STEREOSELECTIVITY IN REACTIONS OF BICYCLO[3.3.0]OCT-1-ENES

Authors
BOURGIN D BUCHEL R GERBER P KEESE R
Citation
D. Bourgin et al., STEREOSELECTIVITY IN REACTIONS OF BICYCLO[3.3.0]OCT-1-ENES, Tetrahedron letters, 35(20), 1994, pp. 3267-3268
Citations number
22
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
35
Issue
20
Year of publication
1994
Pages
3267 - 3268
Database
ISI
SICI code
0040-4039(1994)35:20<3267:SIROB>2.0.ZU;2-7
Abstract
The derivatives of trans-bicyclo[3.3.0]octane 3 and 6 have been obtain ed the bicyclo[3.3.0]oct-1-enes, sterically hindered at the exo-side, via photoinduced [2+2]cycloaddition of 1 with ethylvinyl ether and by hydroboration-oxidation of 5d, respectively.