Zinc(II) promoted conversion of aryltriazenes to aryl iodides and aryl nitriles
摘要:
Aryltriazenes react with zinc perchlorate/zinc cyanide to produces arylnitriles and react with zinc iodide to produce aryliodides. The reaction mechanism involves aryl radicals that have been trapped by addition to propenenitriles in a good preparative Meerwein arylation process. (C) 2001 Elsevier Science Ltd. All rights reserved.
Zinc(II) promoted conversion of aryltriazenes to aryl iodides and aryl nitriles
作者:Timothy B Patrick、Thomas Juehne、Elmer Reeb、Daniel Hennessy
DOI:10.1016/s0040-4039(01)00526-3
日期:2001.5
Aryltriazenes react with zinc perchlorate/zinc cyanide to produces arylnitriles and react with zinc iodide to produce aryliodides. The reaction mechanism involves aryl radicals that have been trapped by addition to propenenitriles in a good preparative Meerwein arylation process. (C) 2001 Elsevier Science Ltd. All rights reserved.