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Waizumi, Nobuaki, Stankovic, Ana R., Rawal, Viresh H. (2003) A General Strategy to Elisabethane Diterpenes:  Stereocontrolled Synthesis of Elisapterosin B via Oxidative Cyclization of an Elisabethin Precursor. Journal Of The American Chemical Society, 125 (43) 13022-13023 doi:10.1021/ja035898h

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Reference TypeJournal (article/letter/editorial)
TitleA General Strategy to Elisabethane Diterpenes:  Stereocontrolled Synthesis of Elisapterosin B via Oxidative Cyclization of an Elisabethin Precursor
JournalJournal Of The American Chemical Society
AuthorsWaizumi, NobuakiAuthor
Stankovic, Ana R.Author
Rawal, Viresh H.Author
Year2003 (October)Volume125
Issue43
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja035898hSearch in ResearchGate
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Mindat Ref. ID1617502Long-form Identifiermindat:1:5:1617502:6
GUID0
Full ReferenceWaizumi, Nobuaki, Stankovic, Ana R., Rawal, Viresh H. (2003) A General Strategy to Elisabethane Diterpenes:  Stereocontrolled Synthesis of Elisapterosin B via Oxidative Cyclization of an Elisabethin Precursor. Journal Of The American Chemical Society, 125 (43) 13022-13023 doi:10.1021/ja035898h
Plain TextWaizumi, Nobuaki, Stankovic, Ana R., Rawal, Viresh H. (2003) A General Strategy to Elisabethane Diterpenes:  Stereocontrolled Synthesis of Elisapterosin B via Oxidative Cyclization of an Elisabethin Precursor. Journal Of The American Chemical Society, 125 (43) 13022-13023 doi:10.1021/ja035898h
In(2003, October) Journal Of The American Chemical Society Vol. 125 (43) American Chemical Society (ACS)

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Sohn, Jeong-Hun, Waizumi, Nobuaki, Zhong, H. Marlon, Rawal, Viresh H. (2005) Total Synthesis of Mycalamide A. Journal Of The American Chemical Society, 127 (20) 7290-7291 doi:10.1021/ja050728l
Kozmin, Sergey A., Rawal, Viresh H. (1998) A General Strategy toAspidospermaAlkaloids:  Efficient, Stereocontrolled Synthesis of Tabersonine. Journal Of The American Chemical Society, 120 (51) 13523-13524 doi:10.1021/ja983198k
Rawal, Viresh H., Michoud, Christophe, Monestel, Robert (1993) General strategy for the stereocontrolled synthesis of Strychnos alkaloids: a concise synthesis of (.+-.)-dehydrotubifoline. Journal Of The American Chemical Society, 115 (7) 3030-3031 doi:10.1021/ja00060a083
Rawal, Viresh H., Dufour, Claire (1994) A General Strategy for Increasing Molecular Complexity: Photocycloaddition-Fragmentation Route to Functionalized Di- and Triquinanes. Journal Of The American Chemical Society, 116 (6) 2613-2614 doi:10.1021/ja00085a049
Rawal, Viresh H., Cava, Michael P. (1986) Photocyclization strategy for the synthesis of antitumor agent CC-1065. Synthesis of the B and C unit fragments. Journal Of The American Chemical Society, 108 (8) 2110-2112 doi:10.1021/ja00268a073
Bhat, Vikram, Rawal, Viresh H. (2011) Stereocontrolled synthesis of 20,21-dihydro N-methylwelwitindolinone B isothiocyanate. Chemical Communications, 47 (34). 9705pp. doi:10.1039/c1cc13498a
Kozmin, Sergey A., Iwama, Tetsuo, Huang, Yong, Rawal, Viresh H. (2002) An Efficient Approach toAspidospermaAlkaloids via [4 + 2] Cycloadditions of Aminosiloxydienes:  Stereocontrolled Total Synthesis of (±)-Tabersonine. Gram-Scale Catalytic Asymmetric Syntheses of (+)-Tabersonine and (+)-16-Methoxytabersonine. Asymmetric Syntheses of (+)-Aspidospermidine and (−)-Quebrachamine. Journal Of The American Chemical Society, 124 (17) 4628-4641 doi:10.1021/ja017863s
Krishnamurthy, Venkat, Rawal, Viresh H. (1998) Novel Routes to Angular and Linear Triquinanes via Radical Induced Epoxide Fragmentation-H-Abstraction-Cyclization Cascades. Journal of the Brazilian Chemical Society, 9. doi:10.1590/s0103-50531998000400006
Yang, Kin S., Rawal, Viresh H. (2014) Synthesis of α-Amino Acid Derivatives and Peptides via Enantioselective Addition of Masked Acyl Cyanides to Imines. Journal Of The American Chemical Society, 136 (46) 16148-16151 doi:10.1021/ja510135t
Xu, Jiasu, Rawal, Viresh H. (2019) Total Synthesis of (−)-Ambiguine P. Journal Of The American Chemical Society, 141 (12) 4820-4823 doi:10.1021/jacs.9b01739
Cassaidy, Kyle J., Rawal, Viresh H. (2021) Enantioselective Total Synthesis of (+)-Heilonine. Journal of the American Chemical Society, 143 (40) 16394-16400 doi:10.1021/jacs.1c08756
 
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