An expedient palladium-mediated route to 3-arylfurans

被引：0

作者：

Taniguchi, T ^{[1
]}

Nagata, H ^{[1
]}

Kanada, RM ^{[1
]}

Kadota, K ^{[1
]}

Takeuchi, M ^{[1
]}

Ogasawara, K ^{[1
]}

机构：

[1] Tohoku Univ, Inst Pharmaceut, Sendai, Miyagi 9808578, Japan

来源：

HETEROCYCLES | 2000年 / 52卷 / 01期

关键词：

D O I：

暂无

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A facile route to 3-arylfurans has been developed by employing the Heck reaction between 2,5-dihydro-2,5-dimethoxyfuran and aryl iodides as the key step.

引用

页码：67 / 71

页数：5

共 7 条

[1] ORGANOSELENIUM CHEMISTRY - GENERAL FURAN SYNTHESIS [J].

GRIECO, PA ;

POGONOWSKA, CS ;

BURKE, S .

JOURNAL OF ORGANIC CHEMISTRY, 1975, 40 (04) :542-543

[2]

Heck R.F., 1985, PALLADIUM REAGENTS O

[3]

MINATO H, 1965, CHEM IND-LONDON, P899

[4]

SAMIZU K, 1994, HETEROCYCLES, V38, P1745

[5] STUDIES ON FURAN-DERIVATIVES .10. PREPARATION OF 2-METHYLFURO[2,3-C]QUINOLINE DERIVATIVES [J].

USUI, T ;

TSUBONE, Y ;

TANAKA, A .

JOURNAL OF HETEROCYCLIC CHEMISTRY, 1985, 22 (03) :849-852

[6] A general strategy for five-membered heterocycle synthesis by cycloelimination of alkynyl ketones, amides, and thioamides [J].

Wipf, P ;

Rahman, LT ;

Rector, SR .

JOURNAL OF ORGANIC CHEMISTRY, 1998, 63 (21) :7132-7133

[7] 1ST SYNTHESES OF FURO[2,3-C]QUINOLINES THROUGH PD(0)-CATALYZED COUPLING OF FURANBORONIC ACID WITH FUNCTIONALIZED HALOARENES [J].

YANG, YH .

SYNTHETIC COMMUNICATIONS, 1989, 19 (5-6) :1001-1008

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