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)
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|
|Additional Information:||Copyright to this article belongs to Council of Scientific & Industrial Research.|
|Department/Centre:||Division of Chemical Sciences > Organic Chemistry|
|Date Deposited:||26 Jun 2008|
|Last Modified:||27 Aug 2008 13:31|
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