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1,6-Conjugate addition initiated formal [4+2] annulation of p-quinone methides with sulfonyl allenols: a unique access to spiro[5.5]undeca-1,4-dien-3-one scaffolds.
Chemical Communications ( IF 4.9 ) Pub Date : 2020-04-03 , DOI: 10.1039/d0cc01005g Ganesh S Ghotekar 1 , Sachin R Shirsath , Aslam C Shaikh , M Muthukrishnan
Chemical Communications ( IF 4.9 ) Pub Date : 2020-04-03 , DOI: 10.1039/d0cc01005g Ganesh S Ghotekar 1 , Sachin R Shirsath , Aslam C Shaikh , M Muthukrishnan
Affiliation
An expedient one-pot synthesis of carbocyclic spiro[5.5]undeca-1,4-dien-3-ones via 1,6-conjugate addition initiated formal [4+2] annulation sequences by employing p-quinone methides and sulfonyl allenols is presented. Furthermore, this synthetic protocol tolerates a wide variety of p-quinone methides and sulfonyl allenols and affords the corresponding structurally unique spiro[5.5]undeca-1,4-dien-3-ones in good yield under mild reaction conditions.
中文翻译:
1,6-缀合物的添加引发了对苯醌甲基化物与磺酰基烯丙醇的正式[4 + 2]环空:螺旋[5.5] undeca-1,4-dien-3-one支架的独特获得。
提出了一种方便的一锅合成碳环螺[5.5] undeca-1,4-dien-3-one的方法,方法是通过对醌甲基化物和磺酰基烯丙醇通过1,6-缀合物加成引发的正式[4 + 2]环化序列进行。此外,该合成方案可耐受多种对醌甲基化物和磺酰基烯丙醇,并在温和的反应条件下以良好的收率提供相应的结构独特的螺[5.5] undeca-1,4-二烯-3-酮。
更新日期:2020-03-24
中文翻译:
1,6-缀合物的添加引发了对苯醌甲基化物与磺酰基烯丙醇的正式[4 + 2]环空:螺旋[5.5] undeca-1,4-dien-3-one支架的独特获得。
提出了一种方便的一锅合成碳环螺[5.5] undeca-1,4-dien-3-one的方法,方法是通过对醌甲基化物和磺酰基烯丙醇通过1,6-缀合物加成引发的正式[4 + 2]环化序列进行。此外,该合成方案可耐受多种对醌甲基化物和磺酰基烯丙醇,并在温和的反应条件下以良好的收率提供相应的结构独特的螺[5.5] undeca-1,4-二烯-3-酮。