2-substituted-3-allenyl-benzo[b]furans through the palladium-catalysed cyclization of propargylic o-(alkynyl)phenyl ethers.

被引：114

作者：

Cacchi, S ^{[1
]}

Fabrizi, G ^{[1
]}

Moro, L ^{[1
]}

机构：

[1] Univ La Sapienza, Dipartimento Studi Chim & Tecnol Sostanze Biol At, I-00185 Rome, Italy

来源：

TETRAHEDRON LETTERS | 1998年 / 39卷 / 28期

关键词：

D O I：

10.1016/S0040-4039(98)00936-8

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The reaction of propargylic o-(alkynyl)phenyl ethers in the presence of' Pd(PPh3)(4) and K2CO3 affords 2-substituted-3-allenylbenzo [b] furans in good yields. Depending on the nature of the starting alkyne, variable amounts of isomeric 2-substituted-3-propargylbenzo[b]furans have bren isolated. (C) 1998 Elsevier Science Ltd. All rights reserved.

引用

页码：5101 / 5104

页数：4

共 15 条

[11] Palladium-catalyzed cyclization of o-alkynyltrifluoroacetanilides with allyl esters. A regioselective synthesis of 3-allylindoles
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[15] SYNTHESIS OF A REBECCAMYCIN-RELATED INDOLO[2,3-A]CARBAZOLE BY PALLADIUM(0) CATALYZED POLYANNULATION
SAULNIER, MG
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