Synthesis via vinyl sulfones 78. Synthesis of 6-carbon termini-differentiated stereotriads via symchiral 2-trifloxy-1,3-cyclohexadiene monoepoxide

Citation
M. Hentemann et Pl. Fuchs, Synthesis via vinyl sulfones 78. Synthesis of 6-carbon termini-differentiated stereotriads via symchiral 2-trifloxy-1,3-cyclohexadiene monoepoxide, TETRAHEDR L, 40(14), 1999, pp. 2699-2702
Citations number
24
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON LETTERS
ISSN journal
00404039 → ACNP
Volume
40
Issue
14
Year of publication
1999
Pages
2699 - 2702
Database
ISI
SICI code
0040-4039(19990402)40:14<2699:SVVS7S>2.0.ZU;2-S
Abstract
Jacobsen epoxidation of 2-trifloxy-1,3-cyclohexadiene provides a valuable a symmetric monoepoxide product that can be readily manipulated to efficientl y provide highly-functionalized symchiral cyclic and acyclic synthons. (C) 1999 Elsevier Science Ltd. All rights reserved.