Stereoselective Reaction for Construction of Quaternary Carbon Center and its Application to the Syntheses of Pyrrolidino[2,3-b]indoline Natural Products-Reference-Cited by-同舟云学术

Stereoselective Reaction for Construction of Quaternary Carbon Center and its Application to the Syntheses of Pyrrolidino[2,3-b]indoline Natural Products

Published:2009 Issue:10 Volume:67 Page:1012-1024
ISSN:0037-9980
Container-title:Journal of Synthetic Organic Chemistry, Japan
language:
Short-container-title:J. Synth. Org. Chem. Jpn.

Author:

Kawasaki Tomomi

Publisher

The Society of Synthetic Organic Chemistry, Japan

Subject

Organic Chemistry

Reference57 articles.

1. 1) ピロロ[2, 3–b]インドールアルカロイドに関する総説: (a) D. Crich, A. Banerjee, Acc. Chem. Res., 40, 151 (2007); (b) T. Hino, M. Nakagawa, Alkaloids, 34, 1 (1988); (c) U. Anthoni, C. Christophersen, P. H. Nielsen, “Alkaloids: Chemical and Biological Perspectives” ed. by S. W. Pelletiesr, Pergamon Press, New York, 1999, Vol. 13, p 163

2. Synthesis of (.+-.)-flustramine B, a marine alkaloid.

3. Synthesis of Isotope Labeled Me(3a)-13C-Physostigmine and Debromoflustramine B

4. Total Synthesis of 5-N-Acetylardeemin and Amauromine: Practical Routes to Potential MDR Reversal Agents

5. Chemistry of Cyclic Tautomers of Tryptophan: Formation of a Quaternary Center at C3a and Total Synthesis of the Marine Alkaloid (+)-ent-Debromoflustramine B

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