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Preparation of Stable Bicyclic Aziridinium Ions and Their Ring-Opening for the Synthesis of Azaheterocycles
Published on: August 22, 2018
Total synthesis of (+)-strictifolione
1Laboratoire de Chimie Organique Associé au CNRS, ESPCI, 10 rue Vauquelin, 75231 Paris, Cedex 05, France.
Organic Letters
|May 24, 2003
Abstract:
[reaction: see text] The synthesis of (+)-strictifolione was achieved from 3-phenylproprionaldehyde by using enantioselective allyltitanations to control the stereogenic centers at C6, C4', and C6' and a cross-methathesis to control the configuration of the double bond at C1'-C2'.
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