[2.2]Paracyclophane-based coumarins: effective organo-photocatalysts for light-induced desulfonylation processes

被引:3
作者
Brom, Jules [1 ]
Maruani, Antoine [1 ]
Turcaud, Serge [1 ]
Lajnef, Sonia [1 ]
Peyrot, Fabienne [1 ,2 ]
Micouin, Laurent [1 ]
Benedetti, Erica [1 ]
机构
[1] Univ Paris Cite, CNRS, Lab Chim & Biochim Pharmacol & Toxicol, F-75006 Paris, France
[2] Sorbonne Univ, Inst Natl Super Professorat & Educ INSPE, Acad Paris, F-75016 Paris, France
关键词
MACRO RINGS; CLEAVAGE; CONSEQUENCES; SULFONAMIDES; DEPROTECTION; ARYLATION; AMIDES; BOND;
D O I
10.1039/d3ob01711g
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Herein, we demonstrate for the first time that coumarins derived from [2.2]paracyclophane (pCp) can act as effective organo-photocatalysts and promote the reductive cleavage of sulfonamides under light-irradiation. In the presence of these original compounds, photodesulfonylation reactions occur under mild conditions at low catalyst loadings in the presence of Hantzsch ester. Theoretical and experimental investigations are described, which elucidate the reaction mechanism and the nature of the active species involved in the photocatalytic process. This proof-of-concept study paves the way for further application of pCps in the field of photocatalysis. An unprecedented photocatalytic activity of coumarins derived from [2.2]paracyclophane is disclosed, which allows the reductive photocleavage of various sulfonamides under mild conditions.
引用
收藏
页码:59 / 64
页数:6
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