Synthetic approaches to anatoxin-a

被引：57

作者：

Mansell, HL

机构：

[1] Wyeth Research (U.K.) Ltd., Huntercombe Lane South, Maidenhead

来源：

TETRAHEDRON | 1996年 / 52卷 / 17期

关键词：

D O I：

10.1016/0040-4020(95)01076-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

[No abstract available]

引用

页码：6025 / 6061

页数：37

共 77 条

[61] A SHORT AND ENANTIOSELECTIVE SYNTHESIS OF (+)-ANATOXIN-A [J].

SOMFAI, P ;

AHMAN, J .

TETRAHEDRON LETTERS, 1992, 33 (26) :3791-3794

[62] A POTENTIAL CARBAPENEM INTERMEDIATE FROM L-GLUTAMIC ACID [J].

SOMFAI, P ;

HUA, MH ;

TANNER, D .

TETRAHEDRON LETTERS, 1991, 32 (02) :283-286

[63] INTRAMOLECULAR REACTIONS OF N-ACYLIMINIUM INTERMEDIATES [J].

SPECKAMP, WN ;

HIEMSTRA, H .

TETRAHEDRON, 1985, 41 (20) :4367-4416

[64] SYNTHESIS OF (+)-ANATOXIN-A AND (-)-ANATOXIN-A VIA CLASSICAL DIASTEREOMERIC SALT RESOLUTION [J].

STJERNLOF, P ;

TROGEN, L ;

ANDERSSON, A .

ACTA CHEMICA SCANDINAVICA, 1989, 43 (09) :917-918

[65] A NEW RING ENLARGEMENT SEQUENCE [J].

STORK, G ;

LANDESMAN, HK .

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1956, 78 (19) :5129-5130

[66]

SWANSON KL, 1991, J PHARMACOL EXP THER, V259, P377

[67]

SWANSON KL, 1990, ACS SYM SER, V418, P107

[68]

TANG HC, 1990, YOUJI HUAXUE, V10, P543

[69] (+)-ANATOXIN-A IS A POTENT AGONIST AT NEURONAL NICOTINIC ACETYLCHOLINE-RECEPTORS [J].

THOMAS, P ;

STEPHENS, M ;

WILKIE, G ;

AMAR, M ;

LUNT, GG ;

WHITING, P ;

GALLAGHER, T ;

PEREIRA, E ;

ALKONDON, M ;

ALBUQUERQUE, EX ;

WONNACOTT, S .

JOURNAL OF NEUROCHEMISTRY, 1993, 60 (06) :2308-2311

[70] CONFORMATIONAL STUDIES ON (+)-ANATOXIN-A AND DERIVATIVES [J].

THOMPSON, PE ;

MANALLACK, DT ;

BLANEY, FE ;

GALLAGHER, T .

JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN, 1992, 6 (03) :287-298

← 1 2 3 4 5 6 7 8 →