Corrigendum to "study on the biosynthesis of the notoamides: Pinacol-type rearrangement of the isoprenyl unit in deoxybrevianamide e and 6-hydroxydeoxybrevianamide E" [Tetrahedron Lett. 52 (2011) 6923-6926]
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Kato, Hikaru,Nakamura, Yuichi,Finefield, Jennifer M.,Umaoka, Hideharu,Nakahara, Takashi,Williams, Robert M.,Tsukamoto, Sachiko
The hydroxypyrroloindolenine (Hpi) motif forms the fundamental core of the pentacyclic natural product, brevianamide E, the concise stereoselective synthesis of which, via oxidative cyclization, is described.
Zhao, Liang,May, Jonathan P.,Huang, Jack,Perrin, David M.
supporting information; experimental part
p. 90 - 93
(2012/02/15)
Studies on the Syntheses of Heterocyclic Compounds. Part 876. The Chiral Total Synthesis of Brevianamide E and Deoxybrevianamide E
The chiral total synthesis of brevianamide E (1) and deoxybrevianamide E (2) starting from L-proline is described.Condensation of 2-(1,1,dimethylallyl)-3-dimethylaminomethylindole (3) and (-)-methyl 1,4-dioxoperhydropyrrolopyrazine-3-carboxylate (7
Kametani, Tetsuji,Kanaya, Naoaki,Ihara, Masataka
p. 959 - 963
(2007/10/02)
Asymmetric Total Synthesis of Brevianamide E
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Kametani, Tetsuji,Kanaya, Naoaki,Ihara, Masataka
p. 3974 - 3975
(2007/10/02)
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