Enantioselective Total Synthesis of (−)-Hunterine A Enabled by a Desymmetrization/Rearrangement Strategy-Reference-Cited by-同舟云学术

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Enantioselective Total Synthesis of (−)-Hunterine A Enabled by a Desymmetrization/Rearrangement Strategy

Published:2024-02-12 Issue:7 Volume:146 Page:4340-4345
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Hicks Elliot F.¹,Inoue Kengo¹,Stoltz Brian M.¹^ORCID

Affiliation:

1. The 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 Science Foundation Graduate Research Fellowship Program

National Institute of General Medical Sciences

California Institute of Technology

Heritage Medical Research Investigators Program

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.3c13590

Reference55 articles.

1. Chemistry and biology of monoterpene indole alkaloid biosynthesis

2. The chemistry of mavacurane alkaloids: a rich source of bis-indole alkaloids

3. Rhazinilam–leuconolam family of natural products: a half century of total synthesis

4. Asymmetric Total Synthesis of (+)-Alstonlarsine A

5. Divergent Total Synthesis of Four Kopsane Alkaloids: N ‐Carbomethoxy‐10,22‐dioxokopsane, Epikopsanol‐10‐lactam, 10,22‐Dioxokopsane, and N ‐Methylkopsanone

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Total Synthesis of (–)-Hunterine A;Synfacts;2024-04-15

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