Enantioselective Total Synthesis of (+)-Testudinariol A Using a New Nickel-Catalyzed Allenyl Aldehyde Cyclization
Author:
Affiliation:
1. Department of Chemistry, Wayne State University, Detroit, Michigan 48202
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/ja027148y
Reference18 articles.
1. Testudinariol A and B, two unusual triterpenoids from the skin and the mucus of the marine mollusc Pleurobrancus testudinarius
2. Synthesis of (+)-testudinariol A, a triterpene metabolite of the marine mollusc Pleurobrancus testudinarius
3. Triterpenoid total synthesis. Part 6. Synthesis of testudinariols A and B, triterpene metabolites of the marine mollusc Pleurobrancus testudinarius.
4. Formal Total Synthesis of Testudinariol A, a Triterpene withC2Symmetry
5. The Anti-Selective Boron-Mediated Asymmetric Aldol Reaction of Carboxylic Esters
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