Khandare, SP and Prasad, KR (2021) Four-Step Total Synthesis of (+)-Euphococcinine and (±)-Adaline. In: Journal of Organic Chemistry .
PDF
jou_org_che_86-17_12285-12291_2021.pdf - Published Version Restricted to Registered users only Download (1MB) | Request a copy |
|
PDF
jo1c00938_si_001.pdf - Published Supplemental Material Restricted to Registered users only Download (7MB) | Request a copy |
Official URL: https://doi.org/10.1021/acs.joc.1c00938
Abstract
A four-step enantiospecific total synthesis of bicyclic homotropinone alkaloid euphococcinine and a racemic synthesis of adaline were reported. Key reactions in the synthesis are the diastereoselective addition of a Wittig phosphorene to the ketimines derived from Davis-Ellman sulfinamides, ring-closing metathesis, and intramolecular Michael reactions. ©
Item Type: | Journal Article |
---|---|
Publication: | Journal of Organic Chemistry |
Publisher: | American Chemical Society |
Additional Information: | The copyright for this article belongs to American Chemical Society |
Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
Date Deposited: | 03 Dec 2021 07:51 |
Last Modified: | 03 Dec 2021 07:51 |
URI: | http://eprints.iisc.ac.in/id/eprint/70164 |
Actions (login required)
View Item |