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FInfluence of the base stoichiometry on cyclocondensation of N ‐(2‐bromoethyl)phthalimide with lithium ester enolates
Author(s) -
Calmes M.,
Juan E.,
Rolland M.,
Martinez J.
Publication year - 2002
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.5570390436
Subject(s) - phthalimide , chemistry , stoichiometry , lithium (medication) , base (topology) , organic chemistry , medicinal chemistry , medicine , mathematical analysis , mathematics , endocrinology
The cyclocondensation of N ‐(2‐bromoethyl)phthalimide with the enolate of benzyl phenyl acetate afforded two possible compounds depending on the experimental conditions used.