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Bromination–dehydrobromination route to some naturally occurring 1,6-dioxaspiro[4.4]-nonenes and -nonadienes
Journal of the Chemical Society, Perkin Transactions 1 Pub Date : 1995 , DOI: 10.1039/p19950001309 Yong Qiang Tu , Karl A. Byriel , Colin H. L. Kennard , William Kitching
Journal of the Chemical Society, Perkin Transactions 1 Pub Date : 1995 , DOI: 10.1039/p19950001309 Yong Qiang Tu , Karl A. Byriel , Colin H. L. Kennard , William Kitching
Bromination–dehydrobromination of saturated 1,6-dioxaspiro[4.4]nonanes afforded a variety of naturally occurring 1,6-dioxaspiro[4.4]-nonenes and -nonadienes, such as 2–5 and 8, and can be applied to give unsaturated spirolactones, such as 27.
中文翻译:
溴化-脱氢溴化途径生成一些天然存在的1,6-二氧杂螺[4.4]-壬烯和-壬二烯
饱和1,6-二氧杂螺溴化-脱溴化氢[4.4]壬烷,得到的天然存在的1,6-二氧杂螺各种[4.4] -nonenes和-nonadienes,如2 - 5和8,并且可以应用于以得到不饱和spirolactones如27。
更新日期:2017-01-31
中文翻译:
![](https://scdn.x-mol.com/jcss/images/paperTranslation.png)
溴化-脱氢溴化途径生成一些天然存在的1,6-二氧杂螺[4.4]-壬烯和-壬二烯
饱和1,6-二氧杂螺溴化-脱溴化氢[4.4]壬烷,得到的天然存在的1,6-二氧杂螺各种[4.4] -nonenes和-nonadienes,如2 - 5和8,并且可以应用于以得到不饱和spirolactones如27。