Highly diastereoselective alkylation of 3-substituted tetrahydroisoquinolines

被引:27
作者
Monsees, A
Laschat, S
Dix, I
Jones, PG
机构
[1] Tech Univ Braunschweig, Inst Organ Chem, D-38106 Braunschweig, Germany
[2] Tech Univ Braunschweig, Inst Anorgan & Analyt Chem, D-38106 Braunschweig, Germany
关键词
D O I
10.1021/jo9810967
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
[No abstract available]
引用
收藏
页码:10018 / 10021
页数:4
相关论文
共 22 条
[1]  
[Anonymous], 1972, ISOQUINOLINE ALKALOI
[2]   An enantioselective access to 1-alkyl-1,2-dihydroisoquinolines and 1-alkyl-, 3-alkyl-, and 1,3-dialkyl-1,2,3,4-tetrahydroisoquinolines [J].
Barbier, D ;
Marazano, C ;
Riche, C ;
Das, BC ;
Potier, P .
JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (06) :1767-1772
[3]  
BRAVO P, 1998, EUR J ORG CHEM, V435, P5
[4]  
BRINGMANN G, 1993, LIEBIGS ANN CHEM, P877
[5]  
COMINS DL, 1991, HETEROCYCLES, V32, P1869
[6]   Chiral auxiliary mediated Pictet-Spengler reactions - Asymmetric syntheses of (-)-laudanosine, (+)-glaucine and (-)-xylopinine. [J].
Comins, DL ;
Thakker, PM ;
Baevsky, MF ;
Badawi, MM .
TETRAHEDRON, 1997, 53 (48) :16327-16340
[7]   THE PICTET-SPENGLER CONDENSATION - A NEW DIRECTION FOR AN OLD REACTION [J].
COX, ED ;
COOK, JM .
CHEMICAL REVIEWS, 1995, 95 (06) :1797-1842
[8]   Asymmetric synthesis .41. Totally stereoselective synthesis of 1,3-disubstituted tetrahydroisoquinolines via the CN(R,S) method. [J].
Gosmann, G ;
Guillaume, D ;
Husson, HP .
TETRAHEDRON LETTERS, 1996, 37 (25) :4369-4372
[9]  
Herbert R. B., 1985, CHEM BIOL ISOQUINOLI, P213
[10]  
Kametani T, 1969, CHEM ISOQUINOLINE AL