School of Chemistry and Molecular Engineering, Institute of Advanced Synthesis, Nanjing Tech University, Nanjing 211816, P. R. China.
Co-Innovation Center for the Sustainable Forestry in Southern China, College of Forestry, Nanjing Forestry University, Nanjing 210037, China.
Org Lett. 2020 Jun 19;22(12):4893-4897. doi: 10.1021/acs.orglett.0c01747. Epub 2020 Jun 4.
A reciprocal-activation strategy for allylic sulfination with unactivated allylic alcohols was developed. In this reaction, the hydrogen bond interaction between allylic alcohols and sulfinic acids allowed for reciprocal activation, which enabled a dehydrative cross-coupling process to occur under mild reaction conditions. This reaction worked in an environmentally friendly manner, yielding water as the only byproduct. A variety of allylic sulfones could be obtained in good to excellent yields with wide functional group tolerance. In gram scale reactions, allylic sulfones could be conveniently isolated in high yield by filtration.
发展了一种用于未活化烯丙醇的烯丙基砜化的相互激活策略。在该反应中,烯丙醇和亚磺酸之间的氢键相互作用允许相互激活,从而使脱水交叉偶联过程能够在温和的反应条件下发生。该反应以环保的方式进行,仅生成水作为唯一的副产物。各种烯丙基砜可以以良好至优异的收率获得,具有广泛的官能团耐受性。在克级反应中,烯丙基砜可以通过过滤方便地以高产率分离。