Department of Chemistry, Huaibei Normal University , Huaibei, Anhui 235000, P. R. China.
Org Lett. 2015 Feb 20;17(4):832-5. doi: 10.1021/ol503659t. Epub 2015 Feb 2.
A novel and efficient electrophilic sulfenylation of indoles with arylsulfinic acids is realized. The reaction utilizes readily available starting materials in water under catalyst- and additive-free conditions, providing an alternative and attractive approach to 3-arylsulfinylindoles with high yields. Preliminary mechanistic investigation suggested that the reaction is through an electrophilic substitution process.
实现了吲哚与芳基亚砜的新型高效亲电亚磺酰化反应。该反应在无催化剂和添加剂的条件下,以水为溶剂,利用易得的起始原料,以高产率得到 3-芳基亚磺酰基吲哚,为其提供了一种替代的、有吸引力的方法。初步的机理研究表明,该反应是通过亲电取代过程进行的。