Metallation of N-Substituted β-Lactams. A Method for the Introduction of 3-Substituents into β-Lactams
Author(s) -
Tony Durst,
Michael J. LeBelle
Publication year - 1972
Publication title -
canadian journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.323
H-Index - 68
eISSN - 1480-3291
pISSN - 0008-4042
DOI - 10.1139/v72-509
Subject(s) - lithium diisopropylamide , chemistry , carbanion , electrophile , alkyl , yield (engineering) , halide , aryl , lithium (medication) , tetrahydrofuran , lactam , medicinal chemistry , organic chemistry , deprotonation , catalysis , ion , medicine , materials science , solvent , metallurgy , endocrinology
N-Alkyl and N-aryl β-lactams yield lithio carbanions upon reaction with lithium diisopropylamide in tetrahydrofuran at −78°. These lithio salts react with a variety of electrophiles (e.g. ketones, esters, reactive alkyl halides) to give the 3-substituted derivatives in fair to good yield. The procedure is useful for the preparation of rather complex 3-substituted β-lactams from readily available simple derivatives.
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