C-N Axial Chiral Hypervalent Iodine Reagents: Catalytic Stereoselective α-Oxytosylation of Ketones

被引:15
作者
Alharbi, Haifa [1 ]
Elsherbini, Mohamed [1 ,2 ]
Qurban, Jihan [1 ,3 ]
Wirth, Thomas [1 ]
机构
[1] Cardiff Univ, Sch Chem, Main Bldg,Pk Pl, Cardiff CF10 3AT, Wales
[2] Univ Huddersfield, Dept Chem, Huddersfield HD1 3DH, W Yorkshire, England
[3] Umm Al Qura Univ, Fac Appl Sci, Dept Chem, Mecca, Saudi Arabia
关键词
catalysis; hypervalent iodine; ketones; stereochemistry; α -oxytosylation; ASYMMETRIC-SYNTHESIS; PHENOL DEAROMATIZATION; REARRANGEMENTS; OXIDATION; FLUORINATION; DIAMINATION; SALTS;
D O I
10.1002/chem.202005253
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A simple synthesis of a library of novel C-N axially chiral iodoarenes is achieved in a three-step synthesis from commercially available aniline derivatives. C-N axial chiral iodine reagents are rarely investigated in the hypervalent iodine arena. The potential of the novel chiral iodoarenes as organocatalysts for stereoselective oxidative transformations is assessed using the well explored, but challenging stereoselective alpha-oxytosylation of ketones. All investigated reagents catalyse the stereoselective oxidation of propiophenone to the corresponding chiral alpha-oxytosylated products with good stereochemical control. Using the optimised reaction conditions a wide range of products was obtained in generally good to excellent yields and with good enantioselectivities.
引用
收藏
页码:4317 / 4321
页数:5
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