A NOVEL REACTION OF COORDINATED VINYLIDENES - COUPLING WITH HYDROGEN-SULFIDE TO GIVE A ETA(1)-THIOALDEHYDE

被引:33
作者
BIANCHINI, C
GLENDENNING, L
PERUZZINI, M
ROMEROSA, A
ZANOBINI, F
机构
关键词
D O I
10.1039/c39940002219
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The Ru-II fragment [(PN P)RuCl2] assists the coupling of phenylacetylene with H2S to give 2-phenylethanethial [PNP = CH3CH2CH2N(CH(2)CH(2)PPh(2))(2)] in a reaction that is initiated by alk-1-yne to vinylidene tautomerism at ruthenium, followed by electrophilic attack of H2S on the vinylidene ligand; P-phenylethanethial is recovered as either eta(1)-S-ligand or endo-6-benzyl-1-thiabicyclo[2.2.1]hept-3-ene ligand, and the latter molecule is formed via a stereoselective Diels-Alder reaction between cyclopentadiene and the eta(1)-2-phenylethanethial complex.
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页码:2219 / 2220
页数:2
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