Tetrahedron
Synthesis of 2, 2-dialkylcyclopropylamines from β-chloroimines and application towards the synthesis of1-amino-2, 2-dialkylcyclopropane-carboxylic acids
N De Kimpe, P Sulmon, M Boeykens
Index: De Kimpe; Sulmon; Boeykens Tetrahedron, 1991 , vol. 47, # 20-21 p. 3389 - 3406
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Citation Number: 11
Abstract
Base-induced 1, 5-dehydrochlorination of β-chloroimines, having a relatively acidic hydrogen atom at carbon-1 of the N-substituent (eg benzyl, methoxycarbonylmethyl, α- methylbenzyl), afforded N-cyclopropylimines which were easily hydrolyzed into
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Synthesis of 2, 2-dimethyl-1-aminocyclopropanecarboxylic acid from β-chloroimines
[Kimpe, Norbert De; Sulmon, Paul; Schamp, Niceas Tetrahedron Letters, 1989 , vol. 30, # 37 p. 5029 - 5032]