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Chemistry Letters

REGIOSELECTIVE FUNCTIONALIZATION OF cis-BICYCLO| 3.3. 0| OCTENONE DERIVATIVES. OXYMERCURATION/REDUCTION versus HYDROBORATION/ …

…, A Castelló, ML García, A Moyano, F Serratosa

文献索引:Carceller, Elena; Castello, Assumpta; Garcia, M. Lluisa; Moyano, Albert; Serratosa, Felix Chemistry Letters, 1984 , p. 775 - 778

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被引用次数: 1

摘要

Cyclic acetal groups at the position 8 of the cis-bicyclo| 3.3. 0| octane system may act as regio-and stereoselective control elements, respectively, in hydroboration and oxymercuration reactions. Whereas the regioselectivity observed in hydroborations must be ascribed to homoallylic inductive effects, and leads predominantly to exo, 1, 3-bifunctional relationships, the effect of acetal group in oxymercuration is mainly stereoselective due to ...