Topological selectivity in the intramolecular [4 + 1] pyrroline annulation. Formal total stereospecific synthesis of (.+-.)-supinidine, (.+-.)-isoretronecanol, and (.+-.)-trachelanthamidine
METHOD OF MAKING 1-(ACYLOXY)-ALKYL CARBAMATE COMPOUNDS
申请人:XENOPORT, INC.
公开号:US20140243544A1
公开(公告)日:2014-08-28
Methods of preparing carbamate prodrugs of amine-containing drugs are provided. Carbonates useful in the synthesis of the carbamate prodrugs are also provided.
提供了制备胺类药物的氨基甲酸酯前药的方法。还提供了在合成氨基甲酸酯前药中有用的碳酸盐。
[EN] METHOD OF MAKING 1-(ACYLOXY)-ALKYL CARBAMATE COMPOUNDS<br/>[FR] PROCÉDÉ DE FABRICATION DE COMPOSÉS DE CARBAMATE DE 1-(ACYLOXY)ALKYLE
申请人:XENOPORT INC
公开号:WO2014134005A2
公开(公告)日:2014-09-04
Methods of preparing carbamate prodrugs of amine-containing drugs are provided. Carbonates useful in the synthesis of the carbamate prodrugs are also provided.
Topological selectivity in the intramolecular [4 + 1] pyrroline annulation. Formal total stereospecific synthesis of (.+-.)-supinidine, (.+-.)-isoretronecanol, and (.+-.)-trachelanthamidine
作者:Tomas. Hudlicky、James O. Frazier、Gustavo. Seoane、Mark. Tiedje、Ana. Seoane、Lawrence D. Kwart、Chris. Beal
DOI:10.1021/ja00273a033
日期:1986.6
COLEGATE, S. M.;DORLING, P. R.;HUXTABLE, C. R., AUSTRAL. J. CHEM., 1984, 37, N 7, 1503-1509