Year |
Citation |
Score |
2022 |
Dooley CJ, Rychnovsky SD. Asymmetric Total Synthesis of (2)-Hydroxynorneomajucin, a Norsesquiterpene from . Organic Letters. PMID 35499304 DOI: 10.1021/acs.orglett.2c01207 |
0.349 |
|
2021 |
Wheat A, Yu C, Wang X, Burke AM, Chemmama IE, Kaake RM, Baker P, Rychnovsky SD, Yang J, Huang L. Protein interaction landscapes revealed by advanced in vivo cross-linking-mass spectrometry. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 34349018 DOI: 10.1073/pnas.2023360118 |
0.575 |
|
2020 |
Dooley CJ, Burtea A, Mitilian C, Dao WT, Qu B, Salzameda NT, Rychnovsky SD. Using the Competing Enantioselective Conversion Method to Assign the Absolute Configuration of Cyclic Amines with Bode's Acylation Reagents. The Journal of Organic Chemistry. 85: 10750-10759. PMID 32806106 DOI: 10.1021/Acs.Joc.0C01275 |
0.418 |
|
2019 |
Rychnovsky S, Burtea A, DeForest J, Li X. Total Synthesis of (-)-Himeradine A. Angewandte Chemie (International Ed. in English). PMID 31491044 DOI: 10.1002/Anie.201910129 |
0.469 |
|
2019 |
Burns AS, Rychnovsky SD. Total Synthesis and Structure Revision of (-)-Illisimonin A, a Neuroprotective Sesquiterpenoid from the Fruits of . Journal of the American Chemical Society. PMID 31408328 DOI: 10.1021/Jacs.9B05065 |
0.392 |
|
2018 |
Burtea A, Rychnovsky SD. Biosynthesis-Inspired Approach to Kujounin A Using a Stereoselective Tsuji-Trost Alkylation. Organic Letters. 20: 5849-5852. PMID 30192149 DOI: 10.1021/Acs.Orglett.8B02530 |
0.429 |
|
2018 |
DeForest JC, Samame RA, Suryn G, Burtea A, Rychnovsky SD. Second-Generation Synthesis of (+)-Fastigiatine Inspired by Conformational Studies. The Journal of Organic Chemistry. PMID 29943989 DOI: 10.1021/Acs.Joc.8B01144 |
0.827 |
|
2018 |
Brito GA, Della-Felice F, Luo G, Burns AS, Pilli RA, Rychnovsky SD, Krische MJ. Catalytic Enantioselective Allylations of Acetylenic Aldehydes via 2-Propanol-Mediated Reductive Coupling. Organic Letters. PMID 29938513 DOI: 10.1021/Acs.Orglett.8B01776 |
0.399 |
|
2018 |
Burns AS, Ross CC, Rychnovsky SD. Heteroatom-Directed Acylation of Secondary Alcohols To Assign Absolute Configuration. The Journal of Organic Chemistry. PMID 29424546 DOI: 10.1021/Acs.Joc.7B03156 |
0.344 |
|
2017 |
Burtea A, Rychnovsky SD. Determination of the Absolute Configuration of Cyclic Amines with Bode's Chiral Hydroxamic Esters Using the Competing Enantioselective Conversion Method. Organic Letters. PMID 28763223 DOI: 10.1021/Acs.Orglett.7B01748 |
0.459 |
|
2017 |
Burns AS, Wagner AJ, Fulton JL, Young K, Zakarian A, Rychnovsky SD. Determination of the Absolute Configuration of β-Chiral Primary Alcohols Using the Competing Enantioselective Conversion Method. Organic Letters. PMID 28508638 DOI: 10.1021/Acs.Orglett.7B01189 |
0.324 |
|
2016 |
Samame RA, Owens CM, Rychnovsky SD. Concise synthesis of (+)-fastigiatine. Chemical Science. 7: 188-190. PMID 28966768 DOI: 10.1039/C5Sc03262H |
0.813 |
|
2016 |
Hilf JA, Holzwarth MS, Rychnovsky SD. Route to Highly Substituted Pyridines. The Journal of Organic Chemistry. PMID 27579766 DOI: 10.1021/Acs.Joc.6B01370 |
0.813 |
|
2016 |
Bisen S, Seleverstov O, Belani J, Rychnovsky S, Dopico AM, Bukiya AN. Distinct mechanisms underlying cholesterol protection against alcohol-induced BK channel inhibition and resulting vasoconstriction. Biochimica Et Biophysica Acta. 1861: 1756-1766. PMID 27565113 DOI: 10.1016/J.Bbalip.2016.08.013 |
0.716 |
|
2016 |
Wagner AJ, Miller SM, King RP, Rychnovsky SD. Nanomole-Scale Assignment and One-Use Kits for Determining the Absolute Configuration of Secondary Alcohols. The Journal of Organic Chemistry. PMID 27415613 DOI: 10.1021/Acs.Joc.6B00816 |
0.378 |
|
2016 |
Tay GC, Sizemore N, Rychnovsky SD. Stereoselection in Intramolecular Diels-Alder Reactions of 2-Cyano-1-azadienes: Indolizidine and Quinolizidine Synthesis. Organic Letters. PMID 27295460 DOI: 10.1021/Acs.Orglett.6B00881 |
0.442 |
|
2015 |
Yu C, Mao H, Novitsky EJ, Tang X, Rychnovsky SD, Zheng N, Huang L. Gln40 deamidation blocks structural reconfiguration and activation of SCF ubiquitin ligase complex by Nedd8. Nature Communications. 6: 10053. PMID 26632597 DOI: 10.1038/Ncomms10053 |
0.3 |
|
2015 |
Kandur WV, Kao A, Vellucci D, Huang L, Rychnovsky SD. Design of CID-cleavable protein cross-linkers: identical mass modifications for simpler sequence analysis. Organic & Biomolecular Chemistry. 13: 9793-807. PMID 26269432 DOI: 10.1039/C5Ob01410G |
0.762 |
|
2015 |
Perry MA, Hill RR, Leong JJ, Rychnovsky SD. Stereochemical Outcomes in Reductive Cyclizations To Form Spirocyclic Heterocycles. Organic Letters. 17: 3268-71. PMID 26087830 DOI: 10.1021/Acs.Orglett.5B01422 |
0.805 |
|
2015 |
Burke AM, Kandur W, Novitsky EJ, Kaake RM, Yu C, Kao A, Vellucci D, Huang L, Rychnovsky SD. Synthesis of two new enrichable and MS-cleavable cross-linkers to define protein-protein interactions by mass spectrometry. Organic & Biomolecular Chemistry. 13: 5030-7. PMID 25823605 DOI: 10.1039/C5Ob00488H |
0.768 |
|
2015 |
Perry MA, Rychnovsky SD. Generation, structure and reactivity of tertiary organolithium reagents. Natural Product Reports. 32: 517-33. PMID 25475042 DOI: 10.1039/C4Np00125G |
0.651 |
|
2015 |
Samame RA, Owens CM, Rychnovsky SD. Concise synthesis of (+)-fastigiatine Chemical Science. 7: 188-190. DOI: 10.1039/c5sc03262h |
0.816 |
|
2014 |
Kaake RM, Wang X, Burke A, Yu C, Kandur W, Yang Y, Novtisky EJ, Second T, Duan J, Kao A, Guan S, Vellucci D, Rychnovsky SD, Huang L. A new in vivo cross-linking mass spectrometry platform to define protein-protein interactions in living cells. Molecular & Cellular Proteomics : McP. 13: 3533-43. PMID 25253489 DOI: 10.1074/Mcp.M114.042630 |
0.761 |
|
2014 |
Tay GC, Huang CY, Rychnovsky SD. Silyl enol ether Prins cyclization: diastereoselective formation of substituted tetrahydropyran-4-ones. The Journal of Organic Chemistry. 79: 8733-49. PMID 25200563 DOI: 10.1021/Jo501580P |
0.47 |
|
2014 |
Yu C, Kandur W, Kao A, Rychnovsky S, Huang L. Developing new isotope-coded mass spectrometry-cleavable cross-linkers for elucidating protein structures. Analytical Chemistry. 86: 2099-106. PMID 24471733 DOI: 10.1021/Ac403636B |
0.77 |
|
2014 |
Sizemore N, Rychnovsky SD. Studies toward the synthesis of palhinine lycopodium alkaloids: a Morita-Baylis-Hillman/intramolecular Diels-Alder approach. Organic Letters. 16: 688-91. PMID 24456289 DOI: 10.1021/Ol4033495 |
0.413 |
|
2014 |
Wagner AJ, Miller SM, Nguyen S, Lee GY, Rychnovsky SD, Link RD. Undergraduate laboratory experiment to determine absolute configuration using thin-layer chromatography Journal of Chemical Education. 91: 716-721. DOI: 10.1021/Ed4004996 |
0.361 |
|
2013 |
Wagner AJ, Rychnovsky SD. Kinetic analysis of the HBTM-catalyzed esterification of an enantiopure secondary alcohol. Organic Letters. 15: 5504-7. PMID 24128066 DOI: 10.1021/Ol402643N |
0.324 |
|
2013 |
Tay GC, Gesinski MR, Rychnovsky SD. Formation of highly substituted tetrahydropyranones: application to the total synthesis of cyanolide A. Organic Letters. 15: 4536-9. PMID 23962271 DOI: 10.1021/Ol402095G |
0.836 |
|
2013 |
Myers BR, Sever N, Chong YC, Kim J, Belani JD, Rychnovsky S, Bazan JF, Beachy PA. Hedgehog pathway modulation by multiple lipid binding sites on the smoothened effector of signal response. Developmental Cell. 26: 346-57. PMID 23954590 DOI: 10.1016/J.Devcel.2013.07.015 |
0.72 |
|
2013 |
Perry MA, Hill RR, Rychnovsky SD. Trianion synthon approach to spirocyclic heterocycles. Organic Letters. 15: 2226-9. PMID 23594129 DOI: 10.1021/Ol400788Q |
0.626 |
|
2013 |
Cleary L, Mak VW, Rychnovsky SD, Shea KJ, Sizemore N. Origins of regio- and stereochemistry in type 2 intramolecular N-acylnitroso Diels-Alder reactions: a computational study of tether length and substituent effects. The Journal of Organic Chemistry. 78: 4090-8. PMID 23477601 DOI: 10.1021/Jo4004025 |
0.384 |
|
2013 |
Perry MA, Trinidad JV, Rychnovsky SD. Absolute configuration of lactams and oxazolidinones using kinetic resolution catalysts. Organic Letters. 15: 472-5. PMID 23323958 DOI: 10.1021/Ol303239T |
0.578 |
|
2012 |
Miller SM, Samame RA, Rychnovsky SD. Nanomole-scale assignment of configuration for primary amines using a kinetic resolution strategy. Journal of the American Chemical Society. 134: 20318-21. PMID 23210977 DOI: 10.1021/Ja310620C |
0.781 |
|
2012 |
Kristiana I, Luu W, Stevenson J, Cartland S, Jessup W, Belani JD, Rychnovsky SD, Brown AJ. Cholesterol through the looking glass: ability of its enantiomer also to elicit homeostatic responses. The Journal of Biological Chemistry. 287: 33897-904. PMID 22869373 DOI: 10.1074/Jbc.M112.360537 |
0.716 |
|
2012 |
Kao A, Randall A, Yang Y, Patel VR, Kandur W, Guan S, Rychnovsky SD, Baldi P, Huang L. Mapping the structural topology of the yeast 19S proteasomal regulatory particle using chemical cross-linking and probabilistic modeling. Molecular & Cellular Proteomics : McP. 11: 1566-77. PMID 22550050 DOI: 10.1074/Mcp.M112.018374 |
0.783 |
|
2012 |
Perry MA, Morin MD, Slafer BW, Rychnovsky SD. Total synthesis of lepadiformine alkaloids using N-Boc α-amino nitriles as trianion synthons. The Journal of Organic Chemistry. 77: 3390-400. PMID 22413935 DOI: 10.1021/Jo300161X |
0.827 |
|
2011 |
Reilly MK, Rychnovsky SD. DABO Boronates: Stable Heterocyclic Boronic Acid Complexes for Use in Suzuki-Miyaura Cross-Coupling Reactions. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 2011. PMID 24371372 DOI: 10.1055/S-0030-1261218 |
0.735 |
|
2011 |
Wagner AJ, David JG, Rychnovsky SD. Determination of absolute configuration using kinetic resolution catalysts. Organic Letters. 13: 4470-3. PMID 21776975 DOI: 10.1021/Ol201902Y |
0.305 |
|
2011 |
Gesinski MR, Rychnovsky SD. Total synthesis of the cyanolide A aglycon. Journal of the American Chemical Society. 133: 9727-9. PMID 21639102 DOI: 10.1021/Ja204228Q |
0.832 |
|
2011 |
Bukiya AN, Belani JD, Rychnovsky S, Dopico AM. Specificity of cholesterol and analogs to modulate BK channels points to direct sterol-channel protein interactions. The Journal of General Physiology. 137: 93-110. PMID 21149543 DOI: 10.1085/Jgp.201010519 |
0.725 |
|
2011 |
Kao A, Chiu CL, Vellucci D, Yang Y, Patel VR, Guan S, Randall A, Baldi P, Rychnovsky SD, Huang L. Development of a novel cross-linking strategy for fast and accurate identification of cross-linked peptides of protein complexes. Molecular & Cellular Proteomics : McP. 10: M110.002212. PMID 20736410 DOI: 10.1074/Mcp.M110.002212 |
0.775 |
|
2011 |
Bukiya AN, Belani JD, Rychnovsky S, Dopico AM. Correction: Specificity of cholesterol and analogs to modulate BK channels points to direct sterol-channel protein interactions Journal of General Physiology. 137: 391. DOI: 10.1085/jgp.2010105191374c |
0.692 |
|
2010 |
Reilly MK, Rychnovsky SD. Allyl transfer to aldehydes and ketones by Brønsted acid activation of allyl and crotyl 1,3,2-dioxazaborolidines. Organic Letters. 12: 4892-5. PMID 20942379 DOI: 10.1021/Ol1020515 |
0.739 |
|
2010 |
Perry MA, Morin MD, Slafer BW, Wolckenhauer SA, Rychnovsky SD. Fully substituted carbon centers by diastereoselective spirocyclization: stereoselective synthesis of (+)-lepadiformine C. Journal of the American Chemical Society. 132: 9591-3. PMID 20578697 DOI: 10.1021/Ja104250B |
0.805 |
|
2010 |
Vellucci D, Kao A, Kaake RM, Rychnovsky SD, Huang L. Selective enrichment and identification of azide-tagged cross-linked peptides using chemical ligation and mass spectrometry. Journal of the American Society For Mass Spectrometry. 21: 1432-45. PMID 20472459 DOI: 10.1016/J.Jasms.2010.04.004 |
0.785 |
|
2010 |
Nakamura Y, Burke AM, Kotani S, Ziller JW, Rychnovsky SD. Total synthesis of (-)-lycoperine A. Organic Letters. 12: 72-5. PMID 19947619 DOI: 10.1021/Ol902389E |
0.641 |
|
2010 |
Nakamura Y, Burke AM, Kotani S, Ziller JW, Rychnovsky SD. Synthesis of (-)-Lycoperine A Synfacts. 2010: 505-505. DOI: 10.1055/S-0029-1219713 |
0.418 |
|
2010 |
Bukiya AN, Singh AK, Belani JD, Rychnovsky S, Dopico AM. Strict Structural Requirements for Cholesterol to Inhibit BK Channels Point to Specific Steroid-Protein Interactions Biophysical Journal. 98: 622a. DOI: 10.1016/J.Bpj.2009.12.3405 |
0.728 |
|
2010 |
EVANS DA, BARROW JC, WATSON PS, RATZ AM, DINSMORE CJ, EVRARD DA, DE VRIES KM, ELLMAN JA, RYCHNOVSKY SD, LACOUR J. ChemInform Abstract: Approaches to the Synthesis of the Vancomycin Antibiotics. Synthesis of Orienticin C (Bis-dechlorovancomycin) Aglycon (I). Cheminform. 28: no-no. DOI: 10.1002/chin.199734282 |
0.702 |
|
2010 |
EVANS DA, EVRARD DA, RYCHNOVSKY SD, FRUEH T, WHITTINGHAM WG, DEVRIES KM. ChemInform Abstract: A General Approach to the Asymmetric Synthesis of Vancomycin-Related Arylglycines by Enolate Azidation. Cheminform. 23: no-no. DOI: 10.1002/chin.199241229 |
0.431 |
|
2009 |
Gesinski MR, Tadpetch K, Rychnovsky SD. Symmetric macrocycles by a Prins dimerization and macrocyclization strategy. Organic Letters. 11: 5342-5. PMID 19873984 DOI: 10.1021/Ol9022062 |
0.808 |
|
2009 |
Malathong V, Rychnovsky SD. Polyol synthesis with beta-oxyanionic alkyllithium reagents: syntheses of aculeatins A, B, and D. Organic Letters. 11: 4220-3. PMID 19691310 DOI: 10.1021/Ol901623H |
0.794 |
|
2009 |
Bahnck KB, Rychnovsky SD. Formal Synthesis of (-)-Kendomycin Synfacts. 2009: 354-354. DOI: 10.1055/S-0028-1088088 |
0.411 |
|
2009 |
Cheung LL, Marumoto S, Anderson CD, Rychnovsky SD. Synthesis of SCH 351448 Synfacts. 2009: 130-130. DOI: 10.1055/S-0028-1087612 |
0.413 |
|
2009 |
Bahde RJ, Rychnovsky SD. ChemInform Abstract: Cyclization via Carbolithiation of α-Amino Alkyllithium Reagents. Cheminform. 40. DOI: 10.1002/chin.200904135 |
0.79 |
|
2008 |
Gesinski MR, Van Orden LJ, Rychnovsky SD. Lewis Acid-Promoted Mukaiyama Aldol-Prins (MAP) Cyclizations of Acetals, Ketals, α-Acetoxy Ethers, and Orthoformates. Synlett : Accounts and Rapid Communications in Synthetic Organic Chemistry. 2008: 363-366. PMID 20936058 DOI: 10.1055/S-2008-1032053 |
0.796 |
|
2008 |
Tadpetch K, Rychnovsky SD. Rhenium(VII) catalysis of Prins cyclization reactions. Organic Letters. 10: 4839-42. PMID 18816133 DOI: 10.1021/Ol8019204 |
0.781 |
|
2008 |
Bahnck KB, Rychnovsky SD. Formal synthesis of (-)-kendomycin featuring a Prins-cyclization to construct the macrocycle. Journal of the American Chemical Society. 130: 13177-81. PMID 18767844 DOI: 10.1021/Ja805187P |
0.835 |
|
2008 |
Bahde RJ, Rychnovsky SD. Cyclization via carbolithiation of alpha-amino alkyllithium reagents. Organic Letters. 10: 4017-20. PMID 18700774 DOI: 10.1021/Ol801523R |
0.798 |
|
2008 |
Cheung LL, Marumoto S, Anderson CD, Rychnovsky SD. Assignment of absolute configuration to SCH 351448 via total synthesis. Organic Letters. 10: 3101-4. PMID 18543942 DOI: 10.1021/Ol8011474 |
0.8 |
|
2008 |
Belani JD, Rychnovsky SD. A concise synthesis of ent-Cholesterol. The Journal of Organic Chemistry. 73: 2768-73. PMID 18336043 DOI: 10.1021/Jo702694G |
0.769 |
|
2008 |
Belani JD, Rychnovsky SD. Synthesis of ent-Cholesterol Synfacts. 2008: 790-790. DOI: 10.1055/S-2008-1077897 |
0.756 |
|
2008 |
Gesinski MR, Van Orden LJ, Rychnovsky SD. Lewis acid promoted Mukaiyama aldol-Prins (MAP) cyclizations of acetals, ketals, α-acetoxy ethers, and orthoformates Synlett. 363-366. DOI: 10.1055/s-2008-1032053 |
0.781 |
|
2008 |
Cerf E, Gasper R, Belani JD, Rychnovsky S, Chang Xb, Buyse F, Ruysschaert JM. Corrigendum to "Multidrug resistance protein 1 is not associated to detergent-resistant membranes" [Biochem. Biophys. Res. Commun. 355 (2007) 1025-1030] (DOI:10.1016/j.bbrc.2007.02.075) Biochemical and Biophysical Research Communications. 366: 605. DOI: 10.1016/J.Bbrc.2007.12.016 |
0.703 |
|
2007 |
Epand RM, Shulga YV, Timmons HC, Perri AL, Belani JD, Perinpanathan K, Johnson-McIntire LB, Bajjalieh S, Dicu AO, Elias C, Rychnovsky SD, Topham MK. Substrate chirality and specificity of diacylglycerol kinases and the multisubstrate lipid kinase. Biochemistry. 46: 14225-31. PMID 18004883 DOI: 10.1021/Bi701584V |
0.72 |
|
2007 |
Tian X, Rychnovsky SD. Synthesis and structural reassignment of (+)-epicalyxin F. Organic Letters. 9: 4955-8. PMID 17958435 DOI: 10.1021/Ol702200T |
0.504 |
|
2007 |
Huckins JR, de Vicente J, Rychnovsky SD. Synthesis of the C1-C52 fragment of amphidinol 3, featuring a beta-alkoxy alkyllithium addition reaction. Organic Letters. 9: 4757-60. PMID 17944478 DOI: 10.1021/Ol7020934 |
0.805 |
|
2007 |
Van Orden LJ, Patterson BD, Rychnovsky SD. Total synthesis of leucascandrolide a: a new application of the Mukaiyama aldol-Prins reaction. The Journal of Organic Chemistry. 72: 5784-93. PMID 17595145 DOI: 10.1021/Jo070901R |
0.824 |
|
2007 |
La Cruz TE, Rychnovsky SD. A reductive cyclization approach to attenol A. The Journal of Organic Chemistry. 72: 2602-11. PMID 17346087 DOI: 10.1021/Jo0626459 |
0.824 |
|
2007 |
Cerf E, Gasper R, Belani JD, Rychnovsky S, Chang XB, Buyse F, Ruysschaert JM. Multidrug resistance protein 1 is not associated to detergent-resistant membranes. Biochemical and Biophysical Research Communications. 355: 1025-30. PMID 17336270 DOI: 10.1016/J.Bbrc.2007.02.075 |
0.715 |
|
2007 |
Vellucci D, Rychnovsky SD. Diastereoselective synthesis of the pectenotoxin 2 non-anomeric AB spiroacetal. Organic Letters. 9: 711-4. PMID 17286378 DOI: 10.1021/Ol0630447 |
0.827 |
|
2007 |
Porco, Jr. J, Su S, Lei X, Bardhan S, Rychnovsky S. Synthesis of (+)-Hexacyclinol Synfacts. 2007: 0119-0119. DOI: 10.1055/S-2006-955760 |
0.418 |
|
2006 |
Loening NM, Anderson CE, Iskenderian WS, Anderson CD, Rychnovsky SD, Barfield M, O'Leary DJ. Qualitative and quantitative measurements of hydrogen bond mediated scalar couplings in acyclic 1,3-diols. Organic Letters. 8: 5321-3. PMID 17078708 DOI: 10.1021/Ol062121V |
0.434 |
|
2006 |
Jasti R, Rychnovsky SD. Racemization in Prins cyclization reactions. Journal of the American Chemical Society. 128: 13640-8. PMID 17031979 DOI: 10.1021/Ja064783L |
0.661 |
|
2006 |
de Vicente J, Huckins JR, Rychnovsky SD. Synthesis of the C31-C67 fragment of amphidinol 3. Angewandte Chemie (International Ed. in English). 45: 7258-62. PMID 17013953 DOI: 10.1002/Anie.200602742 |
0.788 |
|
2006 |
Porco JA, Su S, Lei X, Bardhan S, Rychnovsky SD. Total synthesis and structure assignment of (+)-hexacyclinol. Angewandte Chemie (International Ed. in English). 45: 5790-2. PMID 16871643 DOI: 10.1002/Anie.200602854 |
0.573 |
|
2006 |
Bahnck KB, Rychnovsky SD. Rapid stereocontrolled assembly of the fully substituted C-aryl glycoside of kendomycin with a Prins cyclization: a formal synthesis. Chemical Communications (Cambridge, England). 2388-90. PMID 16733589 DOI: 10.1039/B602937J |
0.814 |
|
2006 |
Jasti R, Rychnovsky SD. Solvolysis of a tetrahydropyranyl mesylate: mechanistic implications for the Prins cyclization, 2-oxonia-cope rearrangement, and Grob fragmentation. Organic Letters. 8: 2175-8. PMID 16671810 DOI: 10.1021/Ol0606738 |
0.684 |
|
2006 |
Tian X, Jaber JJ, Rychnovsky SD. Synthesis and structure revision of calyxin natural products. The Journal of Organic Chemistry. 71: 3176-83. PMID 16599616 DOI: 10.1021/Jo060094G |
0.763 |
|
2006 |
La Cruz TE, Rychnovsky SD. Stereoselectivity of intramolecular SN' cyclizations of alkyllithium reagents on methoxy alkenes. The Journal of Organic Chemistry. 71: 1068-73. PMID 16438522 DOI: 10.1021/Jo052166U |
0.819 |
|
2006 |
Rychnovsky S, Tian X, Jaber J. Synthesis of Calyxin L Synfacts. 2006: 0978-0978. DOI: 10.1055/s-2006-949315 |
0.417 |
|
2005 |
Anderson CE, Britt DK, Sangji S, O'Leary DJ, Anderson CD, Rychnovsky SD. Direct assignment of the relative configuration in acyclic 1,3-diols by 1H NMR spectroscopy. Organic Letters. 7: 5721-3. PMID 16321031 DOI: 10.1021/Ol052539D |
0.475 |
|
2005 |
Bolla ML, Patterson B, Rychnovsky SD. Tetrahydropyran rings from a Mukaiyama-Michael cascade reaction. Journal of the American Chemical Society. 127: 16044-5. PMID 16287289 DOI: 10.1021/Ja056483U |
0.823 |
|
2005 |
Anderson CD, Shea KJ, Rychnovsky SD. Strategies for the generation of molecularly imprinted polymeric nitroxide catalysts. Organic Letters. 7: 4879-82. PMID 16235912 DOI: 10.1021/Ol051749N |
0.476 |
|
2005 |
Xu F, Rychnovsky SD, Belani JD, Hobbs HH, Cohen JC, Rawson RB. Dual roles for cholesterol in mammalian cells. Proceedings of the National Academy of Sciences of the United States of America. 102: 14551-6. PMID 16199524 DOI: 10.1073/Pnas.0503590102 |
0.726 |
|
2005 |
Vitale JP, Wolckenhauer SA, Do NM, Rychnovsky SD. Synthesis of the C3-C19 segment of phorboxazole B. Organic Letters. 7: 3255-8. PMID 16018634 DOI: 10.1021/Ol051039H |
0.798 |
|
2005 |
Jasti R, Anderson CD, Rychnovsky SD. Utilization of an oxonia-Cope rearrangement as a mechanistic probe for Prins cyclizations. Journal of the American Chemical Society. 127: 9939-45. PMID 15998101 DOI: 10.1021/Ja0518326 |
0.717 |
|
2005 |
Epand RM, Rychnovsky SD, Belani JD, Epand RF. Role of chirality in peptide-induced formation of cholesterol-rich domains. The Biochemical Journal. 390: 541-8. PMID 15929726 DOI: 10.1042/Bj20050649 |
0.729 |
|
2005 |
Morin MD, Rychnovsky SD. Reductive spiroannulation of nitriles with secondary electrophiles. Organic Letters. 7: 2051-3. PMID 15876052 DOI: 10.1021/Ol050567Q |
0.785 |
|
2005 |
La Cruz TE, Rychnovsky SD. Synthesis of the spirofungin B core by a reductive cyclization strategy. Organic Letters. 7: 1873-5. PMID 15844928 DOI: 10.1021/Ol050589C |
0.82 |
|
2005 |
de Vicente J, Betzemeier B, Rychnovsky SD. A C-glycosidation approach to the central core of amphidinol 3: synthesis of the c39-c52 fragment. Organic Letters. 7: 1853-6. PMID 15844923 DOI: 10.1021/Ol050477L |
0.416 |
|
2005 |
Dalgard JE, Rychnovsky SD. Enantioselective synthesis of the C18-C25 segment of lasonolide A by an oxonia-cope prins cascade. Organic Letters. 7: 1589-91. PMID 15816759 DOI: 10.1021/Ol050270S |
0.82 |
|
2005 |
Takaoka LR, Buckmelter AJ, LaCruz TE, Rychnovsky SD. Rational synthesis of contra-thermodynamic spiroacetals by reductive cyclizations. Journal of the American Chemical Society. 127: 528-9. PMID 15643869 DOI: 10.1021/Ja044642O |
0.829 |
|
2005 |
Graetz B, Rychnovsky S, Leu WH, Farmer P, Lin R. C2-Symmetric nitroxides and their potential as enantioselective oxidants Tetrahedron Asymmetry. 16: 3584-3598. DOI: 10.1016/J.Tetasy.2005.09.016 |
0.781 |
|
2005 |
Wolckenhauer SA, Rychnovsky SD. Stereochemical course of the reductive spiroannulations of N-Boc and N-benzyl 2-cyanopiperidines Tetrahedron. 61: 3371-3381. DOI: 10.1016/J.Tet.2005.01.099 |
0.789 |
|
2004 |
Dalgard JE, Rychnovsky SD. Oxonia-cope prins cyclizations: a facile method for the synthesis of tetrahydropyranones bearing quaternary centers. Journal of the American Chemical Society. 126: 15662-3. PMID 15571386 DOI: 10.1021/Ja044736Y |
0.836 |
|
2004 |
Jasti R, Vitale J, Rychnovsky SD. Axial-selective prins cyclizations by solvolysis of alpha-bromo ethers. Journal of the American Chemical Society. 126: 9904-5. PMID 15303848 DOI: 10.1021/Ja046972E |
0.819 |
|
2004 |
Wolckenhauer SA, Rychnovsky SD. Generation and utility of tertiary alpha-aminoorganolithium reagents. Organic Letters. 6: 2745-8. PMID 15281759 DOI: 10.1021/Ol049039P |
0.809 |
|
2004 |
Dalgard JE, Rychnovsky SD. Memory of chirality in the transannular cyclization of cyclodecenyl radicals. Organic Letters. 6: 2713-6. PMID 15281751 DOI: 10.1021/Ol049038X |
0.79 |
|
2004 |
Kadota I, Hu Y, Packard GK, Rychnovsky SD. A unified approach to polyene macrolides: synthesis of candidin and nystatin polyols. Proceedings of the National Academy of Sciences of the United States of America. 101: 11992-5. PMID 15192147 DOI: 10.1073/Pnas.0401552101 |
0.789 |
|
2004 |
Packard GK, Hu Y, Vescovi A, Rychnovsky SD. Synthesis of rimocidinolide methyl ester, the aglycone of (+)-rimocidin. Angewandte Chemie (International Ed. in English). 43: 2822-6. PMID 15150759 DOI: 10.1002/Anie.200453697 |
0.787 |
|
2004 |
La Cruz TE, Rychnovsky SD. Intramolecular S(N)2' cyclization of an alkyllithium species onto a methoxy allyl ether is syn selective. Chemical Communications (Cambridge, England). 168-9. PMID 14737532 DOI: 10.1039/B314358A |
0.786 |
|
2004 |
Patterson B, Rychnovsky SD. Mukaiyama Aldol-Prins Cyclizations with Ketones Synlett. 543-545. DOI: 10.1055/S-2005-869848 |
0.417 |
|
2004 |
La Cruz TE, Rychnovsky SD. Application of hemithio ketene acetals to the synthesis of spirocyclic orthoesters Synlett. 2013-2015. DOI: 10.1055/S-2004-830874 |
0.829 |
|
2004 |
Jasti R, Vitale J, Rychnovsky SD. Axial-Selective Prins Cyclizations by Solvolysis of α-Bromo Ethers. Cheminform. 35. DOI: 10.1002/chin.200450095 |
0.792 |
|
2004 |
La Cruz TE, Rychnovsky SD. Intramolecular SN2′ cyclization of an alkyllithium species onto a methoxy allyl ether is syn selective Chemical Communications. 10: 168-169. |
0.792 |
|
2003 |
Huckins JR, Rychnovsky SD. Synthesis of optically pure arylsilylcarbinols and their use as chiral auxiliaries in oxacarbenium ion reactions. The Journal of Organic Chemistry. 68: 10135-45. PMID 14682711 DOI: 10.1021/Jo035260O |
0.807 |
|
2003 |
Graetz BR, Rychnovsky SD. Formal synthesis of (-)-apicularen A. Organic Letters. 5: 3357-60. PMID 12943426 DOI: 10.1021/Ol0353417 |
0.819 |
|
2003 |
Patterson B, Marumoto S, Rychnovsky SD. Titanium(IV)-promoted Mukaiyama aldol-Prins cyclizations. Organic Letters. 5: 3163-6. PMID 12917007 DOI: 10.1021/Ol035303N |
0.427 |
|
2003 |
Rychnovsky SD, Cossrow J. Diastereoselective additions of nucleophiles to alpha-acetoxy ethers using the alpha-(trimethylsilyl)benzyl auxiliary. Organic Letters. 5: 2367-70. PMID 12816450 DOI: 10.1021/Ol0347904 |
0.807 |
|
2003 |
Kim AI, Rychnovsky SD. Unified strategy for the synthesis of (-)-elisapterosin B and (-)-colombiasin A. Angewandte Chemie (International Ed. in English). 42: 1267-70. PMID 12645060 DOI: 10.1002/Anie.200390325 |
0.622 |
|
2003 |
Rychnovsky SD, Takaoka LR. Spiroannulation by alkylation and reductive cyclization of nitriles. Angewandte Chemie (International Ed. in English). 42: 818-20. PMID 12596210 DOI: 10.1002/Anie.200390218 |
0.825 |
|
2003 |
Kopecky DJ, Rychnovsky SD. Preparation of α‐Acetoxy Ethers by the Reductive Acetylation of Esters: endo‐1‐Bornyloxyethyl Acetate Organic Syntheses. 80: 177-183. DOI: 10.1002/0471264180.Os080.20 |
0.715 |
|
2003 |
Kopecky DJ, Rychnovsky SD. Preparation of α-acetoxy ethers by the reductive acetylation of esters: Endo-1-bornyloxyethyl acetate (ethanol, 1-[[(1R,2S,4R)-1,7,7- trimethylbicyclo[2.2.1]hept-2-yl]oxy]-, acetate) Organic Syntheses. 80: 177-183. |
0.628 |
|
2002 |
Marumoto S, Jaber JJ, Vitale JP, Rychnovsky SD. Synthesis of (-)-centrolobine by Prins cyclizations that avoid racemization. Organic Letters. 4: 3919-22. PMID 12599492 DOI: 10.1021/Ol026751I |
0.827 |
|
2002 |
Anderson CD, Rychnovsky SD. Empirical model for the molar rotations of syn-2,2-dimethyl-1,3-dioxanes. Organic Letters. 4: 3075-8. PMID 12201720 DOI: 10.1021/Ol0263550 |
0.462 |
|
2002 |
Cossrow J, Rychnovsky SD. Optically pure alpha-(trimethylsilyl)benzyl alcohol: a practical chiral auxiliary for oxocarbenium ion reactions. Organic Letters. 4: 147-50. PMID 11772112 DOI: 10.1021/Ol017063M |
0.805 |
|
2002 |
Sinz CJ, Rychnovsky SD. Total synthesis of the polyene macrolide dermostatin A Tetrahedron. 58: 6561-6576. DOI: 10.1016/S0040-4020(02)00666-X |
0.776 |
|
2001 |
Sinz CJ, Rychnovsky SD. Total Synthesis of Dermostatin A. Angewandte Chemie (International Ed. in English). 40: 3224-3227. PMID 29712036 DOI: 10.1002/1521-3773(20010903)40:17<3224::Aid-Anie3224>3.0.Co;2-D |
0.767 |
|
2001 |
Rychnovsky SD, Marumoto S, Jaber JJ. Role of 2-oxonia Cope rearrangements in Prins cyclization reactions. Organic Letters. 3: 3815-8. PMID 11700146 DOI: 10.1021/Ol0168465 |
0.749 |
|
2001 |
Packard GK, Rychnovsky SD. Beta-selective glycosylations with masked D-mycosamine precursors. Organic Letters. 3: 3393-6. PMID 11594842 DOI: 10.1021/Ol016617I |
0.794 |
|
2001 |
Kopecky DJ, Rychnovsky SD. Mukaiyama aldol-Prins cyclization cascade reaction: a formal total synthesis of leucascandrolide A. Journal of the American Chemical Society. 123: 8420-1. PMID 11516301 DOI: 10.1021/Ja011377N |
0.741 |
|
2001 |
Jaber JJ, Mitsui K, Rychnovsky SD. Stereoselectivity and regioselectivity in the segment-coupling Prins cyclization. The Journal of Organic Chemistry. 66: 4679-86. PMID 11421792 DOI: 10.1021/Jo010232W |
0.77 |
|
2001 |
Rychnovsky SD, Hata T, Kim AI, Buckmelter AJ. Use of a conformational radical clock for evaluating alkyllithium-mediated cyclization reactions. Organic Letters. 3: 807-10. PMID 11263887 DOI: 10.1021/Ol006866R |
0.797 |
|
2001 |
Packard GK, Rychnovsky SD. β-Selective glycosylations with masked D-mycosamine precursors Organic Letters. 3: 3393-3396. DOI: 10.1021/ol016617i |
0.731 |
|
2001 |
Sinz CJ, Rychnovsky SD. Total synthesis of dermostatin A Angewandte Chemie - International Edition. 40: 3224-3227. DOI: 10.1002/1521-3773(20010903)40:17<3224::AID-ANIE3224>3.0.CO;2-D |
0.755 |
|
2000 |
Kopecky DJ, Rychnovsky SD. Improved procedure for the reductive acetylation of acyclic esters and a new synthesis of ethers. The Journal of Organic Chemistry. 65: 191-8. PMID 10813915 DOI: 10.1021/Jo9914521 |
0.73 |
|
2000 |
Rychnovsky SD, Thomas CR. Synthesis of the C22-C26 tetrahydropyran segment of phorboxazole by a stereoselective prins cyclization Organic Letters. 2: 1217-9. PMID 10810711 DOI: 10.1021/Ol005646A |
0.431 |
|
2000 |
Buckmelter AJ, Kim AI, Rychnovsky SD. Conformational memory in enantioselective radical reductions and a new radical clock reaction Journal of the American Chemical Society. 122: 9386-9390. DOI: 10.1021/Ja002068K |
0.752 |
|
2000 |
Rychnovsky SD, Bax BM. Enantioselective reduction of esters: Synthesis of optically active α- acetoxy ethers Tetrahedron Letters. 41: 3593-3596. DOI: 10.1016/S0040-4039(00)00470-6 |
0.818 |
|
1999 |
Rychnovsky SD, Buckmelter AJ, Dahanukar VH, Skalitzky DJ. Synthesis, Equilibration, and Coupling of 4-Lithio-1,3-dioxanes: Synthons for syn- and anti-1,3-Diols. The Journal of Organic Chemistry. 64: 6849-6860. PMID 11674695 DOI: 10.1021/Jo9909352 |
0.781 |
|
1999 |
Powell NA, Rychnovsky SD. Anti-1,3-diols by Addition of Dialkylzinc Reagents to 4-Acetoxy-1,3-dioxanes. The Journal of Organic Chemistry. 64: 2026-2037. PMID 11674297 DOI: 10.1021/Jo982264Y |
0.448 |
|
1999 |
Buckmelter AJ, Powers JP, Rychnovsky SD, Christen DP, Curran DP. Nonequilibrium radical reductions Chemtracts. 12: 635-638. DOI: 10.1021/Ja980857K |
0.728 |
|
1999 |
Richardson TI, Rychnovsky SD. Total synthesis of Filipin III Tetrahedron. 55: 8977-8996. DOI: 10.1021/Ja971916H |
0.368 |
|
1999 |
Rychnovsky SD, Fryszman O, Khire UR. Convergent synthesis of a polyol chain with 4-acetoxy-1,3-dioxanes using a 1,1-bis((trimethylsilyl)methyl)ethene linchpin Tetrahedron Letters. 40: 41-44. DOI: 10.1016/S0040-4039(98)80014-2 |
0.802 |
|
1998 |
Rychnovsky SD, Beauchamp T, Vaidyanathan R, Kwan T. Synthesis of Chiral Nitroxides and an Unusual Racemization Reaction. The Journal of Organic Chemistry. 63: 6363-6374. PMID 11672271 DOI: 10.1021/Jo9808831 |
0.467 |
|
1998 |
Rychnovsky SD, Hu Y, Ellsworth B. Segment-coupling Prins cyclizations Tetrahedron Letters. 39: 7271-7274. DOI: 10.1016/S0040-4039(98)01586-X |
0.339 |
|
1998 |
Rychnovsky SD, Sinz CJ. Diastereoselective synthesis of polypropionates: Cationic couplings of 4-acetoxy-1,3-dioxanes with crotyl-metal reagents Tetrahedron Letters. 39: 6811-6814. DOI: 10.1016/S0040-4039(98)01464-6 |
0.744 |
|
1998 |
Powell NA, Rychnovsky SD. Coupling of alkynyl organometallics with 4-acetoxy-1,3-dioxanes: Synthesis of propargylic and allylic anti-1,3-diols Tetrahedron Letters. 39: 3103-3106. DOI: 10.1016/S0040-4039(98)00512-7 |
0.443 |
|
1997 |
Rychnovsky SD, Yang G, Hu Y, Khire UR. Prins Desymmetrization of a C(2)-Symmetric Diol: Application to the Synthesis of 17-Deoxyroflamycoin. The Journal of Organic Chemistry. 62: 3022-3023. PMID 11671673 DOI: 10.1021/Jo970380F |
0.369 |
|
1997 |
Rychnovsky SD, Powell NA. Dialkylzinc Additions to 4-Acetoxy-1,3-dioxanes: A Highly Stereoselective Route to Protected anti-1,3-Diols Journal of Organic Chemistry. 62: 6460-6461. DOI: 10.1021/Jo971207M |
0.329 |
|
1997 |
Rychnovsky SD, Swenson SS. Alkylation and Reductive Decyanation of 4-Cyano-2,2-dimethyl-1,3-dioxanes (Cyanohydrin Acetonides) Journal of Organic Chemistry. 62: 1333-1340. DOI: 10.1021/Jo961826F |
0.416 |
|
1997 |
Evans DA, Barrow JC, Watson PS, Ratz AM, Dinsmore CJ, Evrard DA, DeVries KM, Ellman JA, Rychnovsky SD, Lacour J. Approaches to the synthesis of the vancomycin antibiotics. Synthesis of orienticin C (bis-dechlorovancomycin) aglycon Journal of the American Chemical Society. 119: 3419-3420. DOI: 10.1021/Ja964420T |
0.788 |
|
1997 |
Rychnovsky SD, Khire UR, Yang G. Total synthesis of the polyene macrolide roflamycoin Journal of the American Chemical Society. 119: 2058-2059. DOI: 10.1021/Ja963800B |
0.411 |
|
1997 |
Rogers BN, Selsted ME, Rychnovsky SD. Synthesis and biological evaluation of non-polyene analogs of amphotericin B Bioorganic and Medicinal Chemistry Letters. 7: 3177-3182. DOI: 10.1016/S0960-894X(97)10180-9 |
0.304 |
|
1997 |
Rychnovsky SD, Swenson SS. Tandem radical nitrile transfer-cyclization reactions of 1,3- dioxane-4-nitriles: Synthesis of spirocyclic systems Tetrahedron. 53: 16489-16502. DOI: 10.1016/S0040-4020(97)01030-2 |
0.416 |
|
1996 |
Dahanukar VH, Rychnovsky SD. General Synthesis of alpha-Acetoxy Ethers from Esters by DIBALH Reduction and Acetylation. The Journal of Organic Chemistry. 61: 8317-8320. PMID 11667826 DOI: 10.1021/Jo961205M |
0.389 |
|
1996 |
Rychnovsky SD, Dahanukar VH. Carbon-Carbon Bond Formation from Small- and Medium-Ring Lactol Acetates via Radical and Oxonium Ion Intermediates. Synthesis of (+/-)-Laurenan. The Journal of Organic Chemistry. 61: 7648-7649. PMID 11667710 DOI: 10.1021/Jo9614349 |
0.318 |
|
1996 |
Richardson TI, Rychnovsky SD. Filipin III: Configuration Assignment and Confirmation by Synthetic Correlation. The Journal of Organic Chemistry. 61: 4219-4231. PMID 11667319 DOI: 10.1021/Jo960218X |
0.352 |
|
1996 |
Hu Y, Skalitzky DJ, Rychnovsky SD. Prins cyclization of 4-allyl-1,3-dioxanes prepared from 1,3-diol synthons. A rapid entry into functionalized tetrahydropyrans Tetrahedron Letters. 37: 8679-8682. DOI: 10.1016/S0040-4039(96)02008-4 |
0.443 |
|
1996 |
Powell NA, Rychnovsky SD. Iodide acceleration in the Pd-catalyzed coupling of aromatic 1,2-ditriflates with alkynes: Synthesis of enediynes Tetrahedron Letters. 37: 7901-7904. DOI: 10.1016/0040-4039(96)01698-X |
0.338 |
|
1996 |
Rychnovsky SD, Dahanukar VH. Oxepanes from an unusual acetal cleavage of 6,8-dioxabicyclo[3.2.1]octanes Tetrahedron Letters. 37: 339-342. DOI: 10.1016/0040-4039(95)02167-1 |
0.373 |
|
1995 |
Rychnovsky SD, Skalitzky DJ. Stereoselective Radical and Cationic Couplings in 4-Acetoxy-1,3-Dioxane Rings Synlett. 1995: 555-556. DOI: 10.1055/S-1995-5281 |
0.339 |
|
1995 |
Rychnovsky SD, Lee JL. A mild, regioselective ketal Claisen rearrangement promoted by triisobutylaluminum Journal of Organic Chemistry. 60: 4318-4319. DOI: 10.1021/Jo00119A005 |
0.357 |
|
1995 |
Beauchamp TJ, Powers JP, Rychnovsky SD. Cascade cyclizations of cyclic sulfates: An enantioselective alternative to polyepoxide cyclizations in the synthesis of poly(tetrahydrofurans) Journal of the American Chemical Society. 117: 12873-12874. DOI: 10.1021/Ja00156A031 |
0.47 |
|
1994 |
Rychnovsky SD, Hwang K. Synthesis of (.+-.)-Combretastatin D-1 and Combretastatin D-2 Journal of Organic Chemistry. 59: 5414-5418. DOI: 10.1021/Jo00097A052 |
0.348 |
|
1994 |
Rychnovsky SD, Hoye RC. Convergent synthesis of the polyene macrolide (-)-roxaticin Journal of the American Chemical Society. 116: 1753-1765. DOI: 10.1021/Ja00084A017 |
0.496 |
|
1994 |
Rychnovsky SD, Hwang K. Synthesis and revised configuration of (+)-combretastatin D-1 Tetrahedron Letters. 35: 8927-8930. DOI: 10.1016/0040-4039(94)88391-2 |
0.314 |
|
1994 |
Rychnovsky SD, Plzak K, Pickering D. Reductive lithiation of alkyl 2-thiopyridyl ethers to generate optically pure α-alkoxylithium reagents Tetrahedron Letters. 35: 6799-6802. DOI: 10.1016/0040-4039(94)85008-9 |
0.379 |
|
1993 |
Rychnovsky SD, Griesgraber G. Convergent synthesis of the spiroacetal fragment of milbemycin β1 Journal of the Chemical Society, Chemical Communications. 291-292. DOI: 10.1039/C39930000291 |
0.319 |
|
1993 |
Poss CS, Rychnovsky SD, Schreiber SL. Two-directional chain synthesis: An application to the synthesis of (+)-mycoticin A Journal of the American Chemical Society. 115: 3360-3361. DOI: 10.1021/Ja00061A057 |
0.527 |
|
1992 |
Rychnovsky SD, Rodriguez C. Synthesis of the polyol chain of (-)-roxaticin Journal of Organic Chemistry. 57: 4793-4795. DOI: 10.1021/Jo00044A007 |
0.373 |
|
1992 |
Rychnovsky SD, Skalitzky DJ. A practical preparation of .alpha.-alkoxylithium reagents: synthesis of syn or anti 1,3-diols Journal of Organic Chemistry. 57: 4336-4339. DOI: 10.1021/Jo00042A005 |
0.412 |
|
1992 |
Rychnovsky SD, Griesgraber G. An iterative and convergent synthesis of syn polyols Journal of Organic Chemistry. 57: 1559-1563. DOI: 10.1021/Jo00031A041 |
0.409 |
|
1992 |
Rychnovsky SD, Powers JP, LePage TJ. Conformation and reactivity of anomeric radicals Journal of the American Chemical Society. 114: 8375-8384. DOI: 10.1021/Ja00048A005 |
0.301 |
|
1992 |
Rychnovsky SD, Skalitzky DJ, Pathirana C, Jensen PR, Fenical W. Stereochemistry of the macrolactins Journal of the American Chemical Society. 114: 671-677. DOI: 10.1021/Ja00028A039 |
0.399 |
|
1992 |
Evans DA, Evrad DA, Rychnovsky SD, Früh T, Whittingham WG, deVries KM. A general approach to the asymmetric synthesis of vancomycin-related arylglycines by enolate azidation Tetrahedron Letters. 33: 1189-1192. DOI: 10.1016/S0040-4039(00)91892-6 |
0.534 |
|
1991 |
Rychnovsky SD, Kim J. Regiospecificity of acetal cleavage to an enol ether using a carbon-13 labeled acetonide Tetrahedron Letters. 32: 7223-7224. DOI: 10.1016/0040-4039(91)80481-K |
0.349 |
|
1991 |
Rychnovsky SD, Kim J. 1-methylcyclopropyl (MCP) ethers as protecting groups Tetrahedron Letters. 32: 7219-7222. DOI: 10.1016/0040-4039(91)80480-T |
0.331 |
|
1990 |
Rychnovsky SD, Zeller S, Skalitzky DJ, Griesgraber G. Stereoselective synthesis of syn-1,3-diol acetonides by reductive decyanation of cyanohydrins Journal of Organic Chemistry. 55: 5550-5551. DOI: 10.1021/Jo00308A004 |
0.466 |
|
1990 |
Rychnovsky SD, Skalitzky DJ. Stereochemistry of alternating polyol chains: 13C NMR analysis of 1,3-diol acetonides Tetrahedron Letters. 31: 945-948. DOI: 10.1016/S0040-4039(00)94399-5 |
0.312 |
|
1989 |
Rychnovsky SD. A convergent synthesis of polyol chains Journal of Organic Chemistry. 54: 4982-4984. DOI: 10.1021/Jo00282A005 |
0.337 |
|
1989 |
Rychnovsky SD, Mickus DE. Preparation of 2-lithiotetrahydropyrans: Kinetic and thermodynamic generation of alkyllithium reagents Tetrahedron Letters. 30: 3011-3014. DOI: 10.1016/S0040-4039(00)99389-4 |
0.351 |
|
1987 |
Stork G, Rychnovsky SD. Iterative butenolide construction of polypropionate chains: Application to an efficient synthesis of (+)(9S)-dihydroerythronolide A Pure and Applied Chemistry. 59: 345-352. DOI: 10.1351/Pac198759030345 |
0.534 |
|
1987 |
Stork G, Rychnovsky SD. Concise total synthesis of (+)-(9S)-dihydroerythronolide A Journal of the American Chemical Society. 109: 1565-1567. DOI: 10.1021/Ja00239A045 |
0.56 |
|
1987 |
Stork G, Rychnovsky SD. Iterative butenolide construction of polypropionate chains Journal of the American Chemical Society. 109: 1564-1565. DOI: 10.1021/Ja00239A044 |
0.452 |
|
1983 |
Stork G, Mook R, Biller SA, Rychnovsky SD. Free-radical cyclization of bromoacetals. Use in the construction of bicyclic acetals and lactones Journal of the American Chemical Society. 105: 3741-3742. DOI: 10.1021/Ja00349A082 |
0.516 |
|
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