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Total Synthesis of (−)-Kopsifoline A and (+)-Kopsifoline E

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sword-2022-03-10T20:12:25.original.xml (130 B)
Original SWORD entry document
Author(s)
Myeong, In-Soo
•
Avci, Nadide Hazal
•
Movassaghi, Mohammad
Date Issued
December 3, 2021
Journal
Organic Letters
Publisher
American Chemical Society (ACS)
Citation
Myeong, In-Soo, Avci, Nadide Hazal and Movassaghi, Mohammad. 2021. "Total Synthesis of (−)-Kopsifoline A and (+)-Kopsifoline E." Organic Letters, 23 (23).
Version
Original manuscript
Abstract
We report the first total synthesis of (-)-kopsifoline A and (+)-kopsifoline E. Our synthetic strategy features a biogenetically inspired regioselective C17-functionalization of a versatile intermediate containing the pentacyclic core of aspidosperma alkaloids. The vinylogous urethane substructure of this intermediate affords (-)-kopsifoline D via C3-C21 bond formation under the Mitsunobu reaction conditions, while it enables selective C17-functionalization en route to (-)-kopsifoline A and (+)-kopsifoline E.
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Creative Commons Attribution-Noncommercial-Share Alike
http://creativecommons.org/licenses/by-nc-sa/4.0/
Persistent DSpace Link
https://hdl.handle.net/1721.1/141145
DOI of Published Version
10.1021/acs.orglett.1c03448
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