MECHANISM OF REARRANGEMENT OF PLATINACYCLOBUTANES

被引:48
作者
CASEY, CP
SCHECK, DM
SHUSTERMAN, AJ
机构
[1] Department of Chemistry, University of Wisconsin, Madison
关键词
D O I
10.1021/ja00509a032
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
No crossover products were observed when the rearrangement of dichlorobis(pyridine)(1 -phenylpropane-1,3-diyl)-platinum(lV) (la) to dichlorobis(pyridine)(2-phenylpropane-1,3-diyl)platinum(lV) (2a) was carried out in the presence of either p-tolylcyclopropane or p-methylstyrene. Preparation of dichlorobis(pyridine)(cis-l-phenylpropane-3-d1-1,3-diyl)platinum(IV) (5a) from cis-phenylcyclopropane-2-d1and rearrangement of 5a to the β-phenylplatinacyclobutane 6 both proceeded with complete retention of stereochemistry. © 1979, American Chemical Society. All rights reserved.
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页码:4233 / 4236
页数:4
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