Synthetic studies of the potent marine toxin, (-)-gymnodimine /

The enantioselective synthesis of the tetrahydrofuran fragment of (-)-gymnodimine, a potent marine neurotoxin, has been achieved in 13% overall yield and 16 steps from 1,3-propanediol. Key features of the convergent synthesis include a chiral auxiliary-mediated, anti-aldol reaction and a substrate c...

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Bibliographic Details

Main Author:	Yang, Ju, 1972-
Format:	Thesis eBook
Language:	English
Published:	[Place of publication not identified] : [publisher not identified] ; 1999.
Subjects:	Major chemistry.
Online Access:	Link to OAKTrust copy