Synthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactions

Authors
Kongsaeree, P Meepowpan, P Thebtaranonth, Y
Citation
P. Kongsaeree et al., Synthesis of both enantiomers of methylenolactocin, nephrosterinic acid and protolichesterinic acid via tandem aldol-lactonization reactions, TETRAHEDR-A, 12(13), 2001, pp. 1913-1922
Citations number
36
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON-ASYMMETRY
ISSN journal
09574166 → ACNP
Volume
12
Issue
13
Year of publication
2001
Pages
1913 - 1922
Database
ISI
SICI code
0957-4166(20010730)12:13<1913:SOBEOM>2.0.ZU;2-1
Abstract
Both forms of the enantiomerically pure methylenolactocin, nephrosterinic a nd protolichesterinic acid have been synthesized via tandem aldol-lactoniza tion reactions from corresponding optically active itaconate-anthracene add ucts. (C) 2001 Elsevier Science Ltd. All rights reserved.