A Versatile and Highly Selective Hypervalent Iodine (III)/2,2,6,6-Tetramethyl-1-piperidinyloxyl-Mediated Oxidation of Alcohols to Carbonyl Compounds

1997 ◽  
Vol 62 (20) ◽  
pp. 6974-6977 ◽  
Author(s):  
Antonella De Mico ◽  
Roberto Margarita ◽  
Luca Parlanti ◽  
Andrea Vescovi ◽  
Giovanni Piancatelli
2009 ◽  
pp. 2086 ◽  
Author(s):  
Muhammet Uyanik ◽  
Kazuaki Ishihara

2013 ◽  
Vol 9 ◽  
pp. 1437-1442 ◽  
Author(s):  
Nida Ambreen ◽  
Ravi Kumar ◽  
Thomas Wirth

Hypervalent iodine(III)/TEMPO-mediated oxidation of various aliphatic, aromatic and allylic alcohols to their corresponding carbonyl compounds was successfully achieved by using microreactor technology. This method can be used as an alternative for the oxidation of various alcohols achieving excellent yields and selectivities in significantly shortened reaction times.


RSC Advances ◽  
2018 ◽  
Vol 8 (56) ◽  
pp. 32055-32062 ◽  
Author(s):  
Ajay H. Bansode ◽  
Gurunath Suryavanshi

A highly efficient, metal free rapid protocol studied mechanistically the oxidation of primary and secondary amines to their corresponding carbonyl compounds using PhI(OAc)2and catalytic TEMPO to provide diverse products in excellent yields.


2010 ◽  
Vol 88 (4) ◽  
pp. 362-366 ◽  
Author(s):  
Chenjie Zhu ◽  
Lei Ji ◽  
Qian Zhang ◽  
Yunyang Wei

An efficient, facile, and mild oxidation of alcohols to the corresponding carbonyl compounds with m-chloroperbenzoic acid (mCPBA) and N-hydroxyphthalimide (NHPI) in the presence of a catalytic amount of iodobenzene was reported. The oxidation proceeded in mixed solvent at room temperature to afford carbonyl compounds in excellent yields. A possible mechanism for the oxidation was proposed.


ChemInform ◽  
2009 ◽  
Vol 40 (32) ◽  
Author(s):  
Muhammet Uyanik ◽  
Kazuaki Ishihara

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