Total Synthesis of (−)-N-Methylwelwitindolinone B Isothiocyanate via a Chlorinative Oxabicycle Ring-Opening Strategy
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, University of California, Los Angeles, California 90095, United States
Funder
Division of Chemistry
National Center for Research Resources
National Institute of General Medical Sciences
Division of Graduate Education
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja5087672
Reference57 articles.
1. Welwitindolinone is well worth it
2. Total Syntheses of the Elusive Welwitindolinones with Bicyclo[4.3.1] Cores
3. TURNING THE CORNER: RECENT ADVANCES IN THE SYNTHESIS OF THE WELWITINDOLINONES
4. Synthetic Studies on N-Methylwelwitindolinone C Isothiocyanate (Welwistatin) and Related Substructures
5. Enantioselective Total Syntheses of Welwitindolinone A and Fischerindoles I and G
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