作者:Mariusz Osajda、Jacek Młochowski
DOI:10.1016/s0040-4020(02)00789-5
日期:2002.9
The reactions of 2-(chloroseleno)benzoyl chloride with N, O and S nucleophiles such as alkanols, aminoalkanols, phenols, thiols, aminothiols and thiophenols have been investigated. It was found that the most reactive was a primary amino group which simultaneously underwent selenenylation–acylation. Less reactive hydroxy and thiol groups were selenenylated and/or acylated depending on the structure
已经研究了2-(氯硒代)苯甲酰氯与N,O和S亲核试剂如链烷醇,氨基链烷醇,酚,硫醇,氨基硫醇和硫酚的反应。发现反应性最高的是伯氨基,同时进行亚硒化-酰化。取决于底物的结构和反应条件,较少的反应性羟基和巯基被硒化和/或酰化。