AN IMPROVED PROCEDURE FOR AROMATIC CYANATION

被引：167

作者：

TSCHAEN, DM

DESMOND, R

KING, AO

FORTIN, MC

PIPIK, B

KING, S

VERHOEVEN, TR

机构：

[1] Merck Research Laboratories, Department of Process Research, Rahway

来源：

SYNTHETIC COMMUNICATIONS | 1994年 / 24卷 / 06期

关键词：

D O I：

10.1080/00397919408011310

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

An effective method for conversion of aryl bromides to aryl cyanides is described. The procedure involves treatment of the aryl halide with zinc cyanide in the presence of a catalytic amount of palladium (0).

引用

页码：887 / 890

页数：4

共 4 条

[1] DALTON JR, 1979, J ORG CHEM, V44, P4443, DOI 10.1021/jo01338a042
[2] CYANATION OF AROMATIC HALIDES
ELLIS, GP
ROMNEYALEXANDER, TM
[J]. CHEMICAL REVIEWS, 1987, 87 (04) : 779 - 794
[3] SELECTIVE CARBON-CARBON BOND FORMATION VIA TRANSITION-METAL CATALYSIS .8. DOUBLE METAL CATALYSIS IN CROSS-COUPLING REACTION AND ITS APPLICATION TO STEREO-SELECTIVE AND REGIOSELECTIVE SYNTHESIS OF TRISUBSTITUTED OLEFINS
NEGISHI, E
OKUKADO, N
KING, AO
VANHORN, DE
SPIEGEL, BI
[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1978, 100 (07) : 2254 - 2256
[4] NUCLEOPHILIC DISPLACEMENT CATALYZED BY TRANSITION-METAL .9. [PD2(DBA)3].CHCL3-DPPF CATALYZED CYANATION OF ARYL HALIDES AND ARYL TRIFLATES
TAKAGI, K
SASAKI, K
SAKAKIBARA, Y
[J]. BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1991, 64 (04) : 1118 - 1121

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