Published in Org Lett on May 21, 2009
Synthesis of highly substituted cyclohexenes via mixed Lewis acid-catalyzed Diels-Alder reactions of highly substituted dienes and dienophiles. Org Lett (2005) 1.03
Anti-lipid-peroxidative principles from Tournefortia sarmentosa. J Nat Prod (2002) 0.99
Total synthesis of (+/-)-morphine. Org Lett (2006) 0.95
Hypoxia-inducible factor-1 inhibitory benzofurans and chalcone-derived diels-alder adducts from Morus species. J Nat Prod (2009) 0.92
New benzo[b]furans as electroluminescent materials for emitting blue light. Org Lett (2005) 0.91
Enantioselective synthesis of (-)-dihydrocodeinone: a short formal synthesis of (-)-morphine. J Org Chem (2006) 0.89
Antioxidant 2-phenylbenzofurans and a coumestan from Lespedeza virgata. J Nat Prod (2008) 0.84
Synthesis of highly substituted cyclohexenes via mixed Lewis acid-catalyzed Diels-Alder reactions of highly substituted dienes and dienophiles. Org Lett (2005) 1.03
Facile synthesis of cis-2-Alkyl-3-trialkylsilyloxycycloalkanones via the non-aldol aldol rearrangement of 2,3-epoxycycloalkanols. Org Lett (2008) 0.82
Stepwise acid-promoted double-Michael process: an alternative to Diels-Alder cycloadditions for hindered silyloxydiene-dienophile pairs. Org Lett (2007) 0.82
First synthesis of the A/B ring of ouabain. Org Lett (2003) 0.80
Total synthesis of auripyrone B using a non-aldol aldol-cuprate opening process. Org Lett (2010) 0.79
Total synthesis of (+/-)-hedychilactone B: stepwise allenoate diene cycloaddition to prepare trimethyldecalin systems. Org Lett (2007) 0.79
Enantiospecific formal total synthesis of (+)-fawcettimine. Org Lett (2010) 0.78
Se-phenyl prop-2-eneselenoate: an ethylene equivalent for Diels-Alder reactions. Angew Chem Int Ed Engl (2013) 0.78
Total synthesis of the proposed structure of mycosporulone: structural revision and an unexpected retro-aldol/aldol reaction. Org Lett (2012) 0.75
Preparation of a functionalized tetracyclic intermediate for the synthesis of rhodexin A. Org Lett (2008) 0.75
An efficient synthesis of the protected carbohydrate moiety of Brasilicardin A. Org Lett (2011) 0.75
Total synthesis of (+/-)-kellermanoldione: stepwise cycloaddition of a functionalized diene and allenoate. Org Lett (2009) 0.75