REGIOCHEMICAL CONTROL OF THE RING-OPENING OF 1,2-EPOXIDES BY MEANS OF CHELATING PROCESSES .9. SYNTHESIS AND RING-OPENING REACTIONS OF CIS-OXIDES AND TRANS-OXIDES DERIVED FROM 3-(BENZYLOXYMETHYL)CYCLOPENTENE AND METHYL 2-CYCLOPENTEN-1-CARBOXYLATE

被引:17
|
作者
COLOMBINI, M [1 ]
CROTTI, P [1 ]
DIBUSSOLO, V [1 ]
FAVERO, L [1 ]
GARDELLI, C [1 ]
MACCHIA, F [1 ]
PINESCHI, M [1 ]
机构
[1] UNIV PISA,DIPARTIMENTO CHIM BIOORGAN,I-56126 PISA,ITALY
关键词
D O I
10.1016/0040-4020(95)00425-8
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The regiochemical outcome of the ring opening of 1,2-epoxides through chelation processes assisted by metal ions, was verified in the oxirane systems derived from cyclopentene bearing a polar functionality (CH(2)OBn or COOMe) in a homoallylic relationship to the oxirane ring. The cis/trans diastereoisomeric epoxide pairs 7-8 and 9-10 derived from 3-(benzyloxymethyl)cyclopentene and methyl 2-cyclopenten-1-carboxylate, respectively, were prepared and some of their opening reactions were studied. The regioselectivity observed turned out to depend on the opening reaction protocol (standard or metal-assisted), suggesting the efficacious incursion, under the appropriate conditions, of chelate bidentate species in the opening process.
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页码:8089 / 8112
页数:24
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