WITTIG OLEFINATION OF METHYL 1S,2R)-1-BENZAMIDO-2-FORMYLCYCLOPROPANECARBOXYLATE - A POWERFUL TOOL FOR THE SYNTHESIS OF NEW CONFORMATIONALLYCONSTRAINED CYCLOPROPYL AMINO-ACIDS
C. Cativiela et al., WITTIG OLEFINATION OF METHYL 1S,2R)-1-BENZAMIDO-2-FORMYLCYCLOPROPANECARBOXYLATE - A POWERFUL TOOL FOR THE SYNTHESIS OF NEW CONFORMATIONALLYCONSTRAINED CYCLOPROPYL AMINO-ACIDS, Tetrahedron, 52(16), 1996, pp. 5881-5888
The behaviour of methyl 1S,2R)-1-benzamido-2-formylcyclopropanecarboxy
late with stabilised and semi-stabilised ylids has been tested in orde
r to evaluate its synthetic utility in the synthesis of cyclopropyl am
ino acids by Wittig olefination. Wittig adducts were further elaborate
d to obtain the corresponding cyclopropyl amino acids in high yields a
nd enantiomerically pure form. Copyright (C) 1996 Elsevier Science Ltd