Unified, Biosynthesis-Inspired, Completely Stereocontrolled Total Synthesis of All Highest-Order [n + 1] Oligocyclotryptamine Alkaloids-Reference-Cited by-同舟云学术

Unified, Biosynthesis-Inspired, Completely Stereocontrolled Total Synthesis of All Highest-Order [n + 1] Oligocyclotryptamine Alkaloids

Published:2024-08-12 Issue:33 Volume:146 Page:23574-23581
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Scott Tony Z.¹,Movassaghi Mohammad¹^ORCID

Affiliation:

1. Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States

Funder

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.4c07705

Reference48 articles.

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2. b Hino, T.; Nakagawa, M. The Alkaloids: Chemistry and Pharmacology. Brossi, A., Ed. Academic Press: New York, 1989, Vol. 34, pp. 175.

3. c Sevenet, T.; Pusset, J. The Alkaloids: Chemistry and Pharmacology. Cordell, G. A., Ed. Academic Press: New York, 1996, Vol. 48, pp. 173.

4. d Anthoni, U.; Christophersen, C.; Nielsen, P. H. Alkaloids: Chemical and Biological Perspectives. Pelletier, S. W., Ed. Pergamon: London, 1999, Vol. 13, pp. 163236.

5. Chemistry of the Hexahydropyrrolo[2,3-b]indoles: Configuration, Conformation, Reactivity, and Applications in Synthesis

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1. Unified, Biosynthesis-Inspired, Completely Stereocontrolled Total Synthesis of All Highest-Order [n + 1] Oligocyclotryptamine Alkaloids;Journal of the American Chemical Society;2024-08-12