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Synthesis of Substituted Indenes from Isovanillin via Claisen Rearrangement and Ring‐Closing Metathesis
Author(s) -
Huang KengShiang,
Wang EngChi
Publication year - 2004
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.200400060
Subject(s) - chemistry , ring closing metathesis , claisen rearrangement , wittig reaction , metathesis , closing (real estate) , ring (chemistry) , salt metathesis reaction , stereochemistry , organic chemistry , political science , law , polymerization , polymer
A new synthesis of substituted indenes was studied. Based on Claisen rearrangement, Wittig reaction and ring‐closing metathesis (RCM), a series of substituted indenes was synthesized from isovanillin in good yields.