A DIASTEREOSELECTIVE SYNTHESIS OF (2S, 3R, 4S)-2-AMINO-1-CYCLOHEXYL-6-METHYLHEPTANE-3,4-DIOL, THE ABBOTT AMINODIOL

Authors
ALEXANDER CW LIOTTA DC
Citation
Cw. Alexander et Dc. Liotta, A DIASTEREOSELECTIVE SYNTHESIS OF (2S, 3R, 4S)-2-AMINO-1-CYCLOHEXYL-6-METHYLHEPTANE-3,4-DIOL, THE ABBOTT AMINODIOL, Tetrahedron letters, 37(12), 1996, pp. 1961-1964
Citations number
22
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Tetrahedron letters → ACNP
ISSN journal
00404039
Volume
37
Issue
12
Year of publication
1996
Pages
1961 - 1964
Database
ISI
SICI code
0040-4039(1996)37:12<1961:ADSO(3>2.0.ZU;2-M
Abstract
An efficient asymmetric synthesis of the Abbott aminodiol, 1, is descr ibed beginning with the readily-available starting material, L-phenyla lanine.