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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 >3+2 CYCLOADDITION VIA A DIELS-ALDER RETRO-DIELS-ALDER SEQUENCE - TANDEM CYCLOPENTADIENYL ANNULATION OF A 1,5-CYCLOOCTADIYNE SYNTHETIC EQUIVALENT
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3+2 CYCLOADDITION VIA A DIELS-ALDER RETRO-DIELS-ALDER SEQUENCE - TANDEM CYCLOPENTADIENYL ANNULATION OF A 1,5-CYCLOOCTADIYNE SYNTHETIC EQUIVALENT

机译:通过Diels-Alder逆向Diels-Alder序列的3 + 2循环-串联1,5-环戊二烯合成的环戊二烯环化

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摘要

A novel method of synthesizing a 1,2-bis(ethano) bridged bis(cyclopentadienyl) compound, 6,13-diisopropylidenetricyclo[9.3.0(1,11).0(4,8)]tetradeca-1(14),4,7.11-te traene, 5, via a tandem Diels-Alder/retro-Diels-Alder sequence using a 1,5-cyclooctadiyne synthetic equivalent and 6,6-dimethylfulvene is reported. Copyright (C) 1996 Elsevier Science Ltd [References: 28]
机译:一种合成1,2-双(乙醇)桥联双(环戊二烯基)化合物6,13-​​二异丙基亚氨基三环[9.3.0(1,11).0(4,8)] tetradeca-1(14)的新方法,据报道,通过串联的Diels-Alder / retro-Diels-Alder序列使用1,5-环辛二炔合成当量和6,6-二甲基富勒烯,得到4,7.11-te traene,5。版权所有(C)1996 Elsevier Science Ltd [参考:28]

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