Noguchi Michihiko
Affiliate Master
Yamaguchi University
1, 3-dipolar addition of nitrile oxides to 3a, 4-dihydro-1-isoindolinones
Technology reports of the Yamaguchi University Volume 4 Issue 1
Page 43-49
published_at 1987-12
Title
1, 3-dipolar addition of nitrile oxides to 3a, 4-dihydro-1-isoindolinones
Source Identifiers
1,3-Dipolar addition of acetonitrile oxide to 2-phenyl-3a,4-dihydro-1-isoindolinone was carried out in a stereoselective but regiorandam manner. However, the introduction of substituent, e. g., methyl group, at the 4-position of the 1H-isoindol-1-one system turned out to improve regioselectivity of the addition. The regio- and stereoselective isoxazoline synthesis was also accomplished in the reaction with other nitrile oxides. The transformation of the isoxazoline ring was also examined.
Languages
eng
Resource Type
departmental bulletin paper
Publishers
山口大学工学部
Date Issued
1987-12
File Version
Version of Record
Access Rights
open access
Relations
[ISSN]0386-3433
[NCID]AA0086073X
Schools
工学部