A 1,6‐Diphospha‐1,2,4,5‐hexatetraene, Synthesis and Ring Closure Reactions to Cyclobutenes

A 1,6‐Diphospha‐1,2,4,5‐hexatetraene, Synthesis and Ring Closure Reactions to Cyclobutenes
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1,6-Diphospha-1,2,4,5-己四烯,环丁烯的合成和闭环反应

DOI:
10.1002/anie.199009271
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发表时间:
1990
期刊:
影响因子:
--
通讯作者:
K. Polborn
K. Polborn
中科院分区:
--
文献类型:
--
作者:
G. Märkl;P. Kreitmeier;H. Nöth;K. Polborn

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通过锂化丙二烯1的氧化偶联,以几种立体异构形式形成标题化合物2。其中一个在同旋闭环中快速环化得到3,另一个缓慢环化得到4,其通过X射线结构分析表征。芳基= 2,4,6-tBu 3 C 6 H 2。
By oxidative coupling of the lithiated allene 1, the title compound 2 is formed in several stereoisomeric forms. One of them cyclizes rapidly in a conrotatory ring closure to give 3, another cyclizes slowly to give 4, which was characterized by an X‐ray structure analysis. Aryl= 2, 4, 6‐tBu 3 C 6 H 2.