Enantioselective Total Synthesis of (+)-Reserpine
Author:
Affiliation:
1. Department of Chemistry and Chemical Biology, Harvard University, Cambridge, Massachusetts 02138, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol400046n
Reference35 articles.
1. Reserpin, der sedative Wirkstoff ausRauwolfia serpentina Benth
2. Reserpine: A Challenge for Total Synthesis of Natural Products
3. A Torquoselective 6π Electrocyclization Approach to Reserpine Alkaloids
4. Studies towards the synthesis of (±)-reserpine: Photocyclization mediated a novel and efficient synthesis of 11,18-dimethoxy-(20α)-18,19-didehydro-yohimban-17-one
5. An Efficient Synthesis of a Potential (−)-Reserpine Intermediate from (−)-Shikimic Acid of the Chiral Pool
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