SYNTHESIS OF KAINOID ANALOGS

被引：27

作者：

BARRACLOUGH, P ^{[1
]}

HUDHOMME, P ^{[1
]}

SPRAY, CA ^{[1
]}

YOUNG, DW ^{[1
]}

机构：

[1] UNIV SUSSEX,SCH CHEM & MOLEC SCI,BRIGHTON BN1 9QJ,E SUSSEX,ENGLAND

来源：

TETRAHEDRON | 1995年 / 51卷 / 14期

关键词：

D O I：

10.1016/0040-4020(95)00135-U

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

4-oxoproline has been used as a chiral template in a synthesis of kainoid analogues which are epimeric with the parent compound at C-3.

引用

页码：4195 / 4212

页数：18

共 18 条

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[3] BARRACLOUGH P, 1991, J CHEM RES-S, P306
[4] SYNTHESIS OF POTENTIAL AGONISTS AND ANTAGONISTS FOR CENTRAL GLUTAMATE RECEPTORS BY A NOVEL RING SWITCHING PROCESS
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[6] SIMPLE ANALOGS OF ACROMELIC ACID, WHICH ARE HIGHLY-ACTIVE AGONISTS OF KAINATE TYPE NEUROEXCITANT
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[7] SYNTHESIS OF NEW ACROMELIC ACID CONGENERS - NOVEL NEUROEXCITATORY AMINO-ACIDS ACTING ON GLUTAMATE RECEPTOR
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[8] HERDEWIJNP, 1982, CAN J CHEM, V60, P2903
[9] TRANS-3-NORMAL-PROPYL-L-PROLINE IS A HIGHLY FAVORABLE, CONFORMATIONALLY RESTRICTED REPLACEMENT FOR METHIONINE IN THE C-TERMINAL TETRAPEPTIDE OF CHOLECYSTOKININ - STEREOSELECTIVE SYNTHESIS OF 3-ALLYL-L-PROLINE AND 3-NORMAL-PROPYL-L-PROLINE DERIVATIVES FROM 4-HYDROXY-L-PROLINE
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LIN, CW
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[10] ONE POT SYNTHESIS AND CONFORMATION OF N-TERT-BUTYLOXYCARBONYL, O-PHENACYL DERIVATIVES OF PROLINE AND OTHER SECONDARY AMINO-ACIDS
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