Year |
Citation |
Score |
2024 |
Al Hoque A, Kannaboina P, Abraham Y, Mehedi M, Sibi MP, Quadir M. Furan-rich, biobased transfection agents as potential oligomeric candidates for intracellular plasmid DNA delivery. Rsc Advances. 14: 32637-32647. PMID 39411251 DOI: 10.1039/d4ra05978f |
0.75 |
|
2024 |
So RC, Subramanian H, Kuehn CR, Sibi MP. Relay PHOS: Ligands with Fluxional Chirality in Asymmetric Palladium-Catalyzed Allylic Alkylation. Organic Letters. PMID 39158060 DOI: 10.1021/acs.orglett.4c02629 |
0.313 |
|
2024 |
Shafranska O, Sutton C, Kalita D, Kannaboina P, Tiwari S, Sibi MP, Webster DC. A Preliminary Study of Thermosets from Epoxy Resins Made using Low-Toxicity Furan-Based Diols. Macromolecular Rapid Communications. e2300665. PMID 38444218 DOI: 10.1002/marc.202300665 |
0.747 |
|
2022 |
Mondal S, Dumur F, Gigmes D, Sibi MP, Bertrand MP, Nechab M. Enantioselective Radical Reactions Using Chiral Catalysts. Chemical Reviews. PMID 35073048 DOI: 10.1021/acs.chemrev.1c00582 |
0.301 |
|
2019 |
Nad S, Sibi MP. Asymmetric Synthesis of 2,3‐Disubstituted Cyclic Ketones by Enantioselective Conjugate Radical Additions Helvetica Chimica Acta. 102. DOI: 10.1002/hlca.201900223 |
0.391 |
|
2017 |
Zhao C, Sibi M. Enantioselective and Diastereoselective Conjugate Radical Additions to α-Arylidene Ketones and Lactones Synlett. 28: 2971-2975. DOI: 10.1055/s-0036-1590930 |
0.406 |
|
2017 |
Miah MAJ, Sibi MP, Chattopadhyay S, Familoni OB, Snieckus V. Directed ortho
-Metalation of Aryl Amides, O-
Carbamates, and Methoxymethoxy Systems: Directed Metalation Group Competition and Cooperation European Journal of Organic Chemistry. 2018: 447-454. DOI: 10.1002/Ejoc.201701143 |
0.312 |
|
2016 |
Vallavoju N, Selvakumar S, Pemberton BC, Jockusch S, Sibi MP, Sivaguru J. Organophotocatalysis: Insights into the Mechanistic Aspects of Thiourea-Mediated Intermolecular [2+2] Photocycloadditions. Angewandte Chemie (International Ed. in English). PMID 27005562 DOI: 10.1002/Anie.201600596 |
0.75 |
|
2015 |
Ma G, Sibi MP. Catalytic Kinetic Resolution of Biaryl Compounds. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 11644-57. PMID 26237330 DOI: 10.1002/Chem.201500869 |
0.356 |
|
2015 |
Zhang M, Selvakumar S, Zhang X, Sibi MP, Weiss RG. Structural and solubility parameter correlations of gelation abilities for dihydroxylated derivatives of long-chain, naturally occurring fatty acids. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 8530-43. PMID 25926104 DOI: 10.1002/chem.201500096 |
0.753 |
|
2014 |
Adachi S, Takeda N, Sibi MP. Evaluation of achiral templates with fluxional Brønsted basic substituents in enantioselective conjugate additions. Organic Letters. 16: 6440-3. PMID 25490703 DOI: 10.1021/ol503275w |
0.315 |
|
2014 |
Subramanian H, Moorthy R, Sibi MP. Thiyl radicals: from simple radical additions to asymmetric catalysis. Angewandte Chemie (International Ed. in English). 53: 13660-2. PMID 25339618 DOI: 10.1002/Anie.201408781 |
0.379 |
|
2014 |
Kovash CS, Pavlacky E, Selvakumar S, Sibi MP, Webster DC. Thermoset coatings from epoxidized sucrose soyate and blocked, bio-based dicarboxylic acids Chemsuschem. 7: 2289-2294. PMID 24777954 DOI: 10.1002/Cssc.201402091 |
0.746 |
|
2014 |
Vallavoju N, Selvakumar S, Jockusch S, Sibi MP, Sivaguru J. Enantioselective organo-photocatalysis mediated by atropisomeric thiourea derivatives. Angewandte Chemie (International Ed. in English). 53: 5604-8. PMID 24740511 DOI: 10.1002/Anie.201310940 |
0.772 |
|
2011 |
Stanley LM, Sibi MP. Chiral Bisoxazoline Ligands Privileged Chiral Ligands and Catalysts. 171-219. DOI: 10.1002/9783527635207.ch5 |
0.602 |
|
2010 |
Sibi MP, Gustafson B, Coulomb J. 3-Isoxazolidinone: A new achiral template for enantioselective transformations Bulletin of the Korean Chemical Society. 31: 541-542. DOI: 10.5012/Bkcs.2010.31.03.541 |
0.377 |
|
2010 |
Sibi MP, Cruzjr W, Stanley LM. Enantioselective diels-alder cycloadditions with -substituted pyrazolidinone propiolimides Synlett. 889-892. DOI: 10.1055/S-0029-1219538 |
0.718 |
|
2010 |
Zimmerman J, Halloway A, Sibi MP. ChemInform Abstract: Free Radical Cyclization Reactions Cheminform. 41: no-no. DOI: 10.1002/chin.201037267 |
0.305 |
|
2010 |
GRIBBLE GW, KEAVY DJ, DAVIS DA, SAULNIER MG, PELCMAN B, BARDEN TC, SIBI MP, OLSON ER, BELBRUNO JJ. ChemInform Abstract: Syntheses and Diels-Alder Cycloaddition Reactions of 4H-Furo(3,4-b) indoles. A Regiospecific Diels-Alder Synthesis of Ellipticine. Cheminform. 24: no-no. DOI: 10.1002/chin.199309241 |
0.471 |
|
2009 |
Sibi MP, Soeta T, Jasperse CP. Nitrile ylides: diastereoselective cycloadditions using chiral oxazolidinones without Lewis acid. Organic Letters. 11: 5366-9. PMID 19877629 DOI: 10.1021/Ol9018584 |
0.396 |
|
2009 |
Sibi MP, Kawashima K, Stanley LM. Diels-Alder cycloaddition strategy for kinetic resolution of chiral pyrazolidinones. Organic Letters. 11: 3894-7. PMID 19650642 DOI: 10.1021/Ol901504P |
0.642 |
|
2009 |
Sibi M, Kawashima K, Stanley L. Kinetic Resolution of Pyrazolidinones by a Cu(II)-Catalyzed Diels-Alder Reaction Synfacts. 2009: 1367-1367. DOI: 10.1055/s-0029-1218314 |
0.596 |
|
2009 |
Sibi M, Coulomb J, Stanley L. Enantioselective Protonation of Friedel-Crafts Intermediates Synfacts. 2009: 0302-0302. DOI: 10.1055/s-0028-1087773 |
0.625 |
|
2009 |
Sibi MP, Kawashima K, Stanley LM. Diels-alder cycloaddition strategy for kinetic resolution of chiral pyrazolidinones Organic Letters. 11: 3894-3897. DOI: 10.1021/ol901504p |
0.625 |
|
2008 |
Sibi MP, Coulomb J, Stanley LM. Enantioselective enolate protonations: Friedel-Crafts reactions with alpha-substituted acrylates. Angewandte Chemie (International Ed. in English). 47: 9913-5. PMID 19016291 DOI: 10.1002/Anie.200804221 |
0.664 |
|
2008 |
Sibi MP, Yang YH, Lee S. Tin-free enantioselective radical reactions using silanes Organic Letters. 10: 5349-5352. PMID 18986157 DOI: 10.1021/Ol802154D |
0.447 |
|
2008 |
Zhang Y, Lukacova V, Bartus V, Nie X, Sun G, Manivannan E, Ghorpade SR, Jin X, Manyem S, Sibi MP, Cook GR, Balaz S. Binding of matrix metalloproteinase inhibitors to extracellular matrix: 3D-QSAR analysis. Chemical Biology & Drug Design. 72: 237-48. PMID 18844670 DOI: 10.1111/J.1747-0285.2008.00710.X |
0.712 |
|
2008 |
Stanley LM, Sibi MP. Enantioselective copper-catalyzed 1,3-dipolar cycloadditions Chemical Reviews. 108: 2887-2902. PMID 18613728 DOI: 10.1021/Cr078371M |
0.664 |
|
2008 |
Sibi MP, Rane D, Stanley LM, Soeta T. Copper(II)-catalyzed exo and enantioselective cycloadditions of azomethine imines. Organic Letters. 10: 2971-4. PMID 18549218 DOI: 10.1021/Ol800904T |
0.805 |
|
2008 |
Sibi MP, Yang YH. Chiral Lewis acid catalyzed enantioselective conjugate radical additions to α,β-unsaturated 2-pyridyl ketones Synlett. 0083-0088. DOI: 10.1055/s-2007-992386 |
0.313 |
|
2008 |
Sibi MP, Nie X, Shackleford JP, Stanley LM, Bouret F. Exo- and enantioselective Diels-Alder reactions: Pyrazolidinone auxiliaries as a means to enhanced exo selectivity Synlett. 2655-2658. DOI: 10.1055/S-0028-1083438 |
0.682 |
|
2008 |
Sibi MP, Rane D, Stanley LM, Soeta T. Copper(II)-catalyzed exo and enantioselective cycloadditions of azomethine imines Organic Letters. 10: 2971-2974. DOI: 10.1021/ol800904t |
0.609 |
|
2008 |
Sibi MP, Coulomb J, Stanley LM. Enantioselective enolate protonations: Friedel-crafts reactions with α-substituted acrylates Angewandte Chemie - International Edition. 47: 9913-9915. DOI: 10.1002/anie.200804221 |
0.652 |
|
2007 |
Sibi MP, Nad S. Enantioselective radical reactions: Stereoselective aldol synthesis from cyclic ketones Angewandte Chemie - International Edition. 46: 9231-9234. PMID 17969220 DOI: 10.1002/Anie.200702976 |
0.487 |
|
2007 |
Sibi MP, Itoh K. Organocatalysis in conjugate amine additions. Synthesis of β-amino acid derivatives Journal of the American Chemical Society. 129: 8064-8065. PMID 17552527 DOI: 10.1021/Ja071739C |
0.409 |
|
2007 |
Sibi MP, Stanley LM, Soeta T. Enantioselective 1,3-dipolar cycloadditions of diazoacetates with electron-deficient olefins Organic Letters. 9: 1553-1556. PMID 17367154 DOI: 10.1021/Ol070364X |
0.646 |
|
2007 |
Sibi MP, Soeta T. Enantioselective conjugate addition of hydrazines to alpha,beta-unsaturated imides. Synthesis of chiral pyrazolidinones. Journal of the American Chemical Society. 129: 4522-3. PMID 17362014 DOI: 10.1021/Ja069312D |
0.468 |
|
2007 |
Sibi MP, Hasegawa M. Organocatalysis in radical chemistry. Enantioselective α-oxyamination of aldehydes Journal of the American Chemical Society. 129: 4124-4125. PMID 17362013 DOI: 10.1021/Ja069245N |
0.459 |
|
2007 |
Sibi MP, Stanley LM, Nie X, Venkatraman L, Liu M, Jasperse CP. The role of achiral pyrazolidinone templates in enantioselective Diels-Alder reactions: Scope, limitations, and conformational insights Journal of the American Chemical Society. 129: 395-405. PMID 17212420 DOI: 10.1021/Ja066425O |
0.701 |
|
2007 |
Manyem S, Sibi MP, Lushington GH, Neuenswander B, Schoenen F, Aubé J. Solution-phase parallel synthesis of a library of Δ2- pyrazolines Journal of Combinatorial Chemistry. 9: 20-28. PMID 17206829 DOI: 10.1021/Cc0601175 |
0.76 |
|
2007 |
Sibi MP, Yu A. Diastereoselective conjugate radical additions to β-pyranones Synlett. 3193-3197. DOI: 10.1055/S-2007-992381 |
0.358 |
|
2007 |
Sibi M, Soeta T. Enantioselective Addition of Simple Hydrazines to Unsaturated Imides Synfacts. 2007: 0724-0724. DOI: 10.1055/s-2007-968673 |
0.342 |
|
2007 |
Sibi MP, Stanley LM, Soeta T. Synthesis of Pyrazolines via Enantioselective 1,3-Dipolar Cycloadditions Synfacts. 2007: 605-605. DOI: 10.1055/S-2007-968558 |
0.413 |
|
2007 |
Sibi M, Chen J, Stanley L. Effect of Achiral Templates in Enantioselective Diels-Alder Reactions Synfacts. 2007: 0401-0401. DOI: 10.1055/s-2007-968383 |
0.649 |
|
2007 |
Sibi MP, Chen J, Stanley L. Enantioselective diels-alder reactions: Effect of the achiral template on reactivity and selectivity Synlett. 298-302. DOI: 10.1055/S-2007-968014 |
0.7 |
|
2007 |
Sibi M, Stanley L, Soeta T. Chiral Dihydropyrazoles via Mg(II)-Catalyzed Nitrile Imine Cycloaddition Synfacts. 2007: 0175-0175. DOI: 10.1055/S-2006-955852 |
0.634 |
|
2007 |
Sibi M, Manyem S, Palencia H. Achiral Additives for Enhancing the Stereoselectivity of Cycloadditions Synfacts. 2007: 0074-0074. DOI: 10.1055/S-2006-955729 |
0.786 |
|
2007 |
Sibi M, Zimmerman J. Enantioselective Radical Additions to Acyloxy Pyrones Synfacts. 2007: 0051-0051. DOI: 10.1055/S-2006-955716 |
0.716 |
|
2006 |
Sibi MP, Manyem S, Palencia H. Fluxional additives: a second generation control in enantioselective catalysis. Journal of the American Chemical Society. 128: 13660-1. PMID 17044673 DOI: 10.1021/Ja064472A |
0.796 |
|
2006 |
Sibi MP, Zimmerman J. Pyrones to pyrans: Enantioselective radical additions to acyloxy pyrones Journal of the American Chemical Society. 128: 13346-13347. PMID 17031933 DOI: 10.1021/Ja0648108 |
0.711 |
|
2006 |
Lee S, Chae JL, Kim S, Subramaniam R, Zimmerman J, Sibi MP. Enantioselective conjugate radical addition to α′-hydroxy enones Organic Letters. 8: 4311-4313. PMID 16956214 DOI: 10.1021/Ol061634Z |
0.684 |
|
2006 |
Sibi MP, He L. Enantioselective Radical Reactions. Formation of Chiral Quaternary Centers. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 2006: 689-692. PMID 16799703 DOI: 10.1055/S-2006-933116 |
0.463 |
|
2006 |
Kim S, Sibi M, Lee S, Lim C, Subramaniam R, Zimmerman J. Enantioselective Conjugate Radical Addition Synfacts. 2006: 1264-1264. DOI: 10.1055/S-2006-949491 |
0.719 |
|
2006 |
Sibi MP, He L. Enantioselective radical reactions: Formation of chiral quaternary centers Synlett. 689-692. DOI: 10.1055/s-2006-933116 |
0.376 |
|
2006 |
Sibi MP, Patil K. Enantioselective radical reactions. Evaluation of nitrogen protecting groups in the synthesis of β2-amino acids Tetrahedron Asymmetry. 17: 516-519. DOI: 10.1016/j.tetasy.2006.01.018 |
0.32 |
|
2006 |
Manyem S, Sibi MP. β-Heteroatom-Substituted Alkanamides Cheminform. 37. DOI: 10.1002/chin.200605262 |
0.738 |
|
2006 |
Sibi MP, Stanley LM, Soeta T. Enantioselective 1,3-dipolar cycloaddition of nitrile imines to α-substituted and α,β-disubstituted α,β-unsaturated carbonyl substrates: A method for synthesizing dihydropyrazoles bearing a chiral quaternary center Advanced Synthesis and Catalysis. 348: 2371-2375. DOI: 10.1002/Adsc.200600307 |
0.615 |
|
2006 |
Zimmerman J, Sibi MP. Enantioselective Radical Reactions Cheminform. 37. DOI: 10.1002/9783527618293.Ch23 |
0.705 |
|
2005 |
Hein JE, Zimmerman J, Sibi MP, Hultin PG. Stereoselective conjugate radical additions: Application of a fluorous oxazolidinone chiral auxiliary for efficient tin removal Organic Letters. 7: 2755-2758. PMID 15957939 DOI: 10.1021/Ol050956K |
0.719 |
|
2005 |
Sibi MP, Tatamidani H, Patil K. Enantioselective rhodium enolate protonations. A new methodology for the synthesis of β2-amino acids Organic Letters. 7: 2571-2573. PMID 15957893 DOI: 10.1021/Ol050630B |
0.444 |
|
2005 |
Sibi MP, Stanley LM, Jasperse CP. An entry to a chiral dihydropyrazole scaffold: enantioselective [3 + 2] cycloaddition of nitrile imines. Journal of the American Chemical Society. 127: 8276-7. PMID 15941248 DOI: 10.1021/Ja051650B |
0.689 |
|
2005 |
Sibi MP, Ma Z, Itoh K, Prabagaran N, Jasperse CP. Enantioselective cycloadditions with alpha,beta-disubstituted acrylimides. Organic Letters. 7: 2349-52. PMID 15932195 DOI: 10.1021/Ol050599D |
0.37 |
|
2005 |
Sibi MP, Ma Z, Jasperse CP. Enantioselective addition of nitrones to activated cyclopropanes Journal of the American Chemical Society. 127: 5764-5765. PMID 15839655 DOI: 10.1021/Ja0421497 |
0.475 |
|
2005 |
Sibi MP, Patil K. Enantioselective H-atom transfer reaction: A strategy to synthesize formaldehyde aldol products Organic Letters. 7: 1453-1456. PMID 15816725 DOI: 10.1021/ol047347h |
0.315 |
|
2005 |
Sibi MP, Petrovic G, Zimmerman J. Enantioselective radical addition/trapping reactions with α,β-disubstituted unsaturated imides. Synthesis of anti-propionate aldols Journal of the American Chemical Society. 127: 2390-2391. PMID 15724983 DOI: 10.1021/Ja043371E |
0.685 |
|
2005 |
Gribble GW, Saulnier MG, Pelkey ET, Kishbaugh TLS, Liu Y, Jiang J, Trujillo HA, Keavy DJ, Davis DA, Conway SC, Switzer FL, Roy S, Silva RA, Obaza-Nutaitis JA, Sibi MP, et al. Novel indole chemistry in the synthesis of heterocycles Current Organic Chemistry. 9: 1493-1519. DOI: 10.2174/138527205774370487 |
0.532 |
|
2005 |
Sibi MP, Guerrero MA. Enantioselective radical methods for lactone synthesis: Use of unprotected haloalcohols as radical precursors Synthesis. 1528-1532. DOI: 10.1055/S-2005-865319 |
0.395 |
|
2005 |
Sibi MP, Stanley LM, Jasperse CP. An entry to a chiral dihydropyrazole scaffold: Enantioselective [3 + 2] cycloaddition of nitrile imines Journal of the American Chemical Society. 127: 8276-8277. DOI: 10.1021/ja051650b |
0.649 |
|
2004 |
Sibi MP, He L. Application of enantioselective radical reactions: Synthesis of (+)-ricciocarpins A and B Organic Letters. 6: 1749-1752. PMID 15151405 DOI: 10.1021/ol0495772 |
0.36 |
|
2004 |
Sibi MP, Itoh K, Jasperse CP. Chiral lewis Acid catalysis in nitrile oxide cycloadditions. Journal of the American Chemical Society. 126: 5366-7. PMID 15113201 DOI: 10.1021/Ja0318636 |
0.383 |
|
2004 |
Sibi MP, Patil K. Enantioselective H-atom transfer reactions: A new methodology for the synthesis of β2-amino acids Angewandte Chemie - International Edition. 43: 1235-1238. PMID 14991786 DOI: 10.1002/Anie.200353000 |
0.373 |
|
2004 |
Sibi MP, Ma Z, Jasperse CP. Exo selective enantioselective nitrone cycloadditions. Journal of the American Chemical Society. 126: 718-9. PMID 14733537 DOI: 10.1021/Ja039087P |
0.395 |
|
2004 |
Sibi MP, Prabagaran N. Chiral relay in enantioselective conjugate radical additions using pyrazolidinone templates. How does metal geometry impact selectivity? Synlett. 2421-2424. DOI: 10.1055/S-2004-832832 |
0.414 |
|
2004 |
Sibi MP, Subramanian T. An enantioselective total synthesis of (-)-stemoamide Synlett. 1211-1214. DOI: 10.1055/S-2004-822927 |
0.412 |
|
2004 |
Sibi MP, Matsunaga H. Enantioselective Diels-Alder reactions of 3-(acyloxy)acrylates Tetrahedron Letters. 45: 5925-5929. DOI: 10.1016/J.Tetlet.2004.05.090 |
0.448 |
|
2004 |
Sibi MP, Stanley LM. Enantioselective diethylzinc additions to aldehydes catalyzed by chiral relay ligands Tetrahedron Asymmetry. 15: 3353-3356. DOI: 10.1016/J.Tetasy.2004.09.006 |
0.678 |
|
2004 |
Sibi MP, Patil K, Rheault TR. Synthesis of Oxacycles by Tandem Radical Addition-Cyclization Reactions European Journal of Organic Chemistry. 372-384. DOI: 10.1002/Ejoc.200300063 |
0.78 |
|
2004 |
Manyem S, Sibi MP. The nature, limits, and implications of asymmetric autocatalysis Chemtracts. 17: 255-260. |
0.738 |
|
2003 |
Sibi MP, Zimmerman J, Rheault T. Enantioselective conjugate radical addition to β-acyloxy acrylate acceptors: An approach to acetate aldol-type products Angewandte Chemie - International Edition. 42: 4521-4523. PMID 14520755 DOI: 10.1002/Anie.200352096 |
0.787 |
|
2003 |
Sibi MP, Prabagaran N, Ghorpade SG, Jasperse CP. Enantioselective synthesis of α,β-disubstituted-β-amino acids Journal of the American Chemical Society. 125: 11796-11797. PMID 14505383 DOI: 10.1021/Ja0372309 |
0.361 |
|
2003 |
Sibi MP, Manyem S, Zimmerman J. Enantioselective radical processes. Chemical Reviews. 103: 3263-96. PMID 12914498 DOI: 10.1021/Cr020044L |
0.78 |
|
2003 |
Sibi MP, Zhang R, Manyem S. A new class of modular chiral ligands with fluxional groups Journal of the American Chemical Society. 125: 9306-9307. PMID 12889955 DOI: 10.1021/Ja035979D |
0.761 |
|
2003 |
Sibi MP, Aasmul M, Hasegawa H, Subramanian T. Tandem radical reactions and ring-closing metathesis. Application in the synthesis of cyclooctenes. Organic Letters. 5: 2883-6. PMID 12889899 DOI: 10.1021/Ol034924D |
0.448 |
|
2003 |
Corminboeuf O, Quaranta L, Renaud P, Liu M, Jasperse CP, Sibi MP. Chiral relay: A novel strategy for the control and amplification of enantioselectivity in Chiral Lewis acid promoted reactions Chemistry - a European Journal. 9: 28-35. PMID 12506361 DOI: 10.1002/Chem.200390000 |
0.507 |
|
2003 |
Rheault TR, Sibi MP. Radical-mediated annulation reactions Synthesis. 803-819. DOI: 10.1055/S-2003-38674 |
0.755 |
|
2003 |
Sibi MP, Manyem S, Zimmerman J. Enantioselective radical processes Chemical Reviews. 103: 3263-3295. DOI: 10.1021/cr020044l |
0.781 |
|
2003 |
Sibi MP, Petrovic G. Enantioselective radical reactions: The use of metal triflimides as Lewis acids Tetrahedron Asymmetry. 14: 2879-2882. DOI: 10.1016/S0957-4166(03)00543-3 |
0.428 |
|
2003 |
Sibi M. Stereoselective radical reactions Tetrahedron Asymmetry. 14: 2847. DOI: 10.1016/J.Tetasy.2003.08.008 |
0.414 |
|
2003 |
Sibi MP, Manyem S, Subramaniam R. Enantioselective radical allylation reactions using chiral lanthanide Lewis acids Tetrahedron. 59: 10575-10580. DOI: 10.1016/J.Tet.2003.07.019 |
0.817 |
|
2003 |
Manyem S, Zimmerman J, Patil K, Sibi MP. Tin-Free Radical-Mediated C-C Bond Formations Chemtracts. 16: 819-826. DOI: 10.1002/chin.200446285 |
0.758 |
|
2002 |
Sibi MP, Miyabe H. Crotylations of α-carbonyl radicals with crotylstannane Organic Letters. 4: 3435-3438. PMID 12323037 DOI: 10.1021/Ol026510A |
0.485 |
|
2002 |
Sibi MP, Hasegawa H, Ghorpade SR. A convenient method for the conversion of N-acyloxazolidinones to hydroxamic acids Organic Letters. 4: 3343-3346. PMID 12323014 DOI: 10.1021/Ol0263301 |
0.385 |
|
2002 |
Sibi MP, Chen J. Enantioselective conjugate addition of silylketene acetals to β-enamidomalonates. Synthesis of β-amino acid derivatives Organic Letters. 4: 2933-2936. PMID 12182592 DOI: 10.1021/Ol026333D |
0.453 |
|
2002 |
Sibi MP, Manyem S. Lanthanide Lewis acid-mediated enantioselective conjugate radical additions Organic Letters. 4: 2929-2932. PMID 12182591 DOI: 10.1021/Ol026327H |
0.821 |
|
2002 |
Sibi MP, Rheault TR, Chandramouli SV, Jasperse CP. Acyclic diastereoselection in prochiral radical addition to prochiral olefins. Journal of the American Chemical Society. 124: 2924-30. PMID 11902883 DOI: 10.1021/Ja017510T |
0.769 |
|
2002 |
Sibi MP, Liu P, Ji J, Hajra S, Chen JX. Free-radical-mediated conjugate additions. Enantioselective synthesis of butyrolactone natural products: (-)-Enterolactone, (-)-arctigenin, (-)-isoarctigenin, (-)-nephrosteranic acid, and (-)-roccellaric acid Journal of Organic Chemistry. 67: 1738-1745. PMID 11895386 DOI: 10.1021/jo015501x |
0.332 |
|
2002 |
Sibi MP, Sausker JB. The role of the achiral template in enantioselective transformations. Radical conjugate additions to α-methacrylates followed by hydrogen atom transfer Journal of the American Chemical Society. 124: 984-991. PMID 11829606 DOI: 10.1021/Ja016839B |
0.428 |
|
2002 |
Liu M, Sibi MP. Recent advances in the stereoselective synthesis of β-amino acids Tetrahedron. 58: 7991-8035. DOI: 10.1016/S0040-4020(02)00991-2 |
0.433 |
|
2002 |
Sibi MP, Gorikunti U, Liu M. Temperature dependent reversal of stereochemistry in enantioselective conjugate amine additions Tetrahedron. 58: 8357-8363. DOI: 10.1016/S0040-4020(02)00988-2 |
0.48 |
|
2001 |
Sibi MP, Liu M. Enantioselective conjugate addition of hydroxylamines to pyrazolidinone acrylamides Organic Letters. 3: 4181-4184. PMID 11784172 DOI: 10.1021/Ol016807T |
0.545 |
|
2001 |
Sibi MP, Chen J, Rheault TR. Radical-mediated annulation reactions. A versatile strategy for the preparation of a series of carbocycles Organic Letters. 3: 3679-3681. PMID 11700111 DOI: 10.1021/Ol016597K |
0.775 |
|
2001 |
Sibi MP, Chen J. Enantioselective tandem radical reactions: Vicinal difunctionalization in acyclic systems with control over relative and absolute stereochemistry [15] Journal of the American Chemical Society. 123: 9472-9473. PMID 11562242 DOI: 10.1021/Ja016633A |
0.39 |
|
2001 |
Sibi MP, Venkatraman L, Liu M, Jasperse CP. A new approach to enantiocontrol and enantioselectivity amplification: Chiral relay in Diels-Alder reactions Journal of the American Chemical Society. 123: 8444-8445. PMID 11516313 DOI: 10.1021/Ja016396B |
0.501 |
|
2001 |
Sibi MP, Johnson MD, Punniyamurthy T. Enantioselective synthesis of peperomins A, C, D, and analogs - Examination of diastereoselective cuprate conjugate additions to N-enoyl-4-diphenylmethyl-2-oxazolidinones Canadian Journal of Chemistry. 79: 1546-1555. DOI: 10.1139/V01-130 |
0.57 |
|
2001 |
Sibi MP, Rheault TR, Miyabe H, Patil K, Jasperse CP. Highly diastereoselective radical addition-cyclization strategy: Facile synthesis of substituted furans Comptes Rendus De L'Academie Des Sciences - Series Iic: Chemistry. 4: 581-584. DOI: 10.1016/S1387-1609(01)01279-8 |
0.776 |
|
2000 |
Sibi MP, Liu M. N-Benzylhydroxylamine addition to beta-aryl enoates. Enantioselective synthesis of beta-aryl-beta-amino acid precursors Organic Letters. 2: 3393-6. PMID 11029219 DOI: 10.1021/Ol006500E |
0.335 |
|
2000 |
Sibi MP, Liu P, Johnson MD. A short synthesis of both enantiomers of enterolactone Canadian Journal of Chemistry. 78: 133-138. DOI: 10.1139/V99-220 |
0.389 |
|
2000 |
Sibi MP, Deshpande PK. A new methodology for the synthesis of β-amino acids Journal of the Chemical Society, Perkin Transactions 1. 1461-1466. DOI: 10.1039/A908747H |
0.379 |
|
2000 |
Sibi MP, Rheault TR. Higher selectivity at higher temperatures! Effect of precursor stereochemistry on diastereoselectivity in radical allylations. Insight into the role of the Lewis acid Journal of the American Chemical Society. 122: 8873-8879. DOI: 10.1021/Ja001456J |
0.747 |
|
2000 |
Sibi MP, Manyem S. Enantioselective conjugate additions Tetrahedron. 56: 8033-8061. DOI: 10.1016/S0040-4020(00)00618-9 |
0.803 |
|
1999 |
Sibi MP, Liu M. Stereoselective conjugate additions to enoates. Enantiomer. 4: 575-90. PMID 10672460 |
0.313 |
|
1999 |
Sibi MP, Ji J, Sausker JB, Jasperse CP. Free radical-mediated intermolecular conjugate additions. Effect of the lewis acid, chiral auxiliary, and additives on diastereoselectivity Journal of the American Chemical Society. 121: 7517-7526. DOI: 10.1021/Ja991205E |
0.452 |
|
1999 |
Sibi MP, Rutherford D, Renhowe PA, Li B. Investigations of a nucleophilic alaninol synthon derived from serine Journal of the American Chemical Society. 121: 7509-7516. DOI: 10.1021/Ja9906249 |
0.406 |
|
1999 |
Sibi MP, Porter NA. Enantioselective free radical reactions Accounts of Chemical Research. 32: 163-171. DOI: 10.1021/Ar9600547 |
0.31 |
|
1999 |
Sibi MP, Chen JX, Cook GR. Reversal of stereochemistry in diethylzinc addition to aldehydes by a simple change of the backbone substituent in L-serine derived ligands Tetrahedron Letters. 40: 3301-3304. DOI: 10.1016/S0040-4039(99)00480-3 |
0.352 |
|
1999 |
Sibi MP, Cook GR, Liu P. Enantioselective reduction of ketones. Examination of bifunctional ligands Tetrahedron Letters. 40: 2477-2480. DOI: 10.1016/S0040-4039(99)00281-6 |
0.394 |
|
1998 |
Sibi MP, Shay JJ, Liu M, Jasperse CP. Chiral Lewis acid catalysis in conjugate additions of O-benzylhydroxylamine to unsaturated amides. Enantioselective synthesis of β-amino acid precursors Journal of the American Chemical Society. 120: 6615-6616. DOI: 10.1021/Ja980520I |
0.476 |
|
1997 |
Sibi MP, Ji J. Practical and Efficient Enantioselective Conjugate Radical Additions Journal of Organic Chemistry. 62: 3800-3801. DOI: 10.1021/Jo970558Y |
0.38 |
|
1997 |
Sibi MP, Chandramouli SV. Intermolecular free radical reactions on solid support. Allylation of esters Tetrahedron Letters. 38: 8929-8932. |
0.315 |
|
1996 |
Sibi MP, Ji J, Wu JH, Gürtler S, Porter NA. Chiral Lewis acid catalysis in radical reactions: Enantioselective conjugate radical additions Journal of the American Chemical Society. 118: 9200-9201. DOI: 10.1021/Ja9623929 |
0.388 |
|
1995 |
Sibi MP, Jasperse CP, Ji J. Lewis acid-mediated intermolecular .beta.-selective radical additions to N-enoyloxazolidinones. Journal of the American Chemical Society. 117: 10779-10780. DOI: 10.1021/Ja00148A035 |
0.308 |
|
1995 |
Sibi MP, Deshpande PK, Ji J. A new chiral oxazolidinone derived from diphenylalaninol. Aldol, alkylation, and diels-alder reactions Tetrahedron Letters. 36: 8965-8968. DOI: 10.1016/0040-4039(95)01984-P |
0.343 |
|
1992 |
Sibi MP, Sorum MT, Bender JA, Gaboury JA. A convenient synthesis of 3-alkyltetronic acids from 3-acyltetronic acids Synthetic Communications. 22: 809-816. DOI: 10.1080/00397919208020844 |
0.361 |
|
1992 |
Gribble GW, Keavy DJ, Davis DA, Saulnier MG, Pelcman B, Barden TC, Sibi MP, Olson ER, BelBruno JJ. Syntheses and Diels-Alder cycloaddition reactions of 4H-furo[3,4-b]indoles. A regiospecific Diels-Alder synthesis of ellipticine Journal of Organic Chemistry. 57: 5878-5891. DOI: 10.1021/Jo00048A021 |
0.473 |
|
1992 |
Sibi MP, Christensen JW, Li B, Renhowe PA. A novel thermolytic annulation of an oxazolidinone: An enantiospecific synthesis of (-)-slaframine Journal of Organic Chemistry. 57: 4329-4330. DOI: 10.1021/Jo00042A002 |
0.342 |
|
1992 |
Sibi MP, Gaboury JA. Application of enzymatic methods to the synthesis of 5-substituted-2-furanones Tetrahedron Letters. 33: 5681-5684. DOI: 10.1016/0040-4039(92)89004-V |
0.332 |
|
1987 |
Sibi MP, Shankaran K, Alo BI, Hahn WR, Snieckus V. Overriding normal Friedel-Crafts regiochemistry in cycliacylation. Regiospecific carbodesilylation and Parham cyclization routes to 7-methoxy-1-indanols Tetrahedron Letters. 28: 2933-2936. DOI: 10.1016/S0040-4039(00)96247-6 |
0.355 |
|
1986 |
SIBI MP, CHATTOPADHYAY S, DANKWARDT JW, SNIECKUS V. ChemInform Abstract: Combinational O-Aryl Carbamate and Benzamide Directed Ortho Metalation Reactions. Chemischer Informationsdienst. 17. DOI: 10.1002/chin.198607320 |
0.338 |
|
1986 |
Sibi MP, Dankwardt JW, Snieckus V. Anionic aromatic ring annelation of o-allylbenzamides. Regiospecific synthesis of naphthols and naphthoquinones Journal of Organic Chemistry. 51: 271-273. |
0.326 |
|
1985 |
Mills RJ, Horvath RF, Sibi MP, Snieckus V. Dilithiated synthons of tertiary benzamides, phthalamides, and 0,0′-aryl dicarbamates Tetrahedron Letters. 26: 1145-1148. DOI: 10.1016/S0040-4039(00)98418-1 |
0.396 |
|
1985 |
Gribble GW, LeHoullier CS, Sibi MP, Allen RW. Synthesis and deamination of 7,12-dihydrobenz[a]anthracen-7,12-imines. A new benz[a]anthracene synthesis Journal of Organic Chemistry. 50: 1611-1616. |
0.451 |
|
1985 |
Sibi MP, Chattopadhyay S, Dankwardt JW, Snieckus V. Combinational O-aryl carbamate and benzamide directed ortho metalation reactions. Synthesis of ochratoxin A and ochratoxin B Journal of the American Chemical Society. 107: 6312-6315. |
0.352 |
|
1984 |
Gribble GW, Saulnier MG, Sibi MP, Obaza-Nutaitis JA. Synthesis and Diels-Alder reactions of 1,3-dimethyl-4-(phenylsulfonyl)-4H-furo[3,4-b]indole. A new annulation strategy for the construction of ellipticine and isoellipticine Journal of Organic Chemistry. 49: 4518-4523. DOI: 10.1021/Jo00197A039 |
0.517 |
|
1984 |
Sibi MP, Miah MAJ, Snieckus V. Ortho-lithiated tertiary benzamides. Magnesium transmetalation and synthesis of phthalides and isocoumarins including mellein and kigelin Journal of Organic Chemistry. 49: 737-742. |
0.39 |
|
1983 |
Gribble GW, Sibi MP, Kumar S, Kelly WJ. Synthesis and Deamination of 1,4-Dihydronaphthalen-1,4-imines: A Convenient Naphthalene Synthesis Synthesis. 1983: 502-504. DOI: 10.1055/S-1983-30404 |
0.524 |
|
1983 |
Sibi MP, Snieckus V. The directed ortho lithiation of O-aryl carbamates. An anionic equivalent of the Fries rearrangement Journal of Organic Chemistry. 14: 1935-1937. DOI: 10.1021/Jo00159A040 |
0.398 |
|
1983 |
GRIBBLE GW, SIBI MP, KUMAR S, KELLY WJ. ChemInform Abstract: SYNTHESIS AND DEAMINATION OF 1,4-DIHYDRONAPHTHALEN-1,4-IMINES: A CONVENIENT NAPHTHALENE SYNTHESIS Chemischer Informationsdienst. 14. DOI: 10.1002/chin.198341166 |
0.466 |
|
1983 |
Sibi MP, Snieckus V. The directed ortho lithiation of O-aryl carbamates. An anionic equivalent of the Fries rearrangement Journal of Organic Chemistry. 48: 1935-1937. |
0.302 |
|
1982 |
Gribble GW, Kelly WJ, Sibi MP. Reactions of Sodium Borohydride in Acidic Media; IX1. Deoxygenation of 1,4-Epoxy-1,4-dihydronaphthalenes; A Convenient Naphthalene Synthesis Synthesis. 1982: 143-145. DOI: 10.1055/S-1982-29720 |
0.494 |
|
1982 |
GRIBBLE GW, KELLY WJ, SIBI MP. ChemInform Abstract: REACTIONS OF SODIUM BOROHYDRIDE IN ACIDIC MEDIA; IX. DEOXYGENATION OF 1,4-EPOXY-1,4-DIHYDRONAPHTHALENES; A CONVENIENT NAPHTHALENE SYNTHESIS Chemischer Informationsdienst. 13. DOI: 10.1002/chin.198223142 |
0.501 |
|
1981 |
Gribble GW, Allen RW, LeHoullier CS, Eaton JT, Easton NR, Slayton RI, Sibi MP. Dichlorocarbene-induced deamination of naphthalen-1,4-imines and anthracen-9,10-imines Journal of Organic Chemistry. 46: 1025-1026. DOI: 10.1021/Jo00318A039 |
0.406 |
|
1980 |
Sibi MP, Lichter RL. Nitrogen-15 nuclear magnetic resonance spectroscopy.15N19F coupling constants in fluoropyridines and fluoroanilines Organic Magnetic Resonance. 14: 494-496. DOI: 10.1002/mrc.1270140613 |
0.525 |
|
1979 |
Sibi MP, Lichter RL. Nitrogen-15 nuclear magnetic resonance spectroscopy. Natural-abundance nitrogen-15 chemical shifts of alkyl- and aryl-substituted ureas Journal of Organic Chemistry. 44: 3017-3022. |
0.565 |
|
1977 |
Sibi MP, Lichter RL. Nitrogen-15 nuclear magnetic resonance spectroscopy. Natural-abundance nitrogen-15 chemical shifts of ring-methylated N,N-dimethylanilines. Effect of inhibition of conjugation Journal of Organic Chemistry. 42: 2999-3004. DOI: 10.1021/Jo00438A011 |
0.584 |
|
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