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首页> 外文期刊>Synlett >Synthesis of highly functionalized 1,3-oxathioles via an unusual [4+1] annulation of α,α'-dioxothione with 1,2-diaza-1,3-dienes
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Synthesis of highly functionalized 1,3-oxathioles via an unusual [4+1] annulation of α,α'-dioxothione with 1,2-diaza-1,3-dienes

机译:通过异常的α,α'-二氧噻吩与[1,2-二氮杂-1,3-二烯]的[4 + 1]环化反应合成高度官能化的1,3-氧杂硫醇

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摘要

The present method provides highly functionalized 1,3-oxathioles through an unusual base-promoted [4+1] annulation between α,α'-dioxothione, generated in situ from a phthalimide precursor, and 1,2-diaza-1,3-dienes. An intriguing scaffold comprised of spiro-fused oxathiole and pyrazolone components was also obtained in moderate yield.
机译:本方法通过由邻苯二甲酰亚胺前体原位生成的α,α'-二氧噻吩与1,2-二氮杂1,3-之间的异常碱促进的[4 + 1]环化提供了高度官能化的1,3-氧杂硫醇。二烯。还以中等收率获得了由螺-融合的草硫醇和吡唑啉酮组分组成的有趣支架。

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