Practical enantiospecific synthesis of RPR 111905: A novel non-peptide substance P antagonist

被引:10
作者
Mutti, S
Daubie, C
Malpart, J
Radisson, X
机构
[1] Rhone-Poulenc Rorer - Ctr. de R., Chemical Process - 13, Quai Jules Guesde, 94403 Vitry sur Seine
关键词
D O I
10.1016/S0040-4039(96)02017-5
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The synthesis of enantiomerically pure RPR 111905 was achieved in twelve steps with an overall yield of 6.9%. The synthetic strategy was based on a Diels-Alder reaction to generate the bicyclic framework and the asymmetry was introduced by resolution. Copyright (C) 1996 Elsevier Science Ltd
引用
收藏
页码:8743 / 8746
页数:4
相关论文
共 10 条
[1]  
ACHARD D, 1994, Patent No. 14345
[2]  
DAUBIE C, UNPUB TETRAHEDRON LE
[3]  
MAYER SC, 1994, TETRAHEDRON-ASYMMETR, V5, P519
[4]   DIELS-ALDER REACTIVITY OF OXYGENATED DIENES AND FURANS - SYNTHESIS OF OXYGENATED BIPHENYLS [J].
MCDONALD, E ;
SUKSAMRARN, A ;
WYLIE, RD .
JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1, 1979, (07) :1893-1900
[5]   Enantiospecific synthesis of RPR 107880: A new non peptide substance P antagonist [J].
Mutti, S ;
Daubie, C ;
Decalogne, F ;
Fournier, R ;
Rossi, P .
TETRAHEDRON LETTERS, 1996, 37 (18) :3125-3128
[6]   A convenient synthesis of (S)-(+)-2-(2-methoxyphenyl) propanoic acid [J].
Mutti, S ;
Daubie, C ;
Decalogne, F ;
Fournier, R ;
Montuori, O ;
Rossi, P .
SYNTHETIC COMMUNICATIONS, 1996, 26 (12) :2349-2354
[7]   SYNTHESIS OF RPR-100893, PROTOTYPE OF A NEW SERIES OF POTENT AND SELECTIVE NON PEPTIDE NK1 ANTAGONISTS - THE TRIARYLPERHYDROISOINDOLOLS [J].
TABART, M ;
PEYRONEL, JF .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1994, 4 (05) :673-676
[8]  
TOUSSAINT O, 1986, THESIS U PARIS 6
[9]  
1956, ORG SYNTHESES COLL, V4, P192
[10]  
1955, ORG SYNTHESES COLL, V3, P207