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The Total Synthesis of the Annonaceous Acetogenin, Muricatetrocin C
Author(s) -
Dixon Darren J.,
Ley Steven V.,
Reynolds Dominic J.
Publication year - 2000
Publication title -
angewandte chemie international edition
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 1433-7851
DOI - 10.1002/1521-3773(20001016)39:20<3622::aid-anie3622>3.0.co;2-h
Subject(s) - acetogenin , desymmetrization , total synthesis , stereochemistry , chemistry , organic chemistry , annonaceae , biology , enantioselective synthesis , catalysis , botany
A highly diastereoselective hetero‐Diels–Alder reaction , an O–C rearrangement, and a spatial/chemical desymmetrization are three new reactions that have been developed and exploited in the total synthesis of muricatetrocin C, an annonaceous acetogenin.
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