A Unified Approach to ent-Atisane Diterpenes and Related Alkaloids: Synthesis of (−)-Methyl Atisenoate, (−)-Isoatisine, and the Hetidine Skeleton
Author:
Affiliation:
1. The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, United States
Funder
National Science Foundation
National Institutes of Health
Bristol-Myers Squibb
Teva Pharmaceutical Industries
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja507321j
Reference42 articles.
1. Synthetic strategies toward hetidine and hetisine-type diterpenoid alkaloids
2. Terpenoid-Alkaloids: Their Biosynthetic Twist of Fate and Total Synthesis
3. Total Synthesis of (±)-Methyl Atis-16-en-19-oate via Homoallyl−Homoallyl Radical Rearrangement
4. Total Syntheses of (−)-Methyl Atis-16-en-19-oate, (−)-Methyl Kaur-16-en-19-oate, and (−)-Methyl Trachyloban-19-oate by a Combination of Palladium-Catalyzed Cycloalkenylation and Homoallyl−Homoallyl Radical Rearrangement
5. Total Synthesis of Serofendic Acids A and B Employing Tin-Free Homoallyl−Homoallyl Radical Rearrangement
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