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Spirodialkylation of 3‐(Phenylthio)‐3‐Sulfolene and Subsequent Synthetic Transformations
Author(s) -
Chou ShangShing P.,
Sung ChinChuan
Publication year - 1989
Publication title -
journal of the chinese chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.329
H-Index - 45
eISSN - 2192-6549
pISSN - 0009-4536
DOI - 10.1002/jccs.198900079
Subject(s) - chemistry , yield (engineering) , michael reaction , organic chemistry , medicinal chemistry , catalysis , materials science , metallurgy
3‐(Phenylthio)‐3‐sulfolene (1) underwent spirodialkylation to give products 2 which were desulfonylated to afford the dienes 3. The Diels‐Alder reaction of 3 was achieved for some reactive dienophiles to yield spiro compounds. Compounds 2 were also converted to sulfonyldienes 9 which reacted as Michael acceptors.
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