Metal-Free Deoxygenation of Amine N-Oxides: Synthetic and Mechanistic Studies

被引:3
|
作者
Lecroq, William [1 ]
Schleinitz, Jules [2 ]
Billoue, Mallaury [1 ]
Perfetto, Anna [3 ]
Gaumont, Annie-Claude [1 ]
Lalevee, Jacques [4 ]
Ciofini, Ilaria [3 ]
Grimaud, Laurence [2 ]
Lakhdar, Sami [5 ]
机构
[1] Normandie Univ, LCMT, ENSICAEN, UNICAEN,CNRS, 6 Blvd Marechal Juin, F-14000 Caen, France
[2] PSL Univ, Sorbonne Univ, Lab Biomol, LBM,Dept Chim,Ecole Normale Super,CNRS, F-75005 Paris, France
[3] PSL Univ, Inst Chem Life & Hlth Sci I CLeHS, Chim ParisTech, CNRS, 11 Rue P&M Curie, F-75005 Paris, France
[4] Univ Haute Alsace, CNRS, UMR 7361, IS2 M, F-68100 Mulhouse, France
[5] Univ Paul Sabatier, Lab Heterochim Fondamentale & Appl LHFA, UMR 5069, 118 Route Narbonne, F-31062 Toulouse 09, France
基金
欧洲研究理事会;
关键词
deoxygenation; mechanisms; photochemistry; organocatalysis; selectivity; DENSITY-FUNCTIONAL METHODS; ALKYLATION; SULFOXIDES; REDUCTION; ENERGIES; ESTERS;
D O I
10.1002/cphc.202100108
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We report herein an unprecedented combination of light and P(III)/P(V) redox cycling for the efficient deoxygenation of aromatic amine N-oxides. Moreover, we discovered that a large variety of aliphatic amine N-oxides can easily be deoxygenated by using only phenylsilane. These practically simple approaches proceed well under metal-free conditions, tolerate many functionalities and are highly chemoselective. Combined experimental and computational studies enabled a deep understanding of factors controlling the reactivity of both aromatic and aliphatic amine N-oxides.
引用
收藏
页码:1237 / 1242
页数:6
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