publication venue for
- Substituted pyrrole synthesis from nitrodienes 2017
- Oxidative ring-contraction of 3H-1-benzazepines to quinoline derivatives. 56. 2015
- Syntheses of nucleosides with a 1′,2′-β-lactam moiety as potential inhibitors of hepatitis C virus NS5B polymerase. 55. 2014
- Syntheses of 1′,2′-cyclopentyl nucleosides as potential antiviral agents. 55. 2014
- Regioselective alkylation reactions of 2,4-diphenyl-3H-1-benzazepine give either 3-alkyl-3H-1-benzazepines or 1-alkyl-1H-1-benzazepines. 55. 2014
- Syntheses of 4′-spirocyclic phosphono-nucleosides as potential inhibitors of hepatitis C virus NS5B polymerase. 55. 2014
- Syntheses of nucleosides with 2′-spirolactam and 2′- spiropyrrolidine moieties as potential inhibitors of hepatitis C virus NS5B polymerase. 55. 2014
- Solid phase synthesis of hydroxamate peptides for histone deacetylase inhibition. 54. 2013
- Synthesis of 10 stereochemically distinct bis-tetrahydrofuran intermediates for creating a library of 64 asimicin stereoisomers. 50. 2009
- Studies toward the duocarmycin prodrugs for the antibody prodrug therapy approach. 50. 2009
- Effect of various acids at different concentrations on the pinacol rearrangement. 43. 2002
- Tandem ring expansion/aldol cyclization of bicyclo[5.4.01, 7]undecanediones. 43. 2002
- Regioselective synthesis of fluoroaldols. Studies toward fluoroepothilones syntheses via antibody catalysis. 41. 2000
- Design and synthesis of histone deacetylase inhibitors: The development of apicidin transition state analogs. 41. 2000
- Synthesis of side chain modified apicidin derivatives: Potent mechanism-based histone deacetylase inhibitors. 41. 2000
- Tryptophan-replacement and indole-modified apicidins: Synthesis of potent and selective antiprotozoal agents. 41. 2000
- Improved syntheses of fluorinated tertiary butylamines. 40. 1999
- A facile entry into the ring system of sativene. 39. 1998
- Inhibition of UDP-Gal mutase and mycobacterial galactan biosynthesis by pyrrolidine analogues of galactofuranose. 38. 1997
- Modular approach to annonaceous acetogenins. total synthesis of asimicin and bullatacin.. 36. 1995
- Synthesis of spiroketal-modified avermectin analogs: 23-nor-23-oxa- and 23-nor-23-thia-avermectins. 35. 1994
- A general approach to γ-lactones via osmium-catalyzed asymmetric dihydroxylation. Synthesis of (-)- and (+)-muricatacin.. 33. 1992
- Synthesis of all four isomers of disparlure using osmium-catalyzed asymmetric dihydroxylation.. 33. 1992
- Synthesis of ring-contracted, 25-nor-6,5-spiroketal-modified avermectin derivatives. 33. 1992
- Stereoselective synthesis of contiguously substituted butyrolactones based on the cyclic allylsulfonium ylide rearrangement. 30. 1989
- Regiochemical preferences in selenoaldehyde cycloadditions. 28. 1987
- Selenofluorenone: Synthesis and cycloaddition chemistry. 28. 1987
- Functionalization of furans via phenacyl sulfides. 26. 1985
- Generation of thioaldehydes via fluoride induced elimination of α-silyldisulfides. 26. 1985
- An improved synthesis of methyl-labeled fatty acids. 17. 1976