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Studies on pyrrolidones. Reactivity of β‐enaminoesters derived from pyroglutamic acid. Synthesis of methyl cyano[l‐methyl‐5‐(5‐methyl[1,3,4]oxadiazol‐2‐yl)pyrrolidin‐2‐ylidene]acetate
Author(s) -
Fasseur Dominique,
Cauliez Pascal,
Couturier Daniel,
Rigo Benoît,
Defretin Sébastien
Publication year - 1996
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.5570330664
Subject(s) - chemistry , pyroglutamic acid , methyl acetate , reactivity (psychology) , organic chemistry , methanol , biochemistry , amino acid , medicine , alternative medicine , pathology
The 5‐methoxycarbonyl group of β‐enaminoesters derived from methyl pyroglutamate was transformed into acids, amides and 1,3,4‐oxadiazole.