CHIRAL ACETALS - STEREOCONTROLLED SYNTHESES OF 16-HYDROXYEICOSATETRAENOIC, 17-HYDROXYEICOSATETRAENOIC, AND 18-HYDROXYEICOSATETRAENOIC ACIDS, CYTOCHROME-P-450 ARACHIDONATE METABOLITES

Authors
HECKMANN B MIOSKOWSKI C LUMIN S FALCK JR WEI SZ CAPDEVILA JH
Citation
B. Heckmann et al., CHIRAL ACETALS - STEREOCONTROLLED SYNTHESES OF 16-HYDROXYEICOSATETRAENOIC, 17-HYDROXYEICOSATETRAENOIC, AND 18-HYDROXYEICOSATETRAENOIC ACIDS, CYTOCHROME-P-450 ARACHIDONATE METABOLITES, Tetrahedron letters, 37(9), 1996, pp. 1425-1428
Citations number
13
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
37
Issue
9
Year of publication
1996
Pages
1425 - 1428
Database
ISI
SICI code
0040-4039(1996)37:9<1425:CA-SSO>2.0.ZU;2-B
Abstract
Chiral adducts from Grignard or allylsilane additions to 1,3-dioxan/1, 3-dioxolan-4-ones were exploited for the total synthesis of the R- and S-isomers of the title eicosanoids.