DIASTEREOSELECTIVE IODOCARBOCYCLIZATION REACTION OF 8-PHENYLMENTHYL ALLYLMALONATE - AN EFFICIENT PREPARATION OF A SYNTHETIC INTERMEDIATE OFCYCLOPROPANE AMINO-ACIDS

Authors
INOUE T KITAGAWA O OCHIAI O TAGUCHI T
Citation
T. Inoue et al., DIASTEREOSELECTIVE IODOCARBOCYCLIZATION REACTION OF 8-PHENYLMENTHYL ALLYLMALONATE - AN EFFICIENT PREPARATION OF A SYNTHETIC INTERMEDIATE OFCYCLOPROPANE AMINO-ACIDS, Tetrahedron : asymmetry, 6(3), 1995, pp. 691-692
Citations number
12
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear","Chemistry Physical
Journal title
Tetrahedron : asymmetry → ACNP
ISSN journal
09574166
Volume
6
Issue
3
Year of publication
1995
Pages
691 - 692
Database
ISI
SICI code
0957-4166(1995)6:3<691:DIRO8A>2.0.ZU;2-A
Abstract
The iodocarbocyclization of allylmalonate using (-)-d-phenylmenthol as a chiral auxiliary proceeded with high diastereoselectivity to give t he iodomethylcyclopropane dicarboxylic ester in good yield.