吡咯烷
废止
化学
激进的
催化作用
基质(水族馆)
区域选择性
药物化学
Atom(片上系统)
组合化学
范围(计算机科学)
硫黄
有机化学
海洋学
地质学
嵌入式系统
计算机科学
程序设计语言
作者
Jing Yang,Yan Gu,Xiao‐Qi Yu,Xiaoqing Lv,Bo Liu,Yun Liu,Liangce Rong
标识
DOI:10.1002/slct.202300307
摘要
Abstract An energy economical and radical‐involved regioselective difunctionalization annulation of 1,6‐enynes with thiosulfonates or selenosulfonates accessing to pyrrolidine derivatives has been developed. The catalytic amount of TBHP was sufficient to initiate and enable the simultaneous formation of a C(sp 3 )−S(O 2 Ar) bond and a C(sp 2 )−S(Ar) or C(sp 2 )−Se(Ph) bond across the C=C and C≡C bond of 1,6‐enynes by utilizing two different sulphur radicals. The reaction shows broad substrate scope, moderate to good yields, and 100 % atom economy.
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