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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >CROWN ETHER CATALYZED STEREOSPECIFIC SYNTHESIS OF Z- AND E-STILBENES BY WITTIG REACTION IN A SOLID-LIQUID TWO-PHASES SYSTEM
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CROWN ETHER CATALYZED STEREOSPECIFIC SYNTHESIS OF Z- AND E-STILBENES BY WITTIG REACTION IN A SOLID-LIQUID TWO-PHASES SYSTEM

机译:固液两相体系中的维氏反应冠醚催化立体定向合成Z-和E-苯乙烯

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摘要

Potassium hydroxide and a catalytic amount of 18-crown-6 are used, in alternative to the classical Wittig conditions, to prepare very rapidly and stereoselectively Z- and E-stilbenes. In particular, the use of benzyltriphenylphosphonium iodides always leads to a complete Z-stereospecificity, while benzyldiphenylchlorophosphonium salts give a complete E-stereospecificity. (C) 1996 Elsevier Science Ltd [References: 17]
机译:除了经典的维蒂希条件外,还使用氢氧化钾和催化量的18-crown-6来制备非常快速且立体选择性的Z-和E-斯蒂苯二酚。特别地,使用苄基三苯基碘化碘总是导致完全的Z-立体特异性,而苄基二苯基氯膦盐给出完全的E-立体特异性。 (C)1996 Elsevier Science Ltd [参考:17]

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