Evolution of a Short and Stereocontrolled Synthesis of (+)-7,20-Diisocyanoadociane-Reference-Cited by-同舟云学术

Evolution of a Short and Stereocontrolled Synthesis of (+)-7,20-Diisocyanoadociane

Published:2022-01-06 Issue:2 Volume:87 Page:1398-1420
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Roosen Philipp C.¹,Karns Alexander S.¹,Ellis Bryan D.¹,Vanderwal Christopher D.¹²^ORCID

Affiliation:

1. Department of Chemistry, University of California, 1102 Natural Science II, Irvine, California 92697-2025, United States

2. Department of Pharmaceutical Sciences, University of California, 101 Theory, Suite 101, Irvine, California 92697-3958, United States

Funder

Division of Chemistry

National Institute of Allergy and Infectious Diseases

University of California, Irvine

National Science Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.1c02700

Reference108 articles.

1. Syntheses and biological studies of marine terpenoids derived from inorganic cyanide

2. Marine isocyanides and related natural products ? structure, biosynthesis and ecology

3. A new diisocyanide of novel ring structure from a sponge

4. Schindeler, T. W. Aside from DICA, the only other perhydropyrene ICT that has succumbed to synthesis is 8-isocyanocycloamphilec-10-ene 4, the unnatural enantiomer of which was made by Schindeler and Piers. Ph.D. Dissertation, University of British Columbia, 1998.

5. Total synthesis and absolute configuration of 7,20-diisocyanoadociane

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