A RHODIUM-MEDIATED, STEPWISE TRIMERIZATION OF AN ALKYNE THAT DOES NOT LEAD TO A BENZENE BUT SELECTIVELY TO A HEXADIENYNE DERIVATIVE

被引:55
作者
WERNER, H [1 ]
SCHAFER, M [1 ]
WOLF, J [1 ]
PETERS, K [1 ]
VONSCHNERING, HG [1 ]
机构
[1] MAX PLANCK INST FESTKORPERFORSCH,D-70506 STUTTGART,GERMANY
来源
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH | 1995年 / 34卷 / 02期
关键词
ALKYNETRIMERIZATION; COMPLEXES WITH CARBON LIGANDS; DIENYNES; RHODIUM COMPOUNDS;
D O I
10.1002/anie.199501911
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The coupling of an alkynyl and a butadienyl unit at the rhodium center of 1 is the key step in the selective, stepwise trimerization of methyl propiolate HCCR to hexadienyne 3 with [Rh(η2‐O2CMe)(PiPr3)2] as a metal template. In MgCl2 in ether, this step occurs almost quantitatively, and the intermediates 1 and 2 were characterized by X‐ray crystal structure analysis. (Figure Presented.) Copyright © 1995 by VCH Verlagsgesellschaft mbH, Germany
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页码:191 / 194
页数:4
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