Total Synthesis of Strempeliopidine and Non-Natural Stereoisomers through a Convergent Petasis Borono–Mannich Reaction-Reference-Cited by-同舟云学术

Total Synthesis of Strempeliopidine and Non-Natural Stereoisomers through a Convergent Petasis Borono–Mannich Reaction

Published:2023-03-23 Issue:13 Volume:145 Page:7278-7287
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Rand Alexander W.¹,Gonzalez Kevin J.¹,Reimann Christopher E.¹,Virgil Scott C.¹,Stoltz Brian M.¹^ORCID

Affiliation:

1. Warren and Katharine Schlinger Laboratory for Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, United States

Funder

National Institute of General Medical Sciences

National Science Foundation

Heritage Medical Research Investigation Program

Merkin Institute for Translational Research

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.2c13146

Reference70 articles.

1. Natural Products as Sources of New Drugs from 1981 to 2014

2. Further biological activities of vincaleukoblastine—an alkaloid isolated from Vinca rosea (L.)

3. Two ultrastructurally distinct tubulin paracrystals induced in sea-urchin eggs by vinblastine sulphate

4. A Remarkable Series of Vinblastine Analogues Displaying Enhanced Activity and an Unprecedented Tubulin Binding Steric Tolerance: C20′ Urea Derivatives

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