Synthesis and Absolute Stereochemical Assignment of the Insecticidal Metabolites Yaequinolones J1 and J2. Organic Letters. 20: 4277-4280. PMID 29975546 DOI: 10.1021/Acs.Orglett.8B01701 |
0.375 |
|
2018 |
Kanazawa H, Saavedra OM, Maianti JP, Young SA, Izquierdo L, Smith TK, Hanessian S, Kondo J. Structure-Based Design of a Eukaryote-Selective Antiprotozoal Fluorinated Aminoglycoside. Chemmedchem. PMID 29766661 DOI: 10.1002/Cmdc.201800166 |
0.787 |
|
2017 |
Chattopadhyay AK, Hanessian S. Recent Progress in the Chemistry of Daphniphyllum Alkaloids †. Chemical Reviews. PMID 28205435 DOI: 10.1021/Acs.Chemrev.6B00412 |
0.319 |
|
2017 |
Chénard É, Cusson J, Hanessian S. Catalytic asymmetric Friedel–Crafts synthesis of 1,1′-diaryl-2-substituted 4-pentenes enables stereoselective access to functionalized tetrahydronaphthalenes Canadian Journal of Chemistry. 95: 1323-1331. DOI: 10.1139/Cjc-2017-0393 |
0.404 |
|
2016 |
St-Pierre G, Hanessian S. Solution and Solid-Phase Stereocontrolled Synthesis of 1,2-cis-Glycopyranosides with Minimally Protected Glycopyranosyl Donors Catalyzed by BF3-N,N-Dimethylformamide Complex. Organic Letters. PMID 27301355 DOI: 10.1021/Acs.Orglett.6B01263 |
0.358 |
|
2016 |
Chattopadhyay AK, Berger G, Hanessian S. Strategies toward the Total Synthesis of Calyciphylline B-type Alkaloids: A Computational Perspective Aided by DFT Analysis. The Journal of Organic Chemistry. PMID 27251014 DOI: 10.1021/Acs.Joc.6B00638 |
0.338 |
|
2016 |
Chattopadhyay AK, Menz H, Ly VL, Dorich S, Hanessian S. Synthesis of a Model Tetracyclic Core Structure of Calyciphylline B-Type Alkaloids. The Journal of Organic Chemistry. PMID 26878089 DOI: 10.1021/Acs.Joc.5B02875 |
0.776 |
|
2016 |
Büschleb M, Dorich S, Hanessian S, Tao D, Schenthal KB, Overman LE. Synthetic Strategies toward Natural Products Containing Contiguous Stereogenic Quaternary Carbon Atoms. Angewandte Chemie (International Ed. in English). PMID 26836448 DOI: 10.1002/Anie.201507549 |
0.784 |
|
2016 |
Chattopadhyay AK, Ly VL, Jakkepally S, Berger G, Hanessian S. Total Synthesis of Isodaphlongamine H: A Possible Biogenetic Conundrum. Angewandte Chemie (International Ed. in English). PMID 26765928 DOI: 10.1002/Anie.201510861 |
0.793 |
|
2016 |
Giacometti RD, Salinas JC, Østergaard ME, Swayze EE, Seth PP, Hanessian S. Design, synthesis, and duplex-stabilizing properties of conformationally constrained tricyclic analogues of LNA. Organic & Biomolecular Chemistry. PMID 26765794 DOI: 10.1039/C5Ob02576A |
0.378 |
|
2016 |
Hanessian S, St-Pierre G, Dafik L, Klegraf E. Stereocontrolled Synthesis of Phenolic α-d-Glycopyranosides Synthesis. 48: 3575-3588. DOI: 10.1055/S-0035-1561461 |
0.348 |
|
2016 |
Maianti JP, Hanessian S. Structural hybridization of three aminoglycoside antibiotics yields a potent broad-spectrum bactericide that eludes bacterial resistance enzymes Medchemcomm. 7: 170-176. DOI: 10.1039/C5Md00429B |
0.787 |
|
2016 |
Büschleb M, Dorich S, Hanessian S, Tao D, Schenthal KB, Overman LE. Strategien für die Synthese von Naturstoffen mit benachbarten stereogenen quartären Kohlenstoffatomen Angewandte Chemie. 128: 4226-4258. DOI: 10.1002/Ange.201507549 |
0.769 |
|
2015 |
Chattopadhyay AK, Hanessian S. Cyclic enaminones. Part II: applications as versatile intermediates in alkaloid synthesis. Chemical Communications (Cambridge, England). 51: 16450-67. PMID 26490499 DOI: 10.1039/C5Cc05892A |
0.38 |
|
2015 |
Chattopadhyay AK, Hanessian S. Cyclic enaminones. Part I: stereocontrolled synthesis using diastereoselective and catalytic asymmetric methods. Chemical Communications (Cambridge, England). 51: 16437-49. PMID 26490402 DOI: 10.1039/C5Cc05891K |
0.421 |
|
2015 |
Berger G, Vilchis-Reyes M, Hanessian S. Structural Properties and Stereochemically Distinct Folding Preferences of 4,5-cis and trans-Methano-L-Proline Oligomers: The Shortest Crystalline PPII-Type Helical Proline-Derived Tetramer. Angewandte Chemie (International Ed. in English). 54: 13268-72. PMID 26346999 DOI: 10.1002/Anie.201506208 |
0.304 |
|
2015 |
Cusson JP, Chénard E, Hanessian S. On the importance of the relative stereochemistry of substituents in the formation of nine-membered lactones by ring-closing metathesis Synthesis (Germany). 47: 1317-1324. DOI: 10.1055/S-0034-1380130 |
0.373 |
|
2015 |
Grelier G, Chénard E, Büschleb M, Hanessian S. Proximity- and chelation-induced SNAr 1,4-aromatic ortho-substitution of ortho-methoxyphenyl 2-alkyl ketones Synthesis (Germany). 47: 1091-1100. DOI: 10.1055/S-0034-1379992 |
0.361 |
|
2014 |
Salinas JC, Migawa MT, Merner BL, Hanessian S. Alternative syntheses of (S)-cEt-BNA: a key constrained nucleoside component of bioactive antisense gapmer sequences. The Journal of Organic Chemistry. 79: 11651-60. PMID 25401196 DOI: 10.1021/Jo502320Y |
0.786 |
|
2014 |
Hanessian S, Chénard E, Guesné S, Cusson JP. Conception and evolution of stereocontrolled strategies toward functionalized 8-aryloctanoic acids related to the total synthesis of aliskiren. The Journal of Organic Chemistry. 79: 9531-45. PMID 25285791 DOI: 10.1021/Jo5015195 |
0.407 |
|
2014 |
Focken T, Hanessian S. Application of cyclic phosphonamide reagents in the total synthesis of natural products and biologically active molecules. Beilstein Journal of Organic Chemistry. 10: 1848-77. PMID 25246946 DOI: 10.3762/Bjoc.10.195 |
0.413 |
|
2014 |
Maianti JP, Kanazawa H, Dozzo P, Matias RD, Feeney LA, Armstrong ES, Hildebrandt DJ, Kane TR, Gliedt MJ, Goldblum AA, Linsell MS, Aggen JB, Kondo J, Hanessian S. Toxicity modulation, resistance enzyme evasion, and A-site X-ray structure of broad-spectrum antibacterial neomycin analogs. Acs Chemical Biology. 9: 2067-73. PMID 25019242 DOI: 10.1021/Cb5003416 |
0.791 |
|
2014 |
Chénard E, Hanessian S. Kinetic diastereomer differentiation in Au(III)- and Bi(III)-catalyzed benzylic arylation: concise and stereocontrolled synthesis of 2-amino-1,1-diarylalkanes. Organic Letters. 16: 2668-71. PMID 24805004 DOI: 10.1021/Ol500902P |
0.349 |
|
2014 |
Hanessian S, Chattopadhyay AK. Iminium ion-enamine cascade cyclizations: facile access to structurally diverse azacyclic compounds and natural products. Organic Letters. 16: 232-5. PMID 24341416 DOI: 10.1021/Ol403229Q |
0.335 |
|
2014 |
Hanessian S, Mu C. Yb(OTf)3-Mediated Ring Opening of Functionalized Cyclopentane Epoxides with Aniline: Aspects of Regiochemistry and Stereochemistry Heterocycles. 88: 1553. DOI: 10.3987/Com-13-S(S)85 |
0.324 |
|
2014 |
Dorich S, Del Valle JR, Hanessian S. Synthesis of functionalized octahydroindoles related to daphnyphyllum alkaloids Synlett. 25: 799-804. DOI: 10.1055/S-0033-1340794 |
0.782 |
|
2014 |
Hanessian S, Saavedra OM, Vilchis-Reyes MA, Maianti JP, Kanazawa H, Dozzo P, Matias RD, Serio A, Kondo J. Synthesis, broad spectrum antibacterial activity, and X-ray co-crystal structure of the decoding bacterial ribosomal A-site with 4′-deoxy-4′-fluoro neomycin analogs Chemical Science. 5: 4621-4632. DOI: 10.1039/C4Sc01626B |
0.803 |
|
2014 |
Hanessian S, Saavedra OM, Vilchis-Reyes MA, Llaguno-Rueda AM. Synthesis of 4′-deoxy-4′-fluoro neamine and 4′-deoxy-4′-fluoro 4′-epi neamine Medchemcomm. 5: 1166-1171. DOI: 10.1039/C4Md00072B |
0.381 |
|
2014 |
Hanessian S, Dorich S, Kassem S, Menz H, Chattopadhyay AK. Stereocontrolled synthesis of all-syn 3,4-disubstituted l-prolines: Studies of the reductive rearrangement of unactivated tertiary allylic alcohols Tetrahedron. 70: 439-449. DOI: 10.1016/J.Tet.2013.11.040 |
0.777 |
|
2014 |
Sánchez-Larios E, Giacometti RD, Hanessian S. Application and scope of Schreiber's gold(I)-catalyzed α-pyrone synthesis to ring a aromatic podolactones European Journal of Organic Chemistry. 2014: 5664-5669. DOI: 10.1002/Ejoc.201402803 |
0.385 |
|
2014 |
Del Valle JR, Therrien E, Hanessian S. Aeruginosins as Thrombin Inhibitors Natural Products in Medicinal Chemistry. 333-364. DOI: 10.1002/9783527676545.ch10 |
0.585 |
|
2013 |
Hanessian S, Schroeder BR, Merner BL, Chen B, Swayze EE, Seth PP. Synthesis of cis- and trans-α-l-[4.3.0]bicyclo-DNA monomers for antisense technology: methods for the diastereoselective formation of bicyclic nucleosides. The Journal of Organic Chemistry. 78: 9051-63. PMID 23937280 DOI: 10.1021/Jo401166Q |
0.79 |
|
2013 |
Hanessian S, Wagger J, Merner BL, Giacometti RD, Ostergaard ME, Swayze EE, Seth PP. A constrained tricyclic nucleic acid analogue of α-L-LNA: investigating the effects of dual conformational restriction on duplex thermal stability. The Journal of Organic Chemistry. 78: 9064-75. PMID 23937256 DOI: 10.1021/Jo401170Y |
0.754 |
|
2013 |
Hanessian S, Dorich S, Chattopadhyay AK, Büschleb M. Studies toward the generation of functionalized quaternary carbon centers relying on Wittig and Wittig-Still allylic ether anionic transpositions. The Journal of Organic Chemistry. 78: 8915-21. PMID 23915281 DOI: 10.1021/Jo401488Y |
0.786 |
|
2013 |
Hanessian S, Dorich S, Menz H. Concise and stereocontrolled synthesis of the tetracyclic core of daphniglaucin C. Organic Letters. 15: 4134-7. PMID 23889206 DOI: 10.1021/Ol4018112 |
0.799 |
|
2013 |
Tourigny DS, Fernández IS, Kelley AC, Vakiti RR, Chattopadhyay AK, Dorich S, Hanessian S, Ramakrishnan V. Crystal structure of a bioactive pactamycin analog bound to the 30S ribosomal subunit. Journal of Molecular Biology. 425: 3907-10. PMID 23702293 DOI: 10.1016/J.Jmb.2013.05.004 |
0.787 |
|
2013 |
Kondo J, Koganei M, Maianti JP, Ly VL, Hanessian S. Crystal structures of a bioactive 6'-hydroxy variant of sisomicin bound to the bacterial and protozoal ribosomal decoding sites. Chemmedchem. 8: 733-9. PMID 23436717 DOI: 10.1002/Cmdc.201200579 |
0.773 |
|
2013 |
Hanessian S, Vakiti RR, Chattopadhyay AK, Dorich S, Lavallée C. Probing functional diversity in pactamycin toward antibiotic, antitumor, and antiprotozoal activity. Bioorganic & Medicinal Chemistry. 21: 1775-86. PMID 23434136 DOI: 10.1016/J.Bmc.2013.01.037 |
0.779 |
|
2013 |
Kondo J, Koganei M, Maianti JP, Ly VL, Hanessian S. Back Cover: Crystal Structures of a Bioactive 6′-Hydroxy Variant of Sisomicin Bound to the Bacterial and Protozoal Ribosomal Decoding Sites (ChemMedChem 5/2013) Chemmedchem. 8: 864-864. DOI: 10.1002/Cmdc.201390019 |
0.761 |
|
2012 |
Hanessian S, Vakiti RR, Dorich S, Banerjee S, Deschênes-Simard B. Total synthesis of pactamycin and pactamycate: a detailed account. The Journal of Organic Chemistry. 77: 9458-72. PMID 23083207 DOI: 10.1021/Jo301638Z |
0.816 |
|
2012 |
Hanessian S, Schroeder BR, Giacometti RD, Merner BL, Ostergaard M, Swayze EE, Seth PP. Structure-based design of a highly constrained nucleic acid analogue: improved duplex stabilization by restricting sugar pucker and torsion angle γ. Angewandte Chemie (International Ed. in English). 51: 11242-5. PMID 22915274 DOI: 10.1002/Anie.201203680 |
0.772 |
|
2012 |
Hanessian S. The enterprise of synthesis: from concept to practice. The Journal of Organic Chemistry. 77: 6657-88. PMID 22784216 DOI: 10.1021/Jo300902M |
0.337 |
|
2012 |
Hanessian S, Chénard E. A new approach to the synthesis of peptidomimetic renin inhibitors: palladium-catalyzed asymmetric allylation of acyclic alkyl aryl ketones. Organic Letters. 14: 3222-5. PMID 22668074 DOI: 10.1021/Ol301332F |
0.411 |
|
2012 |
Hanessian S, Maianti JP, Ly VL, Deschênes-Simard B. Structural and kinetic study of self-assembling macrocyclic dimer natural product aminoglycoside 66-40C and unnatural variants Chemical Science. 3: 249-256. DOI: 10.1039/C1Sc00538C |
0.766 |
|
2011 |
Hanessian S, Giguère A, Grzyb J, Maianti JP, Saavedra OM, Aggen JB, Linsell MS, Goldblum AA, Hildebrandt DJ, Kane TR, Dozzo P, Gliedt MJ, Matias RD, Feeney LA, Armstrong ES. Toward Overcoming Staphylococcus aureus Aminoglycoside Resistance Mechanisms with a Functionally Designed Neomycin Analogue. Acs Medicinal Chemistry Letters. 2: 924-8. PMID 24900282 DOI: 10.1021/Ml200202Y |
0.788 |
|
2011 |
Hanessian S, Maianti JP, Matias RD, Feeney LA, Armstrong ES. Hybrid aminoglycoside antibiotics via Tsuji palladium-catalyzed allylic deoxygenation. Organic Letters. 13: 6476-9. PMID 22085292 DOI: 10.1021/Ol2027703 |
0.795 |
|
2011 |
Hanessian S, Vakiti RR, Dorich S, Banerjee S, Lecomte F, DelValle JR, Zhang J, Deschênes-Simard B. Total synthesis of pactamycin. Angewandte Chemie (International Ed. in English). 50: 3497-500. PMID 21370372 DOI: 10.1002/Anie.201008079 |
0.809 |
|
2011 |
Hanessian S, Soma U, Dorich S, Deschênes-Simard B. Total synthesis of (+)-ent-cyclizidine: absolute configurational confirmation of antibiotic M146791. Organic Letters. 13: 1048-51. PMID 21271743 DOI: 10.1021/Ol103094J |
0.82 |
|
2011 |
Hanessian S, Stoffman E, Mi X, Renton P. Applications of organocatalytic asymmetric synthesis to drug prototypes--dual action and selective inhibitors of n-nitric oxide synthase with activity against the 5-HT1D/1B subreceptors. Organic Letters. 13: 840-3. PMID 21271688 DOI: 10.1021/Ol102795G |
0.359 |
|
2011 |
Hanessian S, Focken T, Oza R. Lewis-acid catalyzed formation of dihydropyrans Tetrahedron. 67: 9870-9884. DOI: 10.1016/J.Tet.2011.09.069 |
0.403 |
|
2011 |
Hanessian S, Vakiti RR, Dorich S, Banerjee S, Lecomte F, DelValle JR, Zhang J, Deschênes-Simard B. Cover Picture: Total Synthesis of Pactamycin (Angew. Chem. Int. Ed. 15/2011) Angewandte Chemie International Edition. 50: 3325-3325. DOI: 10.1002/Anie.201101592 |
0.797 |
|
2011 |
Hanessian S, Vakiti RR, Dorich S, Banerjee S, Lecomte F, DelValle JR, Zhang J, Deschênes-Simard B. Titelbild: Total Synthesis of Pactamycin (Angew. Chem. 15/2011) Angewandte Chemie. 123: 3383-3383. DOI: 10.1002/Ange.201101592 |
0.81 |
|
2010 |
Hanessian S, Auzzas L, Larsson A, Zhang J, Giannini G, Gallo G, Ciacci A, Cabri W. Vorinostat-like molecules as structural, stereochemical, and pharmacological tools. Acs Medicinal Chemistry Letters. 1: 70-4. PMID 24900179 DOI: 10.1021/Ml100028G |
0.581 |
|
2010 |
Auzzas L, Larsson A, Matera R, Baraldi A, Deschênes-Simard B, Giannini G, Cabri W, Battistuzzi G, Gallo G, Ciacci A, Vesci L, Pisano C, Hanessian S. Non-natural macrocyclic inhibitors of histone deacetylases: design, synthesis, and activity. Journal of Medicinal Chemistry. 53: 8387-99. PMID 21073160 DOI: 10.1021/Jm101092U |
0.596 |
|
2010 |
Hanessian S, Larsson A, Fex T, Knecht W, Blomberg N. Design and synthesis of macrocyclic indoles targeting blood coagulation cascade Factor XIa. Bioorganic & Medicinal Chemistry Letters. 20: 6925-8. PMID 21035339 DOI: 10.1016/J.Bmcl.2010.09.141 |
0.333 |
|
2010 |
Hanessian S, Pachamuthu K, Szychowski J, Giguère A, Swayze EE, Migawa MT, François B, Kondo J, Westhof E. Structure-based design, synthesis and A-site rRNA co-crystal complexes of novel amphiphilic aminoglycoside antibiotics with new binding modes: a synergistic hydrophobic effect against resistant bacteria. Bioorganic & Medicinal Chemistry Letters. 20: 7097-101. PMID 20970332 DOI: 10.1016/J.Bmcl.2010.09.084 |
0.342 |
|
2010 |
Hanessian S, Focken T, Mi X, Oza R, Chen B, Ritson D, Beaudegnies R. Total synthesis of (+)-ambruticin S: probing the pharmacophoric subunit. The Journal of Organic Chemistry. 75: 5601-18. PMID 20704433 DOI: 10.1021/Jo100956V |
0.427 |
|
2010 |
Hanessian S, Focken T, Oza R. Total synthesis of jerangolid A. Organic Letters. 12: 3172-5. PMID 20565089 DOI: 10.1021/Ol101103Q |
0.432 |
|
2010 |
Hanessian S, Maji DK, Govindan S, Matera R, Tintelnot-Blomley M. Substrate-controlled and organocatalytic asymmetric synthesis of carbocyclic amino acid dipeptide mimetics. The Journal of Organic Chemistry. 75: 2861-76. PMID 20392053 DOI: 10.1021/Jo100017T |
0.355 |
|
2010 |
Hanessian S, Guesné S, Chénard E. Total synthesis of "aliskiren": the first Renin inhibitor in clinical practice for hypertension. Organic Letters. 12: 1816-9. PMID 20235519 DOI: 10.1021/Ol100427V |
0.371 |
|
2010 |
Hanessian S, Maianti JP. Biomimetic synthesis and structural refinement of the macrocyclic dimer aminoglycoside 66-40C--the remarkably selective self-condensation of a putative aldehyde intermediate in the submerged culture medium producing sisomicin. Chemical Communications (Cambridge, England). 46: 2013-5. PMID 20221476 DOI: 10.1039/B925668G |
0.803 |
|
2010 |
Hanessian S, Deschênes-Simard B, Simard D, Chenel C, Haak E, Bulat V. Proximity-assisted cycloaddition reactions of ω-azido cyanohydrin ethers: Synthesis of diversely functionalized bicyclic tetrazoles Pure and Applied Chemistry. 82: 1761-1771. DOI: 10.1351/Pac-Con-09-08-08 |
0.358 |
|
2010 |
Hanessian S, Mi X. An organocatalytic approach to enantiopure 2,6-disubstituted tetrahydropyranols Synlett. 761-764. DOI: 10.1055/S-0029-1219354 |
0.378 |
|
2009 |
Hanessian S, Boyer N, Reddy GJ, Deschênes-Simard B. Total synthesis of oidiodendrolides and related norditerpene dilactones from a common precursor: metabolites CJ-14,445, LL-Z1271gamma, oidiolactones A, B, C, and D, and nagilactone F. Organic Letters. 11: 4640-3. PMID 19778011 DOI: 10.1021/Ol901896C |
0.392 |
|
2009 |
Hanessian S, Wang X, Ersmark K, Del Valle JR, Klegraf E. Total synthesis and structural revision of the presumed aeruginosins 205A and B. Organic Letters. 11: 4232-5. PMID 19691354 DOI: 10.1021/Ol901702K |
0.668 |
|
2009 |
Hanessian S, Therrien E, Zhang J, Otterlo Wv, Xue Y, Gustafsson D, Nilsson I, Fjellström O. From natural products to achiral drug prototypes: potent thrombin inhibitors based on P2/P3 dihydropyrid-2-one core motifs. Bioorganic & Medicinal Chemistry Letters. 19: 5429-32. PMID 19674897 DOI: 10.1016/J.Bmcl.2009.07.107 |
0.302 |
|
2009 |
Hanessian S, Szychowski J, Maianti JP. Synthesis and comparative antibacterial activity of verdamicin C2 and C2a. A new oxidation of primary allylic azides in dihydro[2H]pyrans. Organic Letters. 11: 429-32. PMID 19072132 DOI: 10.1021/Ol802421D |
0.78 |
|
2009 |
Hanessian S. Structure-based synthesis: From natural products to drug prototypes Pure and Applied Chemistry. 81: 1085-1091. DOI: 10.1351/Pac-Con-08-07-12 |
0.42 |
|
2009 |
Hanessian S, Riber L, Marin J. Diastereoselective synthesis of functionally diverse substituted pipecolic acids Synlett. 71-74. DOI: 10.1055/S-0028-1087477 |
0.397 |
|
2009 |
Del Valle JR, Wang X, Ersmark K, Hanessian S. β-substituted D-leucines and their relevance in the total synthesis of natural and unnatural aeruginosins Acs Symposium Series. 1009: 443-461. DOI: 10.1021/bk-2009-1009.ch027 |
0.653 |
|
2009 |
Hanessian S, Deschênes-Simard B, Simard D. Exploring the unique reactivities of heterobicyclic tetrazoles-access to functionally diverse and versatile heterocyclic scaffolds Tetrahedron. 65: 6656-6669. DOI: 10.1016/J.Tet.2009.06.033 |
0.37 |
|
2008 |
Hanessian S, Auzzas L. The practice of ring constraint in peptidomimetics using bicyclic and polycyclic amino acids. Accounts of Chemical Research. 41: 1241-51. PMID 18646869 DOI: 10.1021/Ar8000052 |
0.389 |
|
2008 |
Hanessian S, Simard D, Deschênes-Simard B, Chenel C, Haak E. Proximity-assisted cycloaddition reactions--facile Lewis acid-mediated synthesis of diversely functionalized bicyclic tetrazoles. Organic Letters. 10: 1381-4. PMID 18314995 DOI: 10.1021/Ol703071C |
0.386 |
|
2008 |
Hanessian S, Simard D, Bayrakdarian M, Therrien E, Nilsson I, Fjellström O. Design, synthesis, and thrombin-inhibitory activity of pyridin-2-ones as P2/P3 core motifs. Bioorganic & Medicinal Chemistry Letters. 18: 1972-6. PMID 18289852 DOI: 10.1016/J.Bmcl.2008.01.122 |
0.774 |
|
2008 |
Hanessian S, Auzzas L. Alternative and expedient asymmetric syntheses of L-(+)-noviose. Organic Letters. 10: 261-4. PMID 18081305 DOI: 10.1021/Ol702655C |
0.332 |
|
2008 |
Ersmark K, Del Valle JR, Hanessian S. Chemistry and biology of the aeruginosin family of serine protease inhibitors. Angewandte Chemie (International Ed. in English). 47: 1202-23. PMID 18076006 DOI: 10.1002/Anie.200605219 |
0.667 |
|
2008 |
Hanessian S, Vinci V, Fettis K, Maris T, Viet MT. Self-assembly of noncyclic bis-D- and L-tripeptides into higher order tubular constructs: design, synthesis, and X-ray crystal superstructure. The Journal of Organic Chemistry. 73: 1181-91. PMID 18062697 DOI: 10.1021/Jo701621C |
0.34 |
|
2008 |
Hanessian S, Hocquelet C, Jankowski CK. Synthesis of aminocyclodextrin carboxylic acids Synlett. 715-719. DOI: 10.1055/S-2008-1042803 |
0.364 |
|
2007 |
Hanessian S, Auzzas L, Giannini G, Marzi M, Cabri W, Barbarino M, Vesci L, Pisano C. Omega-alkoxy analogues of SAHA (vorinostat) as inhibitors of HDAC: a study of chain-length and stereochemical dependence. Bioorganic & Medicinal Chemistry Letters. 17: 6261-5. PMID 17892933 DOI: 10.1016/J.Bmcl.2007.09.014 |
0.598 |
|
2007 |
Kondo J, Pachamuthu K, François B, Szychowski J, Hanessian S, Westhof E. Crystal structure of the bacterial ribosomal decoding site complexed with a synthetic doubly functionalized paromomycin derivative: a new specific binding mode to an a-minor motif enhances in vitro antibacterial activity. Chemmedchem. 2: 1631-8. PMID 17722211 DOI: 10.1002/Cmdc.200700113 |
0.352 |
|
2007 |
Loiseleur O, Ritson D, Nina M, Crowley P, Wagner T, Hanessian S. Ring-modified analogues and molecular dynamics studies to probe the requirements for fungicidal activities of malayamycin A and its N-nucleoside variants. The Journal of Organic Chemistry. 72: 6353-63. PMID 17658846 DOI: 10.1021/Jo070520D |
0.339 |
|
2007 |
Hanessian S, Szychowski J, Adhikari SS, Vasquez G, Kandasamy P, Swayze EE, Migawa MT, Ranken R, François B, Wirmer-Bartoschek J, Kondo J, Westhof E. Structure-based design, synthesis, and A-site rRNA cocrystal complexes of functionally novel aminoglycoside antibiotics: C2" ether analogues of paromomycin. Journal of Medicinal Chemistry. 50: 2352-69. PMID 17458946 DOI: 10.1021/Jm061200+ |
0.383 |
|
2007 |
Hanessian S, Ersmark K, Wang X, Del Valle JR, Blomberg N, Xue Y, Fjellström O. Structure-based organic synthesis of unnatural aeruginosin hybrids as potent inhibitors of thrombin. Bioorganic & Medicinal Chemistry Letters. 17: 3480-5. PMID 17428662 DOI: 10.1016/J.Bmcl.2007.03.075 |
0.668 |
|
2007 |
Hanessian S, Szychowski J, Campos-Reales Pineda NB, Furtos A, Keillor JW. 6-hydroxy to 6'''-amino tethered ring-to-ring macrocyclic aminoglycosides as probes for APH(3')-IIIa kinase. Bioorganic & Medicinal Chemistry Letters. 17: 3221-5. PMID 17400454 DOI: 10.1016/J.Bmcl.2007.03.014 |
0.338 |
|
2007 |
Hanessian S, Reddy GJ. Total synthesis and stereochemical confirmation of 2,5-diaryl-3,4- dimethyltetrahydrofuran lignans: (+)-Fragransin A2, (+)-galbelgin, (+)-talaumidin, (-)-saucernetin and (-)-verrucosin Synlett. 475-479. DOI: 10.1055/S-2007-968019 |
0.418 |
|
2007 |
Hanessian S, Adhikari S, Szychowski J, Pachamuthu K, Wang X, Migawa MT, Griffey RH, Swayze EE. Corrigendum to "Probing the ribosomal RNA A-site with functionally diverse analogues of paromomycin-synthesis of ring I mimetics". [Tetrahedron 63 (2007) 827-846] (DOI:10.1016/j.tet.2006.10.079) Tetrahedron. 63: 5329. DOI: 10.1016/J.Tet.2007.03.161 |
0.351 |
|
2007 |
Hanessian S, Adhikari S, Szychowski J, Pachamuthu K, Wang X, Migawa MT, Griffey RH, Swayze EE. Probing the ribosomal RNA A-site with functionally diverse analogues of paromomycin-synthesis of ring I mimetics Tetrahedron. 63: 827-846. DOI: 10.1016/J.Tet.2006.10.079 |
0.416 |
|
2006 |
Hanessian S, Ritson DJ. Structure-based organic synthesis of a tricyclic N-malayamycin analogue. The Journal of Organic Chemistry. 71: 9807-17. PMID 17168600 DOI: 10.1021/Jo061904R |
0.374 |
|
2006 |
Hanessian S, Giroux S, Larsson A. Efficient allyl to propenyl isomerization in functionally diverse compounds with a thermally modified Grubbs second-generation catalyst. Organic Letters. 8: 5481-4. PMID 17107052 DOI: 10.1021/Ol062167O |
0.754 |
|
2006 |
Hanessian S, Reddy GJ, Chahal N. Total synthesis and stereochemical confirmation of manassantin A, B, and B1. Organic Letters. 8: 5477-80. PMID 17107051 DOI: 10.1021/Ol0621710 |
0.304 |
|
2006 |
Hanessian S, Shao Z, Warrier JS. Optimization of the catalytic asymmetric addition of nitroalkanes to cyclic enones with trans-4,5-methano-L-proline. Organic Letters. 8: 4787-90. PMID 17020303 DOI: 10.1021/Ol0618407 |
0.352 |
|
2006 |
Hanessian S, Chahal N, Giroux S. Iterative synthesis of deoxypropionate units: the inductor effect in acyclic conformation design. The Journal of Organic Chemistry. 71: 7403-11. PMID 16958535 DOI: 10.1021/Jo061098O |
0.761 |
|
2006 |
Hanessian S, Mainetti E, Lecomte F. Synthesis and stereochemical confirmation of the secoiridoid glucosides nudiflosides D and A. Organic Letters. 8: 4047-9. PMID 16928070 DOI: 10.1021/Ol0615230 |
0.359 |
|
2006 |
Hanessian S, Del Valle JR, Xue Y, Blomberg N. Total synthesis and structural confirmation of chlorodysinosin A. Journal of the American Chemical Society. 128: 10491-5. PMID 16895415 DOI: 10.1021/Ja0625834 |
0.708 |
|
2006 |
Hanessian S, Vinci V, Auzzas L, Marzi M, Giannini G. Exploring alternative Zn-binding groups in the design of HDAC inhibitors: squaric acid, N-hydroxyurea, and oxazoline analogues of SAHA. Bioorganic & Medicinal Chemistry Letters. 16: 4784-7. PMID 16870438 DOI: 10.1016/J.Bmcl.2006.06.090 |
0.301 |
|
2006 |
Hanessian S, Yang G, Rondeau JM, Neumann U, Betschart C, Tintelnot-Blomley M. Structure-based design and synthesis of macroheterocyclic peptidomimetic inhibitors of the aspartic protease beta-site amyloid precursor protein cleaving enzyme (BACE). Journal of Medicinal Chemistry. 49: 4544-67. PMID 16854060 DOI: 10.1021/Jm060154A |
0.384 |
|
2006 |
Hanessian S, Gauchet C, Charron G, Marin J, Nakache P. Design and synthesis of diversely substituted azacyclic inhibitors of endothelin converting enzyme. The Journal of Organic Chemistry. 71: 2760-78. PMID 16555831 DOI: 10.1021/Jo052649Y |
0.374 |
|
2006 |
Hanessian S, Therrien E, van Otterlo WA, Bayrakdarian M, Nilsson I, Fjellström O, Xue Y. Phenolic P2/P3 core motif as thrombin inhibitors--design, synthesis, and X-ray co-crystal structure. Bioorganic & Medicinal Chemistry Letters. 16: 1032-6. PMID 16290930 DOI: 10.1016/J.Bmcl.2005.10.082 |
0.768 |
|
2006 |
Hanessian S, Therrien E, Warrier JS, Charron G. Synthetic approaches to polyhydroxy indolizidines and related azabicyclic scaffolds Heterocycles. 70: 461-476. DOI: 10.3987/Com-06-S(W)44 |
0.368 |
|
2006 |
Hanessian S, Talbot C, Mauduit M, Saravanan P, Gone JR. From amino acids to polycyclic heterocycles-synthesis of enantiopure, functionally diverse isopavines and dihydromethanodibenzoazocines Heterocycles. 67: 205-214. DOI: 10.3987/Com-05-S(T)13 |
0.385 |
|
2006 |
Loiseleur O, Schneider H, Huang G, Machaalani R, Sellès P, Crowley P, Hanessian S. Synthesis of 1-Cytosinyl-N-malayamycin A Synfacts. 2006: 976-976. DOI: 10.1055/S-2006-949317 |
0.325 |
|
2006 |
Hanessian S, Giroux S, Mascitti V. The iterative synthesis of acyclic deoxypropionate units and their implication in polyketide-derived natural products Synthesis. 1057-1076. DOI: 10.1055/S-2006-926376 |
0.748 |
|
2006 |
Hanessian S, Talbot C, Saravanan P. Diastereoselective [3,2]-Stevens and Sommelet-Hauser rearrangements in the dihydromethanodibenzoazocine series Synthesis. 723-734. DOI: 10.1055/S-2006-926314 |
0.381 |
|
2006 |
Loiseleur O, Schneider H, Huang G, Machaalani R, Sellès P, Crowley P, Hanessian S. A scalable synthesis of 1-cytosinyl-N-malayamycin A: A potent fungicide Organic Process Research and Development. 10: 518-524. DOI: 10.1021/Op0600299 |
0.363 |
|
2006 |
Hanessian S, Del Valle JR, Xue Y, Blomberg N. Total Synthesis and Structural Confirmation of Chlorodysinosin A [J. Am. Chem. Soc.2006,128, 10491−10495]. Journal of the American Chemical Society. 128: 11727-11728. DOI: 10.1021/Ja069971Q |
0.356 |
|
2006 |
Hanessian S, Marcotte S, Machaalani R, Huang G, Pierron J, Loiseleur O. Total synthesis of malayamycin A and analogues Tetrahedron. 62: 5201-5214. DOI: 10.1016/J.Tet.2005.12.066 |
0.429 |
|
2005 |
Hanessian S, Kothakonda KK. Natural products as scaffolds for chemical diversification: solution-phase parallel synthesis of a series of naringin analogues. Journal of Combinatorial Chemistry. 7: 837-42. PMID 16283793 DOI: 10.1021/Cc0500351 |
0.351 |
|
2005 |
Hanessian S, Govindan S, Warrier JS. Probing the "additive effect" in the proline and proline hydroxamic acid catalyzed asymmetric addition of nitroalkanes to cyclic enones. Chirality. 17: 540-3. PMID 16189834 DOI: 10.1002/Chir.20201 |
0.369 |
|
2005 |
Hanessian S, Giroux S, Buffat M. Total synthesis and structural confirmation of (+)-longicin. Organic Letters. 7: 3989-92. PMID 16119949 DOI: 10.1021/Ol051483K |
0.786 |
|
2005 |
Hanessian S, Yun H, Hou Y, Tintelnot-Blomley M. Stereoselective synthesis of constrained azacyclic hydroxyethylene isosteres as aspartic protease inhibitors: dipolar cycloaddition and related methodologies toward branched pyrrolidine and pyrrolidinone carboxylic acids. The Journal of Organic Chemistry. 70: 6746-56. PMID 16095294 DOI: 10.1021/Jo050740W |
0.367 |
|
2005 |
Hanessian S, Hou Y, Bayrakdarian M, Tintelnot-Blomley M. Stereoselective synthesis of constrained oxacyclic hydroxyethylene isosteres of aspartic protease inhibitors: aldol and Mukaiyama aldol methodologies for branched tetrahydrofuran 2-carboxylic acids. The Journal of Organic Chemistry. 70: 6735-45. PMID 16095293 DOI: 10.1021/Jo050749Y |
0.79 |
|
2005 |
Hanessian S, Huang G, Chenel C, Machaalani R, Loiseleur O. Total synthesis of N-malayamycin A and related bicyclic purine and pyrimidine nucleosides. The Journal of Organic Chemistry. 70: 6721-34. PMID 16095292 DOI: 10.1021/Jo050727B |
0.383 |
|
2005 |
Hanessian S, Yun H, Hou Y, Yang G, Bayrakdarian M, Therrien E, Moitessier N, Roggo S, Veenstra S, Tintelnot-Blomley M, Rondeau JM, Ostermeier C, Strauss A, Ramage P, Paganetti P, et al. Structure-based design, synthesis, and memapsin 2 (BACE) inhibitory activity of carbocyclic and heterocyclic peptidomimetics. Journal of Medicinal Chemistry. 48: 5175-90. PMID 16078837 DOI: 10.1021/Jm050142+ |
0.786 |
|
2005 |
Hanessian S, Kothakonda KK. 3-N,N-Dimethylamino-3-deoxy lincomycin: a structure-based hybrid between lincomycin and the desosamine unit of erythromycin. Bioorganic & Medicinal Chemistry. 13: 5283-8. PMID 15994084 DOI: 10.1016/J.Bmc.2005.05.070 |
0.373 |
|
2005 |
Hanessian S, Tremblay M, Marzi M, Del Valle JR. Synthetic studies in the intramolecular carbocyclization of N-acyloxyiminium ions. Stereoelectronic and steric implications of nucleophilic alkene, alkyne, and allene tethers. The Journal of Organic Chemistry. 70: 5070-85. PMID 15960507 DOI: 10.1021/Jo050326W |
0.764 |
|
2005 |
Hanessian S, Kothakonda KK. Design and synthesis of oxazolidinone ketolide antibiotic segment mimetics Canadian Journal of Chemistry. 83: 801-811. DOI: 10.1139/V05-095 |
0.342 |
|
2005 |
Hanessian S, Machaalani R. Lewis acid mediated reductive ring opening of 2-methoxyethylidene acetals: A new approach to 2-methoxyethyl (MOE) ethers of cis-diols Synlett. 2437-2440. DOI: 10.1055/S-2005-872686 |
0.315 |
|
2004 |
Hanessian S, Tremblay M. Tandem functionalization of nonactivated alkenes and alkynes in intramolecular N-acyloxyiminium ion carbocyclization. Synthesis of 6-substituted hydroindole 2-carboxylic acids. Organic Letters. 6: 4683-6. PMID 15575660 DOI: 10.1021/Ol040053B |
0.617 |
|
2004 |
Hanessian S, Moitessier N. Sulfonamide-based acyclic and conformationally constrained MMP inhibitors: from computer-assisted design to nanomolar compounds. Current Topics in Medicinal Chemistry. 4: 1269-87. PMID 15320726 DOI: 10.2174/1568026043387953 |
0.321 |
|
2004 |
Hanessian S, Papeo G, Fettis K, Therrien E, Viet MT. Synthesis of 3 10-helix-inducing constrained analogues of L-proline. The Journal of Organic Chemistry. 69: 4891-9. PMID 15255713 DOI: 10.1021/Jo0401422 |
0.319 |
|
2004 |
Hanessian S, Mascitti V, Giroux S. Total synthesis of the cytotoxic cyclodepsipeptide (-)-doliculide: the "ester" effect in acyclic 1,3-induction of deoxypropionates. Proceedings of the National Academy of Sciences of the United States of America. 101: 11996-2001. PMID 15210988 DOI: 10.1073/Pnas.0401637101 |
0.78 |
|
2004 |
Hanessian S, Tremblay M, Petersen JF. The N-acyloxyiminium ion aza-Prins route to octahydroindoles: total synthesis and structural confirmation of the antithrombotic marine natural product oscillarin. Journal of the American Chemical Society. 126: 6064-71. PMID 15137772 DOI: 10.1021/Ja030669G |
0.617 |
|
2004 |
Hanessian S, Jnoff E, Bernstein N, Simard M. Bifunctional bis(oxazolines) as potential ligands in catalytic asymmetric reactions Canadian Journal of Chemistry. 82: 306-313. DOI: 10.1139/V03-198 |
0.357 |
|
2004 |
Hanessian S, Brassard M. Stereoselective synthesis of constrained oxacyclic hydroxyethylene isosteres of aspartyl protease inhibitors. Nitroaldol methodology toward 2,3-substituted tetrahydrofurans Tetrahedron. 60: 7621-7628. DOI: 10.1016/J.Tet.2004.06.060 |
0.417 |
|
2003 |
Hanessian S, Marcotte S, Machaalani R, Huang G. Total synthesis and structural confirmation of malayamycin A: a novel bicyclic C-nucleoside from Streptomyces malaysiensis. Organic Letters. 5: 4277-80. PMID 14601979 DOI: 10.1021/Ol030095K |
0.41 |
|
2003 |
Hanessian S, Yang Y, Giroux S, Mascitti V, Ma J, Raeppel F. Application of conformation design in acyclic stereoselection: total synthesis of borrelidin as the crystalline benzene solvate. Journal of the American Chemical Society. 125: 13784-92. PMID 14599218 DOI: 10.1021/Ja030139K |
0.804 |
|
2003 |
Hanessian S, Sailes H, Munro A, Therrien E. Synthesis of diversely functionalized indolizidinones and related bicyclic lactams using intramolecular Grubbs olefin metathesis and Dieckmann condensation. The Journal of Organic Chemistry. 68: 7219-33. PMID 12968870 DOI: 10.1021/Jo030145Z |
0.428 |
|
2003 |
Hanessian S, Papeo G, Angiolini M, Fettis K, Beretta M, Munro A. Synthesis of functionally diverse and conformationally constrained polycyclic analogues of proline and prolinol. The Journal of Organic Chemistry. 68: 7204-18. PMID 12968869 DOI: 10.1021/Jo0301447 |
0.416 |
|
2003 |
Hanessian S, Parthasarathy S, Mauduit M, Payza K. The power of visual imagery in drug design. Isopavines as a new class of morphinomimetics and their human opioid receptor binding activity. Journal of Medicinal Chemistry. 46: 34-48. PMID 12502358 DOI: 10.1021/Jm020164L |
0.349 |
|
2003 |
Hanessian S, Margarita R, Hall A, Johnstone S, Tremblay M, Parlanti L. New and old challenges in total synthesis. From concept to practice Pure and Applied Chemistry. 75: 209-221. DOI: 10.1351/Pac200375020209 |
0.629 |
|
2003 |
Hanessian S, Bayrakdarian M, Luo X. Total Synthesis of A-315675: A Potent Inhibitor of Influenza Neuraminidase. [J. Am. Chem. Soc.2002,124(17), 4716−4721]. Journal of the American Chemical Society. 125: 4958-4958. DOI: 10.1021/Ja0334457 |
0.306 |
|
2003 |
Hanessian S, Wang J, Montgomery D, Stoll V, Stewart KD, Kati W, Maring C, Kempt D, Hutchins C, Laver W. Corrigendum to ‘Design, Synthesis, and Neuraminidase Inhibitory Activity of GS-4071 Analogues that Utilize a Novel Hydrophobic Paradigm’ Bioorganic & Medicinal Chemistry Letters. 13: 1837. DOI: 10.1016/S0960-894X(03)00300-7 |
0.4 |
|
2003 |
Hanessian S, Sailes H, Therrien E. Synthesis of functionally diverse bicyclic sulfonamides as constrained proline analogues and application to the design of potential thrombin inhibitors Tetrahedron. 59: 7047-7056. DOI: 10.1016/S0040-4020(03)00919-0 |
0.424 |
|
2003 |
Hanessian S, Kornienko A, Swayze EE. Probing the functional requirements of the L-haba side-chain of amikacin - Synthesis, 16S A-site rRNA binding, and antibacterial activity Tetrahedron. 59: 995-1007. DOI: 10.1016/S0040-4020(02)01625-3 |
0.358 |
|
2003 |
Hanessian S, Tremblay M, Swayze EE. Tobramycin analogues with C-5 aminoalkyl ether chains intended to mimic rings III and IV of paromomycin Tetrahedron. 59: 983-993. DOI: 10.1016/S0040-4020(02)01624-1 |
0.607 |
|
2003 |
Hanessian S, Machaalani R. A highly stereocontrolled and efficient synthesis of α- and β-pseudouridines Tetrahedron Letters. 44: 8321-8323. DOI: 10.1016/J.Tetlet.2003.09.103 |
0.347 |
|
2003 |
Saladino R, Ciambecchini U, Hanessian S. Synthesis of 1′-Homo-N-nucleosides from Hexitols European Journal of Organic Chemistry. 4401-4405. DOI: 10.1002/Ejoc.200300328 |
0.387 |
|
2002 |
Hanessian S, Wang J, Montgomery D, Stoll V, Stewart KD, Kati W, Maring C, Kempf D, Hutchins C, Laver WG. Design, synthesis, and neuraminidase inhibitory activity of GS-4071 analogues that utilize a novel hydrophobic paradigm. Bioorganic & Medicinal Chemistry Letters. 12: 3425-9. PMID 12419376 DOI: 10.1016/S0960-894X(02)00732-1 |
0.381 |
|
2002 |
Hanessian S, Margarita R, Hall A, Johnstone S, Tremblay M, Parlanti L. Total synthesis and structural confirmation of the marine natural product Dysinosin A: a novel inhibitor of thrombin and Factor VIIa. Journal of the American Chemical Society. 124: 13342-3. PMID 12418860 DOI: 10.1021/Ja0208153 |
0.64 |
|
2002 |
Hanessian S, Therrien E, Granberg K, Nilsson I. Targeting thrombin and factor VIIa: design, synthesis, and inhibitory activity of functionally relevant indolizidinones. Bioorganic & Medicinal Chemistry Letters. 12: 2907-11. PMID 12270173 DOI: 10.1016/S0960-894X(02)00612-1 |
0.331 |
|
2002 |
Hanessian S, Claridge S, Johnstone S. The power of visual imagery in synthesis planning. Stereocontrolled approaches to CGP-60536B, a potent renin inhibitor. The Journal of Organic Chemistry. 67: 4261-74. PMID 12054962 DOI: 10.1021/Jo011184I |
0.4 |
|
2002 |
Hanessian S, Buckle R, Bayrakdarian M. Design and synthesis of a novel class of constrained tricyclic pyrrolizidinone carboxylic acids as carbapenem mimics. The Journal of Organic Chemistry. 67: 3387-97. PMID 12003550 DOI: 10.1021/Jo0111715 |
0.793 |
|
2002 |
Hanessian S, Mascitti V, Rogel O. Synthesis of a potent antagonist of E-selectin. The Journal of Organic Chemistry. 67: 3346-54. PMID 12003545 DOI: 10.1021/Jo0110956 |
0.366 |
|
2002 |
Hanessian S, Bayrakdarian M, Luo X. Total synthesis of A-315675: a potent inhibitor of influenza neuraminidase. Journal of the American Chemical Society. 124: 4716-21. PMID 11971721 DOI: 10.1021/Ja0126226 |
0.797 |
|
2002 |
Hanessian S, Angiolini M. Conformationally stable and constrained macrocarbocyclic pseudopeptide mimics of beta-hairpin structures. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 111-7. PMID 11822444 DOI: 10.1002/1521-3765(20020104)8:1<111::Aid-Chem111>3.0.Co;2-S |
0.372 |
|
2002 |
Hanessian S, Jnoff E, Griffin AM. Penicillamine as a ligand in the catalytic asymmetric reduction of ketones Canadian Journal of Chemistry. 80: 885-888. DOI: 10.1139/V01-174 |
0.328 |
|
2002 |
Hanessian S, Mascitti V, Lu PP, Ishida H. One-step stereocontrolled synthesis of α-anomeric carboxylic acid esters from unprotected glycosyl donors: A water-soluble aspirin pro-drug analogue Synthesis. 1959-1968. DOI: 10.1055/S-2002-34372 |
0.338 |
|
2002 |
Hanessian S, Ma J, Wang W, Gai Y. Total Synthesis of Bafilomycin A1Relying on Iterative 1,2-Induction in Acyclic Precursors [J. Am.Chem. Soc.2001,123, 10200−10206]. Journal of the American Chemical Society. 124: 7249-7249. DOI: 10.1021/Ja025105B |
0.52 |
|
2002 |
Hanessian S, Bayrakdarian M. Solution- and solid-phase asymmetric synthesis of substituted N-hydroxypyrrolidine dicarboxylic acids Tetrahedron Letters. 43: 9441-9444. DOI: 10.1016/S0040-4039(02)02288-8 |
0.787 |
|
2002 |
Hanessian S, Van Otterlo WAL, Nilsson I, Bauer U. Stereocontrolled synthesis of a prototype library of enantiopure 2,4-disubstituted 4-aryl-6-piperidinones and piperidines Tetrahedron Letters. 43: 1995-1998. DOI: 10.1016/S0040-4039(02)00184-3 |
0.35 |
|
2002 |
Hanessian S, Seid M, Nilsson I. Stereocontrolled synthesis of enantiopure diversely functionalized prototypical piperidinone libraries, and constrained analogs of 4-substituted 2-amino adipic acid Tetrahedron Letters. 43: 1991-1994. DOI: 10.1016/S0040-4039(02)00183-1 |
0.397 |
|
2002 |
Hanessian S, Bayrakdarian M. Asymmetric synthesis of diversely substituted N-hydroxypyrrolidines using cycloadditions with chiral nitrone enolate/ylids Tetrahedron Letters. 43: 967-971. DOI: 10.1016/S0040-4039(01)02305-X |
0.794 |
|
2002 |
Hanessian S, Compain P. Corrigendum to “Lewis acid promoted cyclocondensations of α-ketophosphonoenoates with dienes—from Diels–Alder to hetero Diels–Alder reactions” Tetrahedron. 58: 10087. DOI: 10.1016/S0040-4020(02)01353-4 |
0.59 |
|
2002 |
Hanessian S, Compain P. Lewis acid promoted cyclocondensations of alpha;-ketophosphonoenoates with dienes - From Diels-Alder to hetero Diels-Alder reactions Tetrahedron. 58: 6521-6529. DOI: 10.1016/S0040-4020(02)00662-2 |
0.614 |
|
2002 |
Hanessian S, Mauduit M, Demont E, Talbot C. Synthesis of desymmetrized, enantiopure dihydro-methano-diarylazocines: Topologically interesting eyeteaser molecules Tetrahedron. 58: 1485-1490. DOI: 10.1016/S0040-4020(02)00012-1 |
0.371 |
|
2001 |
Hanessian S, Ma J, Wang W, Gai Y. Total synthesis of bafilomycin A(1) relying on iterative 1,2-induction in acyclic precursors. Journal of the American Chemical Society. 123: 10200-6. PMID 11603969 DOI: 10.1021/Ja011452U |
0.556 |
|
2001 |
Hanessian S, Fu JM. Total synthesis of polyoximic acid Canadian Journal of Chemistry. 79: 1812-1826. DOI: 10.1139/V01-171 |
0.387 |
|
2001 |
Hanessian S, Ma J. From glyceraldehyde to functionalized enantiopure tetrahydronaphthalenes and indanes Tetrahedron Letters. 42: 8785-8788. DOI: 10.1016/S0040-4039(01)01914-1 |
0.513 |
|
2001 |
Hanessian S, Moitessier N, Cantin LD. Design and synthesis of MMP inhibitors using N-arylsulfonylaziridine hydroxamic acids as constrained scaffolds Tetrahedron. 57: 6885-6900. DOI: 10.1016/S0040-4020(01)00641-X |
0.688 |
|
2001 |
Hanessian S, Huynh HK, Reddy GV, Duthaler RO, Katopodis A, Streiff MB, Kinzy W, Oehrlein R. Synthesis of Gal determinant epitopes, their glycomimetic variants, and trimeric clusters - Relevance to tumor associated antigens and to discordant xenografts Tetrahedron. 57: 3281-3290. DOI: 10.1016/S0040-4020(01)00195-8 |
0.676 |
|
2001 |
Hanessian S, Tremblay M, Kornienko A, Moitessier N. Design, modeling and synthesis of functionalized paromamine analogs Tetrahedron. 57: 3255-3265. DOI: 10.1016/S0040-4020(01)00194-6 |
0.61 |
|
2000 |
Hanessian S, Gomtsyan A, Malek N. Asymmetric conjugate additions of chiral phosphonamide anions to alpha,beta-unsaturated carbonyl compounds. A versatile method for vicinally substituted chirons The Journal of Organic Chemistry. 65: 5623-31. PMID 10970301 DOI: 10.1021/Jo000388G |
0.388 |
|
2000 |
Hanessian S, Griffin AM, Cantin LD. Asymmetric synthesis of functionalized carbocycles and heterocycles. Chirality. 12: 342-5. PMID 10824149 DOI: 10.1002/(Sici)1520-636X(2000)12:5/6<342::Aid-Chir7>3.0.Co;2-Y |
0.699 |
|
2000 |
Hanessian S, Rogel O. Synthesis of glycophostones: cyclic phosphonate analogues of biologically relevant sugars The Journal of Organic Chemistry. 65: 2667-74. PMID 10808439 DOI: 10.1021/Jo991696L |
0.344 |
|
2000 |
Hanessian S, Sgarbi PW. Design and synthesis of mimics of S-adenosyl-L-homocysteine as potential inhibitors of erythromycin methyltransferases. Bioorganic & Medicinal Chemistry Letters. 10: 433-7. PMID 10743942 DOI: 10.1016/S0960-894X(00)00021-4 |
0.364 |
|
2000 |
Hanessian S, Bayrakdarian M. Pyrrolidine as a cogwheel-like scaffold for the deployment of diverse functionality through cycloaddition reactions of metallo-1,3-dipoles in aqueous media. Bioorganic & Medicinal Chemistry Letters. 10: 427-31. PMID 10743941 DOI: 10.1016/S0960-894X(00)00020-2 |
0.752 |
|
2000 |
Hanessian S, Balaux E, Musil D, Olsson LL, Nilsson I. Exploring the chiral space within the active site of alpha-thrombin with a constrained mimic of D-Phe-Pro-Arg--design, synthesis, inhibitory activity, and X-ray structure of an enzyme-inhibitor complex. Bioorganic & Medicinal Chemistry Letters. 10: 243-7. PMID 10698445 DOI: 10.1016/S0960-894X(99)00669-1 |
0.349 |
|
2000 |
Hanessian S, Sharma R. The synthesis of bicyclic piperazine-2-carboxylic acids from L-proline Heterocycles. 52: 1231-1239. DOI: 10.3987/Com-99-S136 |
0.351 |
|
2000 |
Hanessian S, Cantin LD. The synthesis of enantiomerically pure disubstituted aziridines and N- alkoxy aziridines Tetrahedron Letters. 41: 787-790. DOI: 10.1016/S0040-4039(99)02211-X |
0.683 |
|
2000 |
Hanessian S, Demont E, Van Otterlo WAL. From serine to functionalized enantiopure tetrahydroisoquinolines Tetrahedron Letters. 41: 4999-5003. DOI: 10.1016/S0040-4039(00)00765-6 |
0.381 |
|
2000 |
Hanessian S, Moitessier N, Wilmouth S. Tetrahydrofuran as a scaffold for peptidomimetics. Application to the design and synthesis of conformationally constrained metalloproteinase inhibitors Tetrahedron. 56: 7643-7660. DOI: 10.1016/S0040-4020(00)00687-6 |
0.339 |
|
1999 |
Hanessian S, McNaughton-Smith G. Synthesis of a versatile peptidomimetic scaffold. Methods in Molecular Medicine. 23: 161-174. PMID 21380897 DOI: 10.1385/0-89603-517-4:161 |
0.347 |
|
1999 |
Hanessian S, Cantin LD, Andreotti D. Total Synthesis and Absolute Configuration of (-)-Anthoplalone. The Journal of Organic Chemistry. 64: 4893-4900. PMID 11674567 DOI: 10.1021/Jo990302N |
0.705 |
|
1999 |
Hanessian S, Rogel O. Synthesis of a phostone glycomimetic of the endothelin converting enzyme inhibitor phosphoramidon Bioorganic and Medicinal Chemistry Letters. 9: 2441-2446. PMID 10476884 DOI: 10.1016/S0960-894X(99)00401-1 |
0.324 |
|
1999 |
Hanessian S, Bernstein N, Yang RY, Maguire R. Asymmetric synthesis of L-azetidine-2-carboxylic acid and 3-substituted congeners--conformationally constrained analogs of phenylalanine, naphthylalanine, and leucine. Bioorganic & Medicinal Chemistry Letters. 9: 1437-42. PMID 10360752 DOI: 10.1016/S0960-894X(99)00218-8 |
0.354 |
|
1999 |
Hanessian S, Reinhold U, Saulnier M, Claridge S. Probing the importance of spacial and conformational domains in captopril analogs for angiotensin converting enzyme activity. Bioorganic & Medicinal Chemistry Letters. 8: 2123-8. PMID 9873498 DOI: 10.1016/S0960-894X(98)00377-1 |
0.325 |
|
1999 |
Hanessian S, Johnstone S. Synthesis of Hydroxamic Esters via Alkoxyaminocarbonylation of β-Dicarbonyl Compounds Journal of Organic Chemistry. 64: 5896-5903. DOI: 10.1021/Jo990353K |
0.332 |
|
1999 |
Hanessian S, Luo X, Schaum R. Synthesis and folding preferences of γ-amino acid oligopeptides: stereochemical control in the formation of a reverse turn and a helix Tetrahedron Letters. 40: 4925-4929. DOI: 10.1016/S0040-4039(99)00860-6 |
0.354 |
|
1999 |
Hanessian S, Ma J, Wang W. One- and two-directional iterative 1,2-asymmetric induction in acyclic systems—easy access to anti,anti and anti,syn dipropionate and diphenylacetate stereotriads Tetrahedron Letters. 40: 4627-4630. DOI: 10.1016/S0040-4039(99)00783-2 |
0.503 |
|
1999 |
Hanessian S, Ma J, Wang W. Stereocontrolled solution and solid phase enolate alkylations and hydroxylations — generation of three and four contiguous stereogenic carbon atoms in acyclic systems Tetrahedron Letters. 40: 4631-4634. DOI: 10.1016/S0040-4039(99)00782-0 |
0.49 |
|
1999 |
Hanessian S, Huynh HK. Solution and solid phase p-alkoxybenzylation of alcohols under neutral conditions Tetrahedron Letters. 40: 671-674. DOI: 10.1016/S0040-4039(98)02531-3 |
0.655 |
|
1999 |
Hanessian S, Reddy B. Total synthesis of tricyclic ?-lactams Tetrahedron. 55: 3427-3443. DOI: 10.1016/S0040-4020(98)01152-1 |
0.439 |
|
1998 |
Hanessian S, Huynh HK, Reddy GV, McNaughton-Smith G, Ernst B, Kolb HC, Magnani J, Sweeley C. Exploration of beta-turn scaffolding motifs as components of sialyl Le(X) mimetics and their relevance to P-selectin. Bioorganic & Medicinal Chemistry Letters. 8: 2803-8. PMID 9873626 DOI: 10.1016/S0960-894X(98)00500-9 |
0.666 |
|
1998 |
Hanessian S, Grillo TA. Stereocontrolled Total Synthesis of an Annonacin A-Type Acetogenin: Pseudoannonacin A?† Journal of Organic Chemistry. 63: 1049-1057. DOI: 10.1021/Jo9713621 |
0.395 |
|
1998 |
Hanessian S, Lu P, Ishida H. One-Step, Stereocontrolled Synthesis of Glycosyl 1-Phosphates, Uridine-5‘-diphosphogalactose, and Uridine-5‘-diphosphoglucose from Unprotected Glycosyl Donors Journal of the American Chemical Society. 120: 13296-13300. DOI: 10.1021/Ja982783I |
0.342 |
|
1998 |
Hanessian S, Margarita R. 1,3-Asymmetric induction in dianionic allylation reactions of amino acid derivatives-synthesis of functionally useful enantiopure glutamates, pipecolates and pyroglutamates Tetrahedron Letters. 39: 5887-5890. DOI: 10.1016/S0040-4039(98)00900-9 |
0.385 |
|
1998 |
Hanessian S, Margarita R, Hall A, Luo X. 1,2-Asymmetric induction in dianionic allylation reactions of amino acid derivatives-synthesis of functionally useful, enantiopure aspartates and constrained scaffolds Tetrahedron Letters. 39: 5883-5886. DOI: 10.1016/S0040-4039(98)00899-5 |
0.402 |
|
1998 |
Hanessian S, Xie F. Exploring functional and molecular diversity with polymer-bound p-alkoxybenzyl ethers - Scope and applicaitons of preparatively useful organic reactions Tetrahedron Letters. 39: 737-740. DOI: 10.1016/S0040-4039(97)10685-2 |
0.309 |
|
1998 |
Hanessian S, Cantin L. Synthesis and Biological Evaluation of Constrained Phosphonoglutamic Acids as Metabotropic Agents Molecules Online. 2: 46-52. DOI: 10.1007/S007830050054 |
0.699 |
|
1997 |
Bennani YL, Hanessian S. trans-1,2-Diaminocyclohexane Derivatives as Chiral Reagents, Scaffolds, and Ligands for Catalysis: Applications in Asymmetric Synthesis and Molecular Recognition. Chemical Reviews. 97: 3161-3196. PMID 11851488 DOI: 10.1021/Cr9407577 |
0.364 |
|
1997 |
Hanessian S, Pan J, Carnell A, Bouchard H, Lesage L. Total Synthesis of (-)-Reserpine Using the Chiron Approach. The Journal of Organic Chemistry. 62: 465-473. PMID 11671435 DOI: 10.1021/Jo961713W |
0.434 |
|
1997 |
Hanessian S, Yang R, Sancéau J. Synthesis of 1-N-hydroxyhydantoin 5-phosphates as potential fungicides Canadian Journal of Chemistry. 75: 712-715. DOI: 10.1139/V97-085 |
0.384 |
|
1997 |
Hanessian S, Park H, Yang R. Zinc-Mediated Allylation of N-Protected α-Amino Aldehydes in Aqueous Solution. Stereoselective Synthesis of Anti- and Syn-β-Amino Alcohols with Functionalized Allyl Groups Synlett. 1997: 353-354. DOI: 10.1055/S-1997-804 |
0.35 |
|
1997 |
Hanessian S, Park H, Yang R. Zinc-Mediated Allylation of N-Protected α-Amino Aldehydes in Aqueous Solution. Stereoselective Synthesis of Phe-Phe Hydroxyethylene Dipeptide Isosteres Synlett. 1997: 351-352. DOI: 10.1055/S-1997-803 |
0.358 |
|
1997 |
Hanessian S, Wang W, Gai Y, Olivier E. A General and Stereocontrolled Strategy for the Iterative Assembly of Enantiopure Polypropionate Subunits: Synthesis of the C19−C28 Segment of Rifamycin S from a Single Chiron Journal of the American Chemical Society. 119: 10034-10041. DOI: 10.1021/Ja970251G |
0.348 |
|
1997 |
Hanessian S, Griffin A, Devasthale PV. Synthesis of conformationally constrained potential inhibitors of mammalian metalloproteinases Bioorganic & Medicinal Chemistry Letters. 7: 3119-3124. DOI: 10.1016/S0960-894X(97)10171-8 |
0.394 |
|
1997 |
Hanessian S, Reddy GV, Huynh HK, Jingwen P, Pedatella S, Ernst B, Kolb HC. Design and synthesis of sialyl Le(x) mimetics based on carbocyclic scaffolds derived from (-)-quinic acid Bioorganic and Medicinal Chemistry Letters. 7: 2729-2734. DOI: 10.1016/S0960-894X(97)10077-4 |
0.708 |
|
1997 |
Hanessian S, Griffin AM, Rozema MJ. Tricyclic β-lactams: Total synthesis and antibacterial activity of 5α-methoxyethyl and 5α-hydroxyethyl trinems Bioorganic and Medicinal Chemistry Letters. 7: 1857-1862. DOI: 10.1016/S0960-894X(97)00326-0 |
0.722 |
|
1997 |
Hanessian S, Yang H. Design of a novel secondary structure scaffolding device: Induction of a reverse turn in tetrapeptides by incorporating a β-amino acid and stereocontrolled free radical α-substitution reactions in peptide motifs Tetrahedron Letters. 38: 3155-3158. DOI: 10.1016/S0040-4039(97)00612-6 |
0.332 |
|
1997 |
Hanessian S, Cantin L, Roy S, Andreotti D, Gomtsyan A. The synthesis of enantiomerically pure, symmetrically substituted cyclopropane phosphonic acids — A constrained analog of the GABA antagonist phaclophen Tetrahedron Letters. 38: 1103-1106. DOI: 10.1016/S0040-4039(96)02518-X |
0.697 |
|
1997 |
Hanessian S, Schaum R. 1,3-Asymmetric induction in enolate alkylation reactions of N-protected γ-amino acid derivatives Tetrahedron Letters. 38: 163-166. DOI: 10.1016/S0040-4039(96)02263-0 |
0.352 |
|
1997 |
Hanessian S, McNaughton-Smith G, Lombart H, Lubell WD. Design and synthesis of conformationally constrained amino acids as versatile scaffolds and peptide mimetics Tetrahedron. 53: 12789-12854. DOI: 10.1016/S0040-4020(97)00476-6 |
0.309 |
|
1997 |
Hanessian S, Abad-Grillo T, McNaughton-Smith G. Synthesis of (4S)-hydroxymethyl-(2R)-(2-propyl)-butyrolactone: A quest for a practical route to an important hydroxyethylene isostere chiron Tetrahedron. 53: 6281-6294. DOI: 10.1016/S0040-4020(97)00298-6 |
0.307 |
|
1997 |
Hanessian S, Reinhold U, Gentile G. The Synthesis of Enantiopure ω‐Methanoprolines and ω‐Methanopipecolic Acids by a Novel Cyclopropanation Reaction: The “Flattering” of Proline Angewandte Chemie. 36: 1881-1884. DOI: 10.1002/Anie.199718811 |
0.377 |
|
1996 |
Hanessian S, Ninkovic S. Total synthesis of isodeoxypodophyllotoxin using the Me3Sn radical initiated carbocyclization Canadian Journal of Chemistry. 74: 1880-1888. DOI: 10.1139/V96-211 |
0.33 |
|
1996 |
Hanessian S, Qiu D, Prabhanjan H, Reddy GV, Lou B. Synthesis of clustered D-GalNAc (Tn) and D-Galβ(1→3)GalNAc (T) antigenic motifs using a pentaerythritol scaffold Canadian Journal of Chemistry. 74: 1738-1747. DOI: 10.1139/V96-192 |
0.306 |
|
1996 |
Hanessian S, Prabhanjan H, Qiu D, Nambiar S. Synthesis of chemically and functionally diverse scaffolds from pentaerythritol Canadian Journal of Chemistry. 74: 1731-1737. DOI: 10.1139/V96-191 |
0.394 |
|
1996 |
Hanessian S, Sancéau J. Asymmetric synthesis of taxol arid taxotère side chains by enolate hydroxylation Canadian Journal of Chemistry. 74: 621-624. DOI: 10.1139/V96-066 |
0.376 |
|
1996 |
Hanessian S, Ninkovic S. Stereoselective Synthesis of (−)-α-Kainic Acid and (+)-α-Allokainic Acid via Trimethylstannyl-Mediated Radical Carbocyclization and Oxidative Destannylation Journal of Organic Chemistry. 61: 5418-5424. DOI: 10.1021/Jo9604088 |
0.329 |
|
1996 |
Hanessian S, Andreotti aD, Gomtsyan A. Asymmetric Synthesis of Enantiomerically Pure and Diversely Functionalized Cyclopropanes J. Am. Chem. Soc. 1995, 117, 10393−10394 Journal of the American Chemical Society. 118: 2537-2537. DOI: 10.1021/Ja955040V |
0.362 |
|
1996 |
Hanessian S, McNaughton-Smith G. A versatile synthesis of a β-turn peptidomimetic scaffold: An approach towards a designed model antagonist of the tachykinin NK-2 receptor Bioorganic & Medicinal Chemistry Letters. 6: 1567-1572. DOI: 10.1016/S0960-894X(96)00275-2 |
0.376 |
|
1996 |
Hanessian S, Tehim A, Meng Q, Granberg K. A remarkably facile and stereochemically controlled fragmentation reaction in the hygrolide group of macrolide antibiotics Tetrahedron Letters. 37: 9001-9004. DOI: 10.1016/S0040-4039(96)02113-2 |
0.362 |
|
1996 |
Hanessian S, Yang R. Enantioselective allylation of α-ketoester oximes with an external chiral ligand: Asymmetric synthesis of allylglycines and allylalanine Tetrahedron Letters. 37: 8997-9000. DOI: 10.1016/S0040-4039(96)02112-0 |
0.384 |
|
1996 |
Hanessian S, Ninkovic S, Reinhold U. The synthesis of 4,5-methano congeners of α-kainic and α-allo-kainic acids as probes for glutamate receptors Tetrahedron Letters. 37: 8971-8974. DOI: 10.1016/S0040-4039(96)02105-3 |
0.373 |
|
1996 |
Hanessian S, Reinhold U, Ninkovic S. The stereocontrolled synthesis of enantiopure α-methano heterocycles and constrained amino acid analogs Tetrahedron Letters. 37: 8967-8970. DOI: 10.1016/S0040-4039(96)02104-1 |
0.363 |
|
1996 |
Hanessian S, Devasthale PV. Design and synthesis of novel, pseudo C2 symmetric inhibitors of HIV protease Bioorganic & Medicinal Chemistry Letters. 6: 2201-2206. DOI: 10.1016/0960-894X(96)00392-7 |
0.336 |
|
1996 |
Hanessian S, Wang W, Gai Y. Stereocontrolled sequential functionalization in acyclic systems by exploiting internal 1,2-asymmetric induction — generation of symmetry-related polyamino alcohol motifs Tetrahedron Letters. 37: 7477-7480. DOI: 10.1016/0040-4039(96)01754-6 |
0.346 |
|
1996 |
Hanessian S, Gai Y, Wang W. Stereocontrolled Functionalization In Acyclic Systems By Exploiting Internal 1,2-Asymmetric Induction-Generation Of Polypropionate And Related Motifs Tetrahedron Letters. 37: 7473-7476. DOI: 10.1016/0040-4039(96)01753-4 |
0.335 |
|
1996 |
Hanessian S, Yang R. Solution and solid phase synthesis of 5-alkoxyhydantoin libraries with a three-fold functional diversity Tetrahedron Letters. 37: 5835-5838. DOI: 10.1016/0040-4039(96)01244-0 |
0.332 |
|
1996 |
Hanessian S, Yang R. The asymmetric synthesis of allylglycine and other unnatural α-amino acids via zinc-mediated allylation of oximes in aqueous media Tetrahedron Letters. 37: 5273-5276. DOI: 10.1016/0040-4039(96)01118-5 |
0.391 |
|
1996 |
Hanessian S, Devasthale PV. Generation of functional diversity via nitroaldol condensations of α-aminoacid aldehydes — A new and stereocontrolled route to acyclic 1,3-diamino-2-alcohols Tetrahedron Letters. 37: 987-990. DOI: 10.1016/0040-4039(95)02359-3 |
0.36 |
|
1996 |
Bennani YL, Hanessian S. The asymmetric synthesis of α-substituted α-methyl and α-phenyl phosphonic acids: Design, carbanion geometry, reactivity and preparative aspects of chiral alkyl bicyclic phosphonamides Tetrahedron. 52: 13837-13866. DOI: 10.1016/0040-4020(96)00829-0 |
0.345 |
|
1996 |
Vatèle J, Hanessian S. Design and reactivity of organic functional groups - preparation and nucleophilic displacement reactions of imidazole-1-sulfonates (imidazylates) Tetrahedron. 52: 10557-10568. DOI: 10.1016/0040-4020(96)00586-8 |
0.355 |
|
1995 |
Hanessian S, Yang R. Synthesis of N-Hydroxy α-Amino Acids from α-Hydroxy Acids with High Enantiomeric Purity Synlett. 1995: 633-634. DOI: 10.1055/S-1995-5031 |
0.331 |
|
1995 |
Hanessian S, Benalil A, Laferriere C. The Synthesis of Functionalized Cyclodextrins As Scaffolds and Templates for Molecular Diversity, Catalysis, and Inclusion Phenomena The Journal of Organic Chemistry. 60: 4786-4797. DOI: 10.1021/Jo00120A023 |
0.358 |
|
1995 |
Hanessian S, Andreotti D, Gomtsyan A. Asymmetric synthesis of enantiomerically pure and diversely functionalized cyclopropanes. Journal of the American Chemical Society. 117: 10393-10394. DOI: 10.1021/Ja00146A029 |
0.396 |
|
1995 |
Hanessian S, Rozema MJ, Reddy GB, Braganza JF. Tricyclic β-lactams: total synthesis and antibacterial activity of 5α- and 5β-methoxy-tribactams Bioorganic and Medicinal Chemistry Letters. 5: 2535-2540. DOI: 10.1016/0960-894X(95)00445-Y |
0.72 |
|
1995 |
Hanessian S, Condé JJ, Lou B. The stereocontrolled synthesis of 1,2-cis furanosyl nucleosides via a novel anomeric activation Tetrahedron Letters. 36: 5865-5868. DOI: 10.1016/0040-4020(96)00611-4 |
0.344 |
|
1995 |
Hanessian S, Benalil A, Simard M, Bélanger-Gariépy F. Crystal structures and molecular conformations of mono-6-azido-6-deoxy α-Cyclodextrin and mono-2-O-allyl-α-cyclodextrin -The formation of polymeric helical inclusion complexes Tetrahedron. 51: 10149-10158. DOI: 10.1016/0040-4020(95)00609-C |
0.313 |
|
1995 |
Hanessian S, Benalil A, Viet MTP. The intramolecular inclusion of aromatic esters within β-cyclodextrin as a function of chain length — a detailed NMR study Tetrahedron. 51: 10131-10148. DOI: 10.1016/0040-4020(95)00608-B |
0.323 |
|
1995 |
Hanessian S, Sancéau J, Chemla P. Synthesis of surrogate structures related to the herbicidal agent hydantocidin Tetrahedron. 51: 6669-6678. DOI: 10.1016/0040-4020(95)00324-2 |
0.407 |
|
1994 |
Hanessian S, Bennani YL. Electrophilic Amination and Azidation of Chiral α-Alkyl Phosphonamides: Asymmetric Syntheses of α-Amino α-Alkyl Phosphonic Acids† Synthesis. 1994: 1272-1274. DOI: 10.1055/S-1994-25679 |
0.319 |
|
1994 |
Hanessian S, Girard C. One Step α-Deoxygenation of Unprotected Aldonolactones using Samarium Diiodide-THF/H2O System - A New Synthesis of 2-Deoxy-D-Ribose Synlett. 1994: 861-862. DOI: 10.1055/S-1994-23034 |
0.349 |
|
1994 |
Hanessian S, Gomtsyan A, Payne A, Herve Y. Asymmetric conjugate additions of chiral allyl- and crotylphosphonamide anions to .alpha.,.beta.-unsaturated carbonyl compounds: highly stereocontrolled access to vicinally substituted carbon centers and chemically asymmetrized chirons. [Erratum to document cited in CA119:250032] Journal of Organic Chemistry. 59: 3242-3242. DOI: 10.1021/Jo00090A055 |
0.322 |
|
1994 |
Hanessian S, Galéotti N, Rosen P, Oliva G, Babu S. Synthesis of carbohydrate phostones as potential glycomimetics Bioorganic & Medicinal Chemistry Letters. 4: 2763-2768. DOI: 10.1016/S0960-894X(01)80591-6 |
0.358 |
|
1994 |
Hanessian S, Raghavan S. Design and synthesis of a prototypical non-peptidic inhibitor model for the enzme renin Bioorganic and Medicinal Chemistry Letters. 4: 1697-1702. DOI: 10.1016/S0960-894X(00)80364-9 |
0.32 |
|
1994 |
Hanessian S, Gomtsyan A. Highly stereocontrolled sequential asymmetric Michael addition reactions with cinnamate esters - generation of three and four contiguous stereogenic centers on seven-carbon acyclic motifs Tetrahedron Letters. 35: 7509-7512. DOI: 10.1016/S0040-4039(00)78330-4 |
0.362 |
|
1994 |
Hanessian S, Meng Q, Olivier E. An unprecedented ring expansion in the Macrolide series - synthesis of iso-bafilomycin A1 Tetrahedron Letters. 35: 5393-5396. DOI: 10.1016/S0040-4039(00)73508-8 |
0.375 |
|
1994 |
Hanessian S, Reddy G. Synthesis of tricyclic β-lactams - functionally and topologically novel carbacephems Bioorganic & Medicinal Chemistry Letters. 4: 2285-2290. DOI: 10.1016/0960-894X(94)85026-7 |
0.389 |
|
1994 |
Hanessian S, Rozema MJ. Synthesis and biological evaluation of 1-substituted-7-(1-hydroxyethyl) carbacephems - a class of "hybrid" bicyclic β-lactams Bioorganic and Medicinal Chemistry Letters. 4: 2279-2284. DOI: 10.1016/0960-894X(94)85025-9 |
0.748 |
|
1993 |
Hanessian S, Bennani YL, Leblanc Y. Efficient olefination with α-alkyl cyclic phosphonamides Heterocycles. 35: 1411-1424. DOI: 10.3987/Com-93-S(T)145 |
0.358 |
|
1993 |
Hanessian S. Reflections on the total synthesis of natural products: Art, craft, logic, and the chiron approach Pure and Applied Chemistry. 65: 1189-1204. DOI: 10.1351/Pac199365061189 |
0.362 |
|
1993 |
Hanessian S, Vanasse B, Yang H, Alpegiani M. Highly stereocontrolled syntheses of 2,3-disubstituted 1,4-butyrolactones using ionic and free radical reactions Canadian Journal of Chemistry. 71: 1407-1411. DOI: 10.1139/V93-182 |
0.304 |
|
1993 |
Hanessian S, Wang J. Synthesis and biological evaluation of novel chiral non-racemic diaminoplatinum analogs based on a tetrahydropyran motif Canadian Journal of Chemistry. 71: 886-895. DOI: 10.1139/V93-118 |
0.388 |
|
1993 |
Hanessian S, Gauthier J, Okamoto K, Beauchamp A, Theophanides T. Synthesis of diaminodideoxyalditol analogs of cisplatin as antitumor agents Canadian Journal of Chemistry. 71: 880-885. DOI: 10.1139/V93-117 |
0.323 |
|
1993 |
Hanessian S, Bennani YL, Hervé Y. A Novel Asymmetric Synthesis of α- and β-Amino Aryl Phosphonic Acids Synlett. 1993: 35-36. DOI: 10.1055/S-1993-22337 |
0.35 |
|
1993 |
Hanessian S, Tehim A, Chen P. Total synthesis of (-)-tetrahydrolipstatin Journal of Organic Chemistry. 58: 7768-7781. DOI: 10.1021/Jo00079A022 |
0.414 |
|
1993 |
Hanessian S, Gomtsyan A, Payne A, Herve Y, Beaudoin S. Asymmetric conjugate additions of chiral allyl- and crotylphosphonamide anions to .alpha.,.beta.-unsaturated carbonyl compounds: highly stereocontrolled access to vicinally substituted carbon centers and chemically asymmetrized chirons Journal of Organic Chemistry. 58: 5032-5034. DOI: 10.1021/Jo00071A004 |
0.399 |
|
1993 |
Hanessian S, Couture CA, Georgopapadakou N. Probing the binding site of the penicillin side-chain based on the tipper-strominger hypothesis Bioorganic & Medicinal Chemistry Letters. 3: 2323-2328. DOI: 10.1016/S0960-894X(01)80948-3 |
0.309 |
|
1993 |
Hanessian S, Fu J, Chiara JL, Fabio RD. Total synthesis of (+)-polyoximic acid - cis-3-ethylidene-L-azetidine-2-carboxylic acid Tetrahedron Letters. 34: 4157-4160. DOI: 10.1016/S0040-4039(00)60516-6 |
0.365 |
|
1993 |
Hanessian S, Fu J, Tu Y, Isono K. Structural identity and stereochemical revision of polyoximic acid Tetrahedron Letters. 34: 4153-4156. DOI: 10.1016/S0040-4039(00)60515-4 |
0.32 |
|
1993 |
Hanessian S, Chemla P, Tu Y. Bis-homo avermectin B1a - A semi-synthetic analog with a trienic 18-membered macrocyclic ring Tetrahedron Letters. 34: 1407-1410. DOI: 10.1016/S0040-4039(00)60303-9 |
0.354 |
|
1993 |
Hanessian S, Beaudoin S. Versatile synthesis of alicyclic and acyclic compounds with alternate and remote C-methyl substitution patterns via asymmetric sequential olefination and ene reactions Tetrahedron Letters. 33: 7659-7662. DOI: 10.1016/0040-4039(93)88009-8 |
0.391 |
|
1993 |
Hanessian S, Beaudoin S. Studies in asymmetric olefinations - the synthesis of enantiomerically pure allylidene, alkylidene, and benzylidene cyclohexanes Tetrahedron Letters. 33: 7655-7658. DOI: 10.1016/0040-4039(93)88008-7 |
0.325 |
|
1992 |
Simard M, Beaudoin S, Hanessian S. Structure of a chiral bicyclic β‐hydroxyphosphonamide ‐ a product of kinetic resolution in an olefination reaction, C22H35N2O2P Acta Crystallographica Section C. 48: 1535-1537. DOI: 10.1107/S0108270191014695 |
0.319 |
|
1992 |
Belanger-Gariepy F, Leger R, Hanessian S. Structure of a bicyclic organostannane resulting from a trimethyltin hydride addition-cyclization reaction Acta Crystallographica Section C-Crystal Structure Communications. 48: 1309-1310. DOI: 10.1107/S0108270191013793 |
0.319 |
|
1992 |
Hanessian S, Léger R. Total Synthesis of the Lignan Antibiotic Burseran and a Novel Approach to the Podophyllotoxin Skeleton Synlett. 1992: 402-404. DOI: 10.1055/S-1992-21359 |
0.36 |
|
1992 |
Hanessian S, Sumi K, Vanasse B. The Stereocontrolled Synthesis of (2S,3R)-3-Alkyl-L-aspartic Acids Using a 2-Azetidinone Framework as a Chiral Template Synlett. 1992: 33-34. DOI: 10.1055/S-1992-21255 |
0.347 |
|
1992 |
Hanessian S, Girard C, Chiara JL. A practical synthesis of 2-deoxy aldonolactones via a SmI2-mediated α-deoxygenation reaction Tetrahedron Letters. 33: 573-576. DOI: 10.1016/S0040-4039(00)92313-X |
0.33 |
|
1992 |
Sumi K, Fabio RD, Hanessian S. The stereocontrolled synthesis of versatile carbapenem intermediates using the Barton O-acyl 2-thiophyridylhydroxamate fragmentation Tetrahedron Letters. 33: 749-752. DOI: 10.1016/S0040-4039(00)77706-9 |
0.365 |
|
1992 |
Boulanger Y, Tu Y, Ratovelomanana V, Purisima E, Hanessian S. Conformation of MurNAc-L-Ala-D-iGln (MDP) and of a constrained analog using 1H NMR data and molecular modeling Tetrahedron. 48: 8855-8868. DOI: 10.1016/S0040-4020(01)81985-2 |
0.312 |
|
1992 |
Hanessian S, Léger R, Alpegiani M. Free radical-induced C-allylation of α-bromolactones. Synthesis of 2-C-allyl-2-deoxy-d-arabino-and -d-ribono-1,4-lactones Carbohydrate Research. 228: 145-155. DOI: 10.1016/S0008-6215(00)90556-1 |
0.328 |
|
1991 |
Hanessian S, Sumi K. On the stereochemical divergence in the conjugate addition of lithium dimethylcuprate/trimethylsilyl chloride to γ-alkoxy and γ-ureido α,β-unsaturated esters Synthesis. 1991: 1083-1089. DOI: 10.1055/S-1991-28396 |
0.311 |
|
1991 |
Hanessian S, Ratovelomanana V. Synthesis of a Conformationally Constrained Analog ofN-Acetylmuramyl Dipeptide (MDP) Synlett. 1991: 222-224. DOI: 10.1055/S-1991-20684 |
0.431 |
|
1991 |
Hanessian S, Faucher AM. General stereocontrolled strategy for the heteroyohimbine alkaloids: the total synthesis of (-)-ajmalicine and (+)-19-epiajmalicine The Journal of Organic Chemistry. 56: 2947-2949. DOI: 10.1021/Jo00009A001 |
0.35 |
|
1991 |
Chiara JL, Cabri W, Hanessian S. The stereocontrolled formation of cyclic vicinal cis-diols via a samarium diiodide pinacol coupling of dialdehydes Tetrahedron Letters. 32: 1125-1128. DOI: 10.1016/S0040-4039(00)92024-0 |
0.599 |
|
1991 |
Hanessian S, Chemla P. Synthesis of 19-epi-avermectin A1a from avermectin B1a Tetrahedron Letters. 32: 2719-2722. DOI: 10.1016/0040-4039(91)85067-F |
0.318 |
|
1990 |
Hanessian S, Franco J, Larouche B. The psychobiological basis of heuristic synthesis planning - man, machine and the chiron approach Pure and Applied Chemistry. 62: 1887-1910. DOI: 10.1351/Pac199062101887 |
0.364 |
|
1990 |
Hanessian S, Bennani YL, Fabio RD. Intramolecular free-radical ring closures. III, Structure of a chiral δ-lactone Acta Crystallographica Section C-Crystal Structure Communications. 46: 939-941. DOI: 10.1107/S0108270189010796 |
0.339 |
|
1990 |
Hanessian S, Bennani YL, Fabio RD. Intramolecular free-radical ring closures. I, structure of a chiral bicyclic lactone Acta Crystallographica Section C-Crystal Structure Communications. 46: 934-936. DOI: 10.1107/S0108270189010772 |
0.344 |
|
1990 |
Hanessian S, Roy PJ, Petrini M, Hodges PJ, Fabio RD, Carganico G. Synthetic Studies on the Mevinic Acids Using the Chiron Approach: Total Synthesis of (+)-Dihydromevinolin." Journal of Organic Chemistry. 55: 5766-5777. DOI: 10.1021/Jo00309A022 |
0.392 |
|
1990 |
Hanessian S, Fabio RD, Marcoux JF, Prud'homme M. The synthesis of substituted lactones by intramolecular chirality transfer with stereodifferentiating chiral .alpha.-ester radical intermediates Journal of Organic Chemistry. 55: 3436-3438. DOI: 10.1021/Jo00298A005 |
0.375 |
|
1990 |
Hanessian S, Desilets D, Bennani YL. A novel ring-closure strategy for the carbapenems: the total synthesis of (+)-thienamycin The Journal of Organic Chemistry. 55: 3098-3103. DOI: 10.1021/Jo00297A026 |
0.384 |
|
1990 |
Hanessian S, Cooke NG, DeHoff B, Sakito Y. The total synthesis of (+)-ionomycin Journal of the American Chemical Society. 112: 5276-5290. DOI: 10.1021/Ja00169A041 |
0.409 |
|
1990 |
Hanessian S, Bennani YL. A versatile asymmetric synthesis of α-amino α-alkyl-phosphonic acids of high enantiomeric purity Tetrahedron Letters. 31: 6465-6468. DOI: 10.1016/S0040-4039(00)97092-8 |
0.361 |
|
1990 |
Hanessian S, Bennani YL, Delorme D. The asymmetric synthesis of α-chloro α-alkyl and α-methyl α-alkyl phosphonic acids of high enantiomeric purity. Tetrahedron Letters. 31: 6461-6464. DOI: 10.1016/S0040-4039(00)97091-6 |
0.328 |
|
1990 |
Hanessian S, Faucher A, Léger S. Total synthesis of (+)-meroquinene Tetrahedron. 46: 231-243. DOI: 10.1016/S0040-4020(01)97595-7 |
0.378 |
|
1989 |
Belanger-Gariepy F, Bennani YL, Hanessian S, Brisse F. Structure of a chiral chloropropyl bicyclic phosphonamide Acta Crystallographica Section C-Crystal Structure Communications. 45: 289-291. DOI: 10.1107/S0108270188011138 |
0.311 |
|
1989 |
Belanger-Gariepy F, Roy P, Hanessian S, Brisse F. Structure of a tricyclic lactone – an important intermediate for the total synthesis of dihydromevinolin Acta Crystallographica Section C-Crystal Structure Communications. 45: 145-148. DOI: 10.1107/S0108270188010285 |
0.406 |
|
1989 |
Hanessian S, Sakito Y, Dhanoa D, Baptistella L. Synthesis of (+)-palitantin Tetrahedron. 45: 6623-6630. DOI: 10.1016/S0040-4020(01)89132-8 |
0.398 |
|
1989 |
Hanessian S, Alpegiani M. Highly stereoselective free radical C-6-allylation of penams - synthesis of a noval β-lactamase inhibitor Tetrahedron. 45: 941-950. DOI: 10.1016/0040-4020(89)80006-7 |
0.319 |
|
1987 |
Hanessian S, Ugolini A, Hodges PJ, Beaulieu P, Dube D, Andre C. Progress in natural product chemistry by the chiron and related approaches - synthesis of avermectin B1a Pure and Applied Chemistry. 59: 299-316. DOI: 10.1351/Pac198759030299 |
0.335 |
|
1987 |
Hanessian S, Dhanoa DS, Beaulieu PL. Synthesis of carbocycles from ω-substituted α,β-unsaturated esters via radical-induced cyclizations Canadian Journal of Chemistry. 65: 1859-1866. DOI: 10.1139/V87-312 |
0.394 |
|
1987 |
Hanessian S, Vanasse B. A synthetic strategy for tricholomic acid and acivicin Canadian Journal of Chemistry. 65: 195-199. DOI: 10.1139/V87-031 |
0.336 |
|
1987 |
Desilets D, Belanger-Gariepy F, Hanessian S, Brisse F. Structure and stereochemistry of a carbapenam derivative Acta Crystallographica Section C-Crystal Structure Communications. 43: 919-922. DOI: 10.1107/S0108270187093570 |
0.319 |
|
1987 |
Hanessian S, Kagotani M. A Novel Regiospecific Synthesis of 2-Substituted Pyridines Synthesis. 1987: 409-411. DOI: 10.1055/S-1987-27967 |
0.369 |
|
1987 |
Hanessian S, Botta M. Methodology for the polyene and related antibiotics-versatile and practical access to bifunctional all-trans polyolefinic systems Tetrahedron Letters. 28: 1151-1154. DOI: 10.1016/S0040-4039(00)95312-7 |
0.322 |
|
1987 |
Hanessian S, Sahoo SP, Botta M. Methodology fro the polyene and related antibiotics--enantiospecific synthesis of chiral structural units of amphotericin B from A common progenior: the C1–C13 polyol segment Tetrahedron Letters. 28: 1143-1146. DOI: 10.1016/S0040-4039(00)95310-3 |
0.375 |
|
1987 |
Hanessian S, Murray P. Stereochemical control of nature's biosynthetic pathways:A general strategy for the synthesis 0f polypropionate-derived structural units from a single chiral progenitor Tetrahedron. 43: 5055-5072. DOI: 10.1016/S0040-4020(01)87683-3 |
0.409 |
|
1986 |
Hanessian S, Murray PJ. A highly convergent and enantiospecific synthesis of acyclic subunits of ionomycin from a single chiral progenitor Canadian Journal of Chemistry. 64: 2232-2234. DOI: 10.1139/V86-368 |
0.377 |
|
1986 |
Bedeschi A, Bélanger-Gariépy F, Hanessian S, Brisse F. Structure and absolute configuration of a penam derivative Acta Crystallographica Section C-Crystal Structure Communications. 42: 442-445. DOI: 10.1107/S0108270186095859 |
0.35 |
|
1986 |
Belanger-Gariepy F, Delorme D, Hanessian S, Brisse F. The structures of two chiral bicyclic phosphonamides Acta Crystallographica Section C-Crystal Structure Communications. 42: 856-860. DOI: 10.1107/S0108270186094295 |
0.319 |
|
1986 |
Hanessian S, Hodges PJ, Murray PJ, Sahoo SP. Mild and efficient preparation of γ-substituted α,β-unsturated γ-butyrolactones from epoxides Journal of the Chemical Society, Chemical Communications. 754-755. DOI: 10.1039/C39860000754 |
0.313 |
|
1986 |
Hanessian S, Beaulieu P, Dubé D. A novel synthetic route to the hexahydrobenzofuran subunit of the avermectins and milbemycins Tetrahedron Letters. 27: 5071-5074. DOI: 10.1016/S0040-4039(00)85135-7 |
0.357 |
|
1986 |
Hanessian S, Hodges PJ, Sahoo SP, Roy PJ. The Use of 3‐Phenylselenobutanal as a Crotonaldehyde Equivalent in Synthesis. Tetrahedron Letters. 27: 2949-2952. DOI: 10.1016/S0040-4039(00)84687-0 |
0.31 |
|
1986 |
Hanessian S, Ugolini A, Dube D, Hodges PJ, Andre C. Synthesis of (+)-avermectin B1a Journal of the American Chemical Society. 108: 2776-2778. DOI: 10.1002/Chin.198637328 |
0.408 |
|
1986 |
Hanessian S, Kloss J, Sugawara T. Stereocontrolled access to the octosyl acids - total synthesis of octosyl acid A Journal of the American Chemical Society. 108: 2758-2759. DOI: 10.1002/Chin.198637321 |
0.326 |
|
1986 |
Hanessian S, Guindon Y, Lavallee P, Dextraze P. Total Synthesis of 11‐Oxaprostaglandin F2α and F2β. Cheminform. 17. DOI: 10.1002/Chin.198606321 |
0.649 |
|
1985 |
Hanessian S, Couture C, Wyss H. Design and reactivity of organic functional groups—utility of imidazolylsulfonates in the synthesis of monobactams and 3-amino nocardicinic acid Canadian Journal of Chemistry. 63: 3613-3617. DOI: 10.1139/V85-593 |
0.387 |
|
1985 |
Hanessian S, Roy R. Chemistry of spectinomycin: its total synthesis, stereocontrolled rearrangement, and analogs Canadian Journal of Chemistry. 63: 163-172. DOI: 10.1139/V85-026 |
0.433 |
|
1985 |
Hanessian S, Sahoo SP, Murray PJ. A tactically novel alternative to acyclic stereoselection based on the concept of a replicating chiron — access to 1,3-polyols Tetrahedron Letters. 26: 5631-5634. DOI: 10.1016/S0040-4039(01)80905-9 |
0.337 |
|
1985 |
Hanessian S, Murray PJ, Sahoo SP. A tactically novel alternative to acyclic stereoselection based on the concept of a replicating chiron - 1,5-C-methyl substitution Tetrahedron Letters. 26: 5623-5626. DOI: 10.1016/S0040-4039(01)80903-5 |
0.33 |
|
1985 |
Hanessian S, Kloss J. Total synthesis of biologically important amino sugars via thenitroaldol reaction Tetrahedron Letters. 26: 1261-1264. DOI: 10.1016/S0040-4039(00)94865-2 |
0.343 |
|
1985 |
Hanessian S, Guindon Y, Lavallée P, Dextraze P. Total synthesis of 11-oxaprostaglandin F2α and F2β Carbohydrate Research. 141: 221-238. DOI: 10.1016/S0008-6215(00)90454-3 |
0.646 |
|
1985 |
Hanessian S, Bedeschi A, Battistini C, Mongelli N. Novel synthetic approaches to the penems: total synthesis of Penem FCE 22101 Cheminform. 17: 43-49. DOI: 10.1002/Chin.198619358 |
0.362 |
|
1985 |
Hanessian S, Hoornaert C, Pernet AG, Nadzan AM. Design and synthesis of potential megacaloric parenteral nutrients Carbohydrate Research. 137: C14-C16. DOI: 10.1002/Chin.198535317 |
0.321 |
|
1984 |
Hanessian S, Ugolini A, Dubé D, Glamyan A. Facile access to (S)-1,2,4-butanetriol and its derivatives Canadian Journal of Chemistry. 62: 2146-2147. DOI: 10.1139/V84-367 |
0.348 |
|
1984 |
Hanessian S, Sahoo SP. Synthetic approaches to β-lactam antibiotics: a stereocontrolled synthesis of trans 3-(S)-amino-4-(S)-ethyl-2-oxo-1-azetidine Canadian Journal of Chemistry. 62: 1400-1402. DOI: 10.1139/V84-237 |
0.406 |
|
1984 |
Hanessian S, Delorme D, Beaudoin S, LeBlanc Y. Additions and Corrections - Design and Reactivity of Topologically Unique, Chiral Phosphonamides. Remarkable Diastereofacial Selectivity in Asymmetric Olefination and Alkylation. Journal of the American Chemical Society. 106: 8330-8330. DOI: 10.1021/Ja00338A602 |
0.321 |
|
1984 |
Hanessian S, Delorme D, Beaudoin S, Leblanc Y. Design and reactivity of topologically unique, chiral phosphonamides. Remarkable diastereofacial selectivity in asymmetric olefination and alkylation Journal of the American Chemical Society. 106: 5754-5756. DOI: 10.1021/Ja00331A070 |
0.318 |
|
1984 |
Hanessian S, Delorme D, Dufresne Y. Mild cleavage of methoxymethyl (MOM) ethers with trimethylsilyl bromide Tetrahedron Letters. 25: 2515-2518. DOI: 10.1016/S0040-4039(01)81219-3 |
0.328 |
|
1984 |
Hanessian S, Sahoo SP. A novel and efficient synthesis of L-vinylglycine Tetrahedron Letters. 25: 1425-1428. DOI: 10.1016/S0040-4039(01)80177-5 |
0.366 |
|
1984 |
Hanessian S, Ugolini A. Synthesis of a chiral 1,7-dioxaspiro[5,5]undecene. A model for the spiroacetal subunit of avermectin B1a Carbohydrate Research. 130: 261-269. DOI: 10.1002/Chin.198449312 |
0.357 |
|
1983 |
Hanessian S, Delorme D, Tyler PC, Demailly G, Chapleur Y. Total synthesis of the C-3 – C-17 segment of boromycin Canadian Journal of Chemistry. 61: 634-637. DOI: 10.1139/V83-115 |
0.324 |
|
1983 |
Hanessian S, Ugolini A, Therien M. Stereocontrolled synthesis of the spiro ketal unit of avermectin B1a aglycon Journal of Organic Chemistry. 48: 4427-4430. DOI: 10.1021/Jo00171A065 |
0.39 |
|
1983 |
HANESSIAN S, DELORME D, TYLER PC, DEMAILLY G, CHAPLEUR Y. ChemInform Abstract: Carbohydrates as "Chiral Templates" in Organic Synthesis - Target: Boromycin (33 Literaturzitate). Chemischer Informationsdienst. 14. DOI: 10.1002/Chin.198343363 |
0.341 |
|
1983 |
Hanessian S, Desilets D, Rancourt G, Fortin R. The Total, Stereocontrolled Synthesis Of A Chemical Precursor To (+)-Thienamycin. A Formal Synthesis Of The Antibiotic Cheminform. 14. DOI: 10.1002/Chin.198302352 |
0.415 |
|
1982 |
Hanessian S, Desilets D, Rancourt G, Fortin R. The total, stereocontrolled synthesis of a chemical precursor to (+)-thienamycin. A formal synthesis of the antibiotic Canadian Journal of Chemistry. 60: 2292-2294. DOI: 10.1139/V82-327 |
0.426 |
|
1982 |
Hanessian S, Pougny JR, Boessenkool IK. Total synthesis of the C19-C29 aliphatic segment of (+)-rifamycin S - A formal synthesis of the antibiotic Journal of the American Chemical Society. 104: 6164-6166. DOI: 10.1021/Ja00386A076 |
0.349 |
|
1982 |
Hanessian S, Leblanc Y, Lavallée P. Design and reactivity of organic functional groups: the highly crystalline 2-alkoxy N,N′-diphenyl-1,3,2-diazaphospholanes and their facile conversion into alkyl halides Tetrahedron Letters. 23: 4411-4414. DOI: 10.1016/S0040-4039(00)85615-4 |
0.345 |
|
1982 |
Hanessian S, Demailly G, Chapleur Y, Leger S. Facile Access To Chiral 5-Hydroxy-2-Methylhexanoic Acid Lactones (Pheromones Of The Carpenter Bee) Cheminform. 13. DOI: 10.1002/Chin.198212251 |
0.332 |
|
1982 |
HANESSIAN S, TYLER PC, DEMAILLY G, CHAPLEUR Y. ChemInform Abstract: TOTAL SYNTHESIS AND STEREOCHEMICAL IDENTITY OF THE C18H32O5 DEGRADATION PRODUCT FROM BOROMYCIN Chemischer Informationsdienst. 13. DOI: 10.1002/Chin.198203309 |
0.364 |
|
1981 |
Hanessian S, Roy R, Therien M, Delorme D. Synthesis of 4-amino-4-(S)-dihydrospectinomycin Journal of Antibiotics. 34: 350-352. PMID 6456250 DOI: 10.7164/Antibiotics.34.350 |
0.359 |
|
1981 |
Hanessian S, Dixit DM, Liak TJ. Studies directed toward the total synthesis of the ezomycins, the octosyl acids and related antibiotics Pure and Applied Chemistry. 53: 129-148. DOI: 10.1351/Pac198153010129 |
0.368 |
|
1981 |
Hanessian S, Demailly G, Chapleur Y, Leger S. Facile access to chiral 5-hydroxy-2-methylhexanoic acid lactones (pheromones of the carpenter Bee) Journal of the Chemical Society, Chemical Communications. 1125-1126. DOI: 10.1039/C39810001125 |
0.363 |
|
1981 |
Hanessian S, Tyler PC, Demailly G, Chapleur Y. Total synthesis and stereochemical identity of the C18H32O5 degradation product from boromycin Journal of the American Chemical Society. 103: 6243-6246. DOI: 10.1021/Ja00410A056 |
0.356 |
|
1981 |
Hanessian S, Tyler PC, Chapleur Y. Reaction of lithium dimethylcuprate with conformationally biased β-acyloxy enol esters - regio and stereocontrolled access to functionalized six-carbon chiral synthons Tetrahedron Letters. 22: 4583-4586. DOI: 10.1016/S0040-4039(01)82987-7 |
0.365 |
|
1981 |
Hanessian S, Roy R. A stereocontrolled rearrangement of spectinomycin - the stereochemical identity of spectinoic acid Tetrahedron Letters. 22: 1005-1008. DOI: 10.1016/S0040-4039(01)82851-3 |
0.338 |
|
1981 |
Hanessian S, Jiam Liak T, Dixit DM. Synthesis of trans-fused perhydrofuropyrans and related α-methylene lactones: bicyclic ring-systems present in the ezomycins, the octosyl acids, and certain antitumor terpenoids Carbohydrate Research. 88: C14-C19. DOI: 10.1016/S0008-6215(00)84618-2 |
0.373 |
|
1981 |
Hanessian S, Lavallee P. Total synthesis of (+)-thromboxane B2 from D-glucose. A detailed account Canadian Journal of Chemistry. 59: 870-877. DOI: 10.1002/Chin.198130350 |
0.32 |
|
1980 |
Steliou K, Szczygielska-Nowosielska A, Favre A, Poupart MA, Hanessian S. Reagents for organic synthesis: use of organostannyl oxides as catalytic neutral esterification agents in the preparation of macrolides Journal of the American Chemical Society. 102: 7578-7579. DOI: 10.1021/Ja00545A038 |
0.31 |
|
1980 |
Hanessian S, Guindon Y. Cleavage of methyl and benzyl ethers with thiotrimethylsilanes Tetrahedron Letters. 21: 2305-2308. DOI: 10.1016/S0040-4039(00)92591-7 |
0.591 |
|
1980 |
Hanessian S, Guindon Y. Chemistry of the glycosidic linkage. Direct conversion of glycosides into 1-thioglycosides by use of [alkyl(or aryl)thio]trimethylsilanes Carbohydrate Research. 86: C3-C6. DOI: 10.1016/S0008-6215(00)85913-3 |
0.603 |
|
1979 |
Hanessian S, Roy R. Synthesis of (+)-spectinomycin Journal of the American Chemical Society. 101: 5839-5841. DOI: 10.1021/Ja00513A070 |
0.414 |
|
1979 |
Hanessian S. Approaches to the total synthesis of natural products using "chiral templates" derived from carbohydrates Accounts of Chemical Research. 10: 159-165. DOI: 10.1021/Ar50137A001 |
0.382 |
|
1979 |
Hanessian S, Frenette R. Total stereospecific synthesis of (+) azimic and (+) carpamic acids from D-glucose Tetrahedron Letters. 20: 3391-3394. DOI: 10.1016/S0040-4039(01)95417-6 |
0.337 |
|
1978 |
Hanessian S, Massé R, Capmeau ML. Aminoglycoside antibiotics: synthesis of 5''-amino-5''-deoxyneomycin and 5''-amino-5''-deoxyparomomycin. The Journal of Antibiotics. 30: 893-6. PMID 591451 DOI: 10.7164/Antibiotics.30.893 |
0.363 |
|
1978 |
Hanessian S, Rancourt G, Guindon Y. Assembly of the carbon skeletal framework of erythronolide A Canadian Journal of Chemistry. 56: 1843-1846. DOI: 10.1139/V78-299 |
0.586 |
|
1978 |
Hanessian S, Massé R, Nakagawa T. Aminoglycoside antibiotics: Studies directed toward the selective modification of hydroxyl groups: Synthesis of 3′-epiparomamine and 3′-epineamine Canadian Journal of Chemistry. 56: 1509-1517. DOI: 10.1139/V78-245 |
0.388 |
|
1978 |
Hanessian S, Massé R, Ekborg G. Aminoglycoside antibiotics: The formation and characterization of dihydrooxazine derivatives in the paromomycin series Canadian Journal of Chemistry. 56: 1492-1499. DOI: 10.1139/V78-243 |
0.345 |
|
1978 |
Hanessian S, Bargiotti A, LaRue M. A mild and stereospecific conversion of vicinal diols into olefins Tetrahedron Letters. 19: 737-740. DOI: 10.1016/S0040-4039(01)85381-8 |
0.321 |
|
1978 |
Hanessian S, Masse R, Ekborg G. Aminoglycoside Antibiotics‐ The Formation And Characterization Of Dihydrooxazine Derivatives In The Paromomycin Series Cheminform. 9. DOI: 10.1002/Chin.197840333 |
0.309 |
|
1978 |
Hanessian S, Takamoto T, Massé R, Patil G. Aminoglycoside antibiotics: Chemical conversion of neomycin B, paromomycin, and lividomycin B into bioactive pseudosaccharides Canadian Journal of Chemistry. 56: 1482-1491. DOI: 10.1002/Chin.197840332 |
0.305 |
|
1978 |
Hanessian S, Masse R, Nakagawa T. Aminoglycoside Antibiotics: Studies Directed Toward The Selective Modification Of Hydroxyl Groups: Synthesis Of 3′‐Epiparomamine And 3′‐Epineamine Cheminform. 9. DOI: 10.1002/Chin.197840322 |
0.366 |
|
1978 |
Hanessian S, Ogawa T, Takamoto T. Aminoglycoside antibiotics: Synthesis of pseudotrisaccharides derived from neamine and paromamine Canadian Journal of Chemistry. 56: 1500-1508. DOI: 10.1002/Chin.197840321 |
0.345 |
|
1977 |
Arcamone F, Penco S, Redaelli S, Hanessian S. Synthesis and antitumor activity of 4'-deoxydaunorubicin and 4'-deoxyadriamycin. Journal of Medicinal Chemistry. 19: 1424-5. PMID 1003430 DOI: 10.1021/Jm00234A016 |
0.372 |
|
1977 |
Bargiotti A, Cassinelli G, Franchi G, Gioia B, Lazzari E, Redaelli S, Vigevani A, Arcamone F, Hanessian S. Synthesis of derivatives of 3-amino-2,3-dideoxy-l-hexoses related to daunosamine (3-amino-2,3,6-trideoxy-l-lyxo-hexose) Carbohydrate Research. 58: 353-361. PMID 912692 DOI: 10.1016/S0008-6215(00)84362-1 |
0.314 |
|
1977 |
Hanessian S, Pernet AG. Synthesis of naturally occurring C-nucleosides, their analogs, and functionalized C-glycosyl precursors. Advances in Carbohydrate Chemistry and Biochemistry. 33: 111-88. PMID 793324 DOI: 10.1016/S0065-2318(08)60281-4 |
0.348 |
|
1977 |
Hanessian S, Rancourt G. Approaches to the total synthesis of natural products from carbohydrates Pure and Applied Chemistry. 49: 1201-1214. DOI: 10.1351/Pac197749081201 |
0.387 |
|
1977 |
Hanessian S, Rancourt G. Carbohydrates as chiral intermediates in organic synthesis. Two functionalized chemical precursors comprising eight of the ten chiral centers of erythronolide A Canadian Journal of Chemistry. 55: 1111-1113. DOI: 10.1139/V77-155 |
0.368 |
|
1977 |
Hanessian S, Lavallee P. A stereospecifie, total synthesis of thromboxane B2 Canadian Journal of Chemistry. 55: 562-565. DOI: 10.1139/V77-079 |
0.331 |
|
1977 |
Hanessian S, Banoub J. Chemistry of the glycosidic linkage. An efficient synthesis of 1,2-trans-di-saccharides Carbohydrate Research. 53. DOI: 10.1016/S0008-6215(00)85468-3 |
0.397 |
|
1977 |
Hanessian S, Masse R. Photochemical cleavage of theN-(benzyloxycarbonyl) group in amino sugar derivatives Carbohydrate Research. 54: 142-144. DOI: 10.1016/S0008-6215(00)80563-7 |
0.31 |
|
1977 |
Arcamone F, Penco S, Redaelli S, Hanessian S. Synthesis And Antitumor Activity Of 4′-Deoxydaunorubicin And 4′-Deoxyadriamycin Cheminform. 8. DOI: 10.1002/Chin.197715379 |
0.382 |
|
1976 |
Arcamone F, Bargiotii A, Cassinelli G, Redaelli S, Hanessian S, Di Marco A, Casazza AM, Dasdia T, Necco A, Reggiani P, Supino R. Stereocontrolled glycosidation of daunomycinone. Synthesis and biological evaluation of 6-hydroxy-L-arabino analogues of antitumor anthracyclines. Journal of Medicinal Chemistry. 19: 733-4. PMID 1271420 DOI: 10.1002/Chin.197640373 |
0.354 |
|
1976 |
Arcamone F, Bargiotti A, Cassinelli G, Penco S, Hanessian S. Synthesis of a configurational analog of daunorubicin. Carbohydrate Research. 46: C3-5. PMID 1260787 DOI: 10.1016/S0008-6215(00)84305-0 |
0.422 |
|
1976 |
Hanessian S, Banoub J. Chemistry of the glycosidic linkage. Lewis acid catalyzed glycosidations with amide acetals and lactim ethers. Tetrahedron Letters. 17: 657-660. DOI: 10.1016/S0040-4039(00)74589-8 |
0.347 |
|
1976 |
HANESSIAN S, LAVALLEE P. ChemInform Abstract: PREPARATION AND SYNTHETIC UTILITY OF TERT-BUTYLDIPHENYLSILYL ETHERS Chemischer Informationsdienst. 7: no-no. DOI: 10.1002/Chin.197613286 |
0.367 |
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1975 |
Hanessian S, Lavallee P. The Preparation and Synthetic Utility of tert-Butyldiphenylsilyl Ethers Canadian Journal of Chemistry. 53: 2975-2977. DOI: 10.1139/V75-419 |
0.356 |
|
1975 |
Hanessian S, Cassinelli G, Casey M. Chemistry of the glycosidic linkage. 2-Alkoxy-3-(p-nitrobenzoyl)-2-phenyl-4,5-[α-D-glucopyrano]-2-oxazolidines, a new class of carbohydrate 1,2-ortho-acid derivative Carbohydrate Research. 44: C18-C21. DOI: 10.1016/S0008-6215(00)84181-6 |
0.319 |
|
1975 |
hanessian S, Banoub J. Chemistry of the glycosidic linkage. A rapid and efficient synthesis of carbohydrate 1,2-orthoesters Carbohydrate Research. 44: C14-C17. DOI: 10.1016/S0008-6215(00)84180-4 |
0.378 |
|
1975 |
HANESSIAN S, DEXTRAZE P, FOUGEROUSSE A, GUINDON Y. ChemInform Abstract: STERISCH KONTROLLIERTE SYNTHESE VON CHIRALEN VORLAEUFERN DER 11-OXAPROSTAGLANDINE Chemischer Informationsdienst. 6: no-no. DOI: 10.1002/Chin.197506458 |
0.606 |
|
1974 |
Hanessian S, Masse R. Synthetic approaches to kasugamine. Carbohydrate Research. 35: 175-85. PMID 4854593 DOI: 10.1016/S0008-6215(00)84844-2 |
0.353 |
|
1974 |
Hanessian S, Pernet AG. Carbanions in Carbohydrate Chemistry: Approaches to Chemical Precursors of C-Nucleosides Canadian Journal of Chemistry. 52: 1280-1293. DOI: 10.1139/V74-198 |
0.345 |
|
1974 |
Hanessian S, Pernet AG. Carbanions in Carbohydrate Chemistry: Synthesis of C-Glycosyl Malonates Canadian Journal of Chemistry. 52: 1266-1279. DOI: 10.1139/V74-197 |
0.314 |
|
1974 |
Hanessian S, Staub APA. Elimination, Oxidation, and Transposition Reactions in Conformationally Biased Carbohydrates: Methyl 4,6-O-Benzylidene-α-D-Altropyranosides Containing the Phenylthio Group Canadian Journal of Chemistry. 52: 1258-1265. DOI: 10.1139/V74-196 |
0.333 |
|
1974 |
Ogawa T, Takamoto T, Hanessian S. Aminoglycoside antibiotics: synthesis of 6-0-(β-D-ribofuranosyl) paromamine Tetrahedron Letters. 15: 4013-4016. DOI: 10.1016/S0040-4039(01)92071-4 |
0.315 |
|
1974 |
Hanessian S, Dextraze P, Fougerousse A, Guindon Y. Synthese stereocontrolee des precurseurs chiraux des 11-oxaprostaglandines Tetrahedron Letters. 15: 3983-3986. DOI: 10.1016/S0040-4039(01)92063-5 |
0.555 |
|
1974 |
Hanessian S, Ogawa T, Guindon Y, Kamennof JL, Roy R. Utilization of functionalized polymers in synthesis: immobilization of carbohydrates as acetals, and some chemical transformations Carbohydrate Research. 38: C15-C18. DOI: 10.1016/S0008-6215(00)82382-4 |
0.577 |
|
1974 |
Hanessian S, Ogawa T, Guindon Y. Facile access to ethyl 2-C-β-D-ribofuranosylacetates Carbohydrate Research. 38: C12-C14. DOI: 10.1016/S0008-6215(00)82381-2 |
0.562 |
|
1974 |
HANESSIAN S, PERNET AG. ChemInform Abstract: PREPARATIVE AND EXPLORATORY CARBOHYDRATE CHEMISTRY. CARBANIONS IN CARBOHYDRATE CHEMISTRY, APPROACHES TO CHEMICAL PRECURSORS OF C-NUCLEOSIDES Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/Chin.197429424 |
0.316 |
|
1974 |
HANESSIAN S, PERNET AG. ChemInform Abstract: PREPARATIVE AND EXPLORATORY CARBOHYDRATE CHEMISTRY. CARBANIONS IN CARBOHYDRATE CHEMISTRY, SYNTHESIS OF C-GLYCOSYL MALONATES Chemischer Informationsdienst. 5: no-no. DOI: 10.1002/Chin.197429423 |
0.389 |
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1973 |
Hanessian S, Lavallee P. Synthesis of 6-amino-6-deoxy- , -trehalose: a positional isomer of trehalosamine. The Journal of Antibiotics. 25: 683-4. PMID 4647840 DOI: 10.7164/Antibiotics.25.683 |
0.381 |
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1973 |
Hanessian S, Lavallee P, Pernet AG. A new synthesis of methylene acetals Carbohydrate Research. 26: 258-260. DOI: 10.1016/S0008-6215(00)85050-8 |
0.388 |
|
1973 |
Hanessian S, Lavallée P. Selective substitution reactions of α,α-trehalose: preparation of 6-monofunctional derivatives Carbohydrate Research. 28: 303-311. DOI: 10.1016/S0008-6215(00)82785-8 |
0.307 |
|
1972 |
Hanessian S, Ponpipom M, Lavallee P. Procedures for the direct replacement of primary hydroxyl groups in carbohydrates by halogen Carbohydrate Research. 24: 45-56. DOI: 10.1016/S0008-6215(00)82258-2 |
0.329 |
|
1971 |
Butterworth RF, Hanessian S. Methyl 2,3-O-Isopropylidene-β-D-ribo-pentodialdofuranoside: a Useful Intermediate in Chain Extension Reactions Canadian Journal of Chemistry. 49: 2755-2759. DOI: 10.1139/V71-458 |
0.307 |
|
1971 |
Hanessian S, Moralioglu E. Chemistry of 1-(dimethylamino)ethylidene and α-(dimethylamino)benzylidene acetals: utility as blocking group for diols and for selective esterification. Tetrahedron Letters. 12: 813-816. DOI: 10.1016/S0040-4039(01)96563-3 |
0.31 |
|
1971 |
Ponpipom M, Hanessian S. Novel access to 2′-deoxyuridine, and reactive intermediates to pyrimidine nucleosides Carbohydrate Research. 17: 248-251. DOI: 10.1016/S0008-6215(00)81569-4 |
0.358 |
|
1971 |
Hanessian S, Staub APA. Synthesis of carbohydrate derivatives containing vinylic thioether groups1 Carbohydrate Research. 16: 419-433. DOI: 10.1016/S0008-6215(00)81177-5 |
0.328 |
|
1969 |
Hanessian S, Schütze G. Synthetic penicillins derived from cycloheptatrienecarboxylic acids. Journal of Medicinal Chemistry. 12: 527-9. PMID 5788175 DOI: 10.1021/Jm00303A614 |
0.313 |
|
1969 |
Hanessian S, Schütze G. Synthetic penicillins derived from benznorcaradienecarboxylic acids. Journal of Medicinal Chemistry. 12: 529-31. PMID 4892245 DOI: 10.1021/Jm00303A615 |
0.313 |
|
1969 |
Hanessian S, Plessas NR. Reactions of carbohydrates with (halomethylene)dimethyliminium halides and related reagents. Synthesis of some chlorodeoxy sugars Journal of Organic Chemistry. 34: 2163-2170. DOI: 10.1021/Jo01259A030 |
0.35 |
|
1969 |
Hanessian S, Plessas NR. Reaction of O-benzylidene sugars with N-bromosuccinimide. III. Applications to the synthesis of aminodeoxy and deoxy sugars of biological importance The Journal of Organic Chemistry. 34: 1045-1053. DOI: 10.1021/Jo01256A060 |
0.312 |
|
1969 |
Hanessian S. Sugar lactams. III. Synthesis of five-,six-, and seven-membered analogs Journal of Organic Chemistry. 34: 675-681. DOI: 10.1021/Jo01255A042 |
0.395 |
|
1967 |
Hanessian S. Neighboring-group participation across a furanose ring. Synthesis of 5-acetamido-5-deoxy-D-lyxopyranose from D-arabinose precursors The Journal of Organic Chemistry. 32: 163-168. DOI: 10.1021/Jo01277A040 |
0.315 |
|
1966 |
Hanessian S, Kaltenbronn JS. Synthesis of a Bromine-Rich Marine Antibiotic Journal of the American Chemical Society. 88: 4509-4510. DOI: 10.1021/Ja00971A039 |
0.391 |
|
1965 |
Hanessian S, Haskell TH. Synthesis and Characterization of 3,6-Diamino-3,6-dideoxy-D-idose1 The Journal of Organic Chemistry. 30: 1080-1085. DOI: 10.1021/Jo01015A030 |
0.332 |
|
1963 |
Hanessian S, Haskell TH. Synthesis of 5-Acetamido-5-deoxypentoses. Sugar Derivatives Containing Nitrogen in the Ring1 The Journal of Organic Chemistry. 28: 2604-2610. DOI: 10.1021/Jo01045A029 |
0.402 |
|
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