Stereocontrol in the synthesis of kainoids

被引：18

作者：

Baldwin, JE

Fryer, AM

Spyvee, MR

Whitehead, RC

Wood, ME

机构：

[1] Dyson Perrins Laboratory, Oxford, OX1 3QY, South Parks Road

来源：

TETRAHEDRON LETTERS | 1996年 / 37卷 / 38期

关键词：

D O I：

10.1016/0040-4039(96)01522-5

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A stereoselective synthesis of acromelic acid analogues is described in which the C-3/C-4 cis-relative stereochemistry is established by a hydroxyl directed heterogeneous catalytic hydrogenation of an enamide. Copyright (C) 1996 Elsevier Science Ltd

引用

页码：6923 / 6924

页数：2

共 6 条

[1] BALDWIN JE, 1995, TETRAHEDRON LETT, V36, P4869
[2] A GREATLY IMPROVED PROCEDURE FOR RUTHENIUM TETRAOXIDE CATALYZED OXIDATIONS OF ORGANIC-COMPOUNDS
CARLSEN, PHJ
KATSUKI, T
MARTIN, VS
SHARPLESS, KB
[J]. JOURNAL OF ORGANIC CHEMISTRY, 1981, 46 (19) : 3936 - 3938
[3] STEREOCONTROLLED DERIVATIZATION OF 3-METHOXYESTRA-1,3,5(10),N-TETRAENES VIA LEWIS ACID PROMOTED PRINS REACTIONS, (N=7,8(9))
KUNZER, H
SAUER, G
WIECHERT, R
[J]. TETRAHEDRON LETTERS, 1991, 32 (06) : 743 - 746
[4] McGeer E. G., 1978, KAINIC ACID TOOL NEU
[5] Recent developments in kainoid amino acid chemistry
Parsons, AF
[J]. TETRAHEDRON, 1996, 52 (12) : 4149 - 4174
[6] SHIOIRI T, 1981, CHEM PHARM BULL, V29, P3249

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