Efficient Oxidation of Alcohols to Carbonyl Compounds byN,N-Dichloro-4-Methylbenzenesulfonamide under Mild Conditions

2007 ◽  
Vol 54 (2) ◽  
pp. 465-468 ◽  
Author(s):  
Ardeshir Khazaei ◽  
Ayeh Raiatzadeh ◽  
Amin Rostami
Synthesis ◽  
2020 ◽  
Author(s):  
Jia-Jia Zhao ◽  
Hong-Hao Zhang ◽  
Shouyun Yu

Visible light photoredox catalysis has recently emerged as a powerful tool for the development of new and valuable chemical transformations under mild conditions. Visible-light promoted enantioselective radical transformations of imines and iminium intermediates provide new opportunities for the asymmetric synthesis of amines and asymmetric β-functionalization of unsaturated carbonyl compounds. In this review, the advance in the catalytic asymmetric radical functionalization of imines, as well as iminium intermediates, are summarized. 1 Introduction 2 The enantioselective radical functionalization of imines 2.1 Asymmetric reduction 2.2 Asymmetric cyclization 2.3 Asymmetric addition 2.4 Asymmetric radical coupling 3 The enantioselective radical functionalization of iminium ions 3.1 Asymmetric radical alkylation 3.2 Asymmetric radical acylation 4 Conclusion


Tetrahedron ◽  
2003 ◽  
Vol 59 (35) ◽  
pp. 6739-6750 ◽  
Author(s):  
Jun-ichi Matsuo ◽  
Daisuke Iida ◽  
Hiroyuki Yamanaka ◽  
Teruaki Mukaiyama

2000 ◽  
Vol 65 (7) ◽  
pp. 1915-1918 ◽  
Author(s):  
Waldemar Adam ◽  
Feyissa Gadissa Gelalcha ◽  
Chantu R. Saha-Möller ◽  
Veit R. Stegmann

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