AN EFFICIENT ROUTE TO HOMOLOGATED PYRANOSIDIC CONJUGATED ENALS

被引：12

作者：

BURNOUF, C

LOPEZ, JC

LABORDE, MD

OLESKER, A

LUKACS, G

机构：

来源：

TETRAHEDRON LETTERS | 1988年 / 29卷 / 43期

关键词：

D O I：

10.1016/S0040-4039(00)80805-9

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

引用

页码：5533 / 5534

页数：2

共 7 条

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[6] STEREOSPECIFICITY IN DIELS-ALDER REACTIONS OF DIENES AND DIENOPHILES DERIVED FROM METHYL 4,6-O-BENZYLIDENE-ALPHA-D-GLUCOPYRANOSIDE [J].

LOPEZ, JC ;

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LUKACS, G .

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1988, (11) :706-707

[7] STRAIGHTFORWARD ROUTE TO 2-FORMYL AND 3-FORMYL HEX-1-ENOPYRANOSIDES AND HEX-2-ENOPYRANOSIDES AND THEIR HIGHLY STEREOSELECTIVE HETERO DIELS-ALDER REACTION WITH ETHYL VINYL ETHER [J].

LOPEZ, JC ;

LAMEIGNERE, E ;

LUKACS, G .

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1988, (08) :514-515

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