Evolution of a Synthetic Strategy: Total Synthesis of (±)-Welwitindolinone A Isonitrile-Reference-Cited by-同舟云学术

Evolution of a Synthetic Strategy: Total Synthesis of (±)-Welwitindolinone A Isonitrile

Published:2008-01-17 Issue:6 Volume:130 Page:2087-2100
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Reisman Sarah E.¹,Ready Joseph M.¹,Weiss Matthew M.¹,Hasuoka Atsushi¹,Hirata Makoto¹,Tamaki Kazuhiko¹,Ovaska Timo V.¹,Smith Catherine J.¹,Wood John L.¹

Affiliation:

1. Sterling Chemistry Laboratory, Department of Chemistry, Yale University, New Haven, Connecticut 06520-8107

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja076663z

Reference57 articles.

1. Welwitindolinones, Unusual Alkaloids from the Blue-Green Algae Hapalosiphon welwitschii and Westiella intricata. Relationship to Fischerindoles and Hapalinodoles

2. Oxidized Welwitindolinones from Terrestrial Fischerella spp.

3. Rapid Access to the Welwitindolinone Alkaloid Skeleton by Cyclization of Indolecarboxaldehyde Substituted Cyclohexanones

4. Aryllead(IV) Reagents in Synthesis: Formation of the C11 Quaternary Center of N-Methylwelwitindolinone C Isothiocyanate

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