PHOTOCHEMICAL CARBON SKELETAL REARRANGEMENT OF THE BAYLIS-HILLMAN PRODUCTS - BETA-C-H ACTIVATION LEADING TO FURANS

Authors
MATSUMOTO S MIKAMI K
Citation
S. Matsumoto et K. Mikami, PHOTOCHEMICAL CARBON SKELETAL REARRANGEMENT OF THE BAYLIS-HILLMAN PRODUCTS - BETA-C-H ACTIVATION LEADING TO FURANS, Synlett, (5), 1998, pp. 469
Citations number
14
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synlett → ACNP
ISSN journal
09365214
Issue
5
Year of publication
1998
Database
ISI
SICI code
0936-5214(1998):5<469:PCSROT>2.0.ZU;2-M
Abstract
Furan ring formation was found in photochemical reaction of the methyl ether of the Baylis-Hillman products. This reaction proceeds via beta -C-H activation of the photo-excited carbonyl compounds.