Total syntheses of 6-and 7-azaindole derived GnRH antagonists

被引：37

作者：

Ujjainwalla, F ^{[1
]}

Walsh, TF ^{[1
]}

机构：

[1] Merck Res Labs, Dept Med Chem, Rahway, NJ 07065 USA

来源：

TETRAHEDRON LETTERS | 2001年 / 42卷 / 37期

关键词：

palladium; heteroannulation; azaindole; 2-aminopyridines;

D O I：

10.1016/S0040-4039(01)01322-3

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The palladium(0)-catalyzed heteroannulation of a triethylsilyl alkyne and an ortho-aminoiodopyridine derivative is used as the key step in a highly convergent route to 6- and 7-azaindoles of biological interest. (C) 2001 Elsevier Science Ltd. All rights reserved.

引用

收藏

页码：6441 / 6445

页数：5

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