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New epoxyisoindolines by intramolecular diels‐alder reactions of some methyl‐substituted allylaryl‐2‐furfurylamines
Author(s) -
Mance Ana Dunja,
ŠindlerKulyk Marija,
Jakopčić KreŠImir,
HergoldBrundić Antonija,
Nagl Ante
Publication year - 1997
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570340437
Subject(s) - chemistry , intramolecular force , diels–alder reaction , medicinal chemistry , organic chemistry , stereochemistry , catalysis
N ‐Alkenyl‐ N ‐(5‐substituted‐2‐furfuryl)‐ N‐p ‐toluidines 1–10 have been selected to study the intramolecular Diels‐Alder reaction of furans. New epoxyisoindolines 11–20 were prepared and fully characterised.