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A total synthesis of (+,-)-quinocarcin

A synthetic route via the key intermediate DX-52-1 21 has resulted in the first total synthesis of the complex antitumor antibiotic quinocarcin 1. Salient features include an acyliminium ion-mediated stereoselective construction of a diazabicyclo (3.2.1) octane nucleus, a stereoselective Pictet-Spengler cyclization, and a silver assisted conversion of DX-52-1 to the title compound.(DIAGRAM, TABLE OR GRAPHIC OMITTED...PLEASE SEE DAI)

Identiferoai:union.ndltd.org:RICE/oai:scholarship.rice.edu:1911/16174
Date January 1988
CreatorsNunes, Joseph John
ContributorsFukuyama, T.
Source SetsRice University
LanguageEnglish
Detected LanguageEnglish
TypeThesis, Text
Format172 p., application/pdf

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