Novel oxepane formation by TiCl4-catalyzed nucleophilic cleavage of 1-alkoxymethyl 6,8-dioxabicyclo[3.2.1]octanes

Authors
Fujiwara, K Amano, A Tokiwano, T Murai, A
Citation
K. Fujiwara et al., Novel oxepane formation by TiCl4-catalyzed nucleophilic cleavage of 1-alkoxymethyl 6,8-dioxabicyclo[3.2.1]octanes, TETRAHEDRON, 56(8), 2000, pp. 1065-1080
Citations number
24
Categorie Soggetti
Chemistry & Analysis","Organic Chemistry/Polymer Science
Journal title
TETRAHEDRON
ISSN journal
00404020 → ACNP
Volume
56
Issue
8
Year of publication
2000
Pages
1065 - 1080
Database
ISI
SICI code
0040-4020(20000218)56:8<1065:NOFBTN>2.0.ZU;2-8
Abstract
Introduction of an alkoxymethyl group at the C1 position in the 6,8-dioxabi cyclo[3.2.1]octane system enabled novel formation of oxepane compounds in T iCl4-catalyzed acetal cleavage reactions. (C) 2000 Elsevier Science Ltd. Al l rights reserved.