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Cycloaddition von α‐( tert ‐Butylthio)acrylonitril an C, N ‐Diphenylnitron
Author(s) -
Döpp Dietrich,
Henseleit Martina
Publication year - 1982
Publication title -
chemische berichte
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 0009-2940
DOI - 10.1002/cber.19821150242
Subject(s) - cycloaddition , chemistry , acrylonitrile , adduct , stereochemistry , 1,3 dipolar cycloaddition , olefin fiber , medicinal chemistry , organic chemistry , catalysis , polymer , copolymer
Cycloaddition of α‐( tert ‐Butylthio)acrylonitrile to C,N ‐Diphenylnitrone The radicophilic olefin 1a undergoes a smooth 1,3‐dipolar cycloaddition to C,N ‐diphenylnitrone ( 4 ) with formation of 5,5‐disubstituted isoxazolidines 5A, B as the major products accompanied by minor amounts of the regioisomeric adducts 6 and 7 . No products other than 1: 1 cycloadducts have been detected.
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