Samuel, Manoharan T and Madhava, Madyastha K (1986) A novel conversion of narcotine into a macrolide. In: Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry, 25 (3). p. 227.
Full text not available from this repository. (Request a copy)Abstract
Narcotine (I) was quaternized with 3-bromopropanol; the resulting compound treated with aqueous KOH to give ring cleavage product II, which on lactonization with tosyl chloride and Et3N gave the 14-membered macrolide III.
| Item Type: | Journal Article |
|---|---|
| Publication: | Indian Journal of Chemistry, Section B: Organic Chemistry Including Medicinal Chemistry |
| Publisher: | Council of Scientific & Industrial Research |
| Additional Information: | Copyright to this article belongs to Council of Scientific & Industrial Research. |
| Keywords: | narcotine;macrolide |
| Department/Centre: | Division of Chemical Sciences > Organic Chemistry |
| Date Deposited: | 26 Jun 2008 |
| Last Modified: | 27 Aug 2008 13:31 |
| URI: | http://eprints.iisc.ac.in/id/eprint/14698 |
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