Organocatalytic oxidation of substituted anilines to azoxybenzenes and nitro compounds: mechanistic studies excluding the involvement of a dioxirane intermediate

2017 ◽  
Vol 19 (5) ◽  
pp. 1291-1298 ◽  
Author(s):  
Errika Voutyritsa ◽  
Alexis Theodorou ◽  
Maroula G. Kokotou ◽  
Christoforos G. Kokotos

Organocatalytic and environmentally friendly approaches for the selective oxidation of substituted anilines either to azoxybenzenes or to nitro compounds were developed.

2013 ◽  
Vol 42 (13) ◽  
pp. 4725 ◽  
Author(s):  
Debabrata Chatterjee ◽  
Sabine Rothbart ◽  
Rudi van Eldik

2013 ◽  
Vol 9 ◽  
pp. 602-607 ◽  
Author(s):  
Lennart Möhlmann ◽  
Stefan Ludwig ◽  
Siegfried Blechert

This publication describes a highly selective oxidation of aldehydes to the corresponding acids or esters. The reaction proceeds under metal-free conditions by using N-heterocyclic carbenes as organocatalysts in combination with environmentally friendly oxygen as the terminal oxidation agent.


ChemInform ◽  
2010 ◽  
Vol 27 (34) ◽  
pp. no-no
Author(s):  
R. BALLINI ◽  
F. PAPA ◽  
P. BOVICELLI

ACS Omega ◽  
2019 ◽  
Vol 4 (5) ◽  
pp. 9453-9457 ◽  
Author(s):  
Krishnan Ravi ◽  
Balasaheb D. Bankar ◽  
Sana Jindani ◽  
Ankush V. Biradar

RSC Advances ◽  
2017 ◽  
Vol 7 (89) ◽  
pp. 56764-56770 ◽  
Author(s):  
Pipattra Mayurachayakul ◽  
Wanchai Pluempanupat ◽  
Choladda Srisuwannaket ◽  
Oraphin Chantarasriwong

A convenient and environmentally friendly procedure for the synthesis of polyhydroquinolines via a one-pot four-component reaction has been developed. A detailed mechanistic study of the reaction is presented.


2003 ◽  
Vol 75 (2-3) ◽  
pp. 265-272 ◽  
Author(s):  
R. Saladino ◽  
E. Mincione ◽  
O. A. Attanasi ◽  
Paolino Filippone

A convenient and efficient application of microencapsulated/methylrhenium trioxide (MTO) and MTO/pyridine systems for the selective oxidation of cardanol derivatives is reported. Environmentally friendly and low-cost H2O2 was used as the oxygen atom donor. The catalysts were stable systems for at least five recycling experiments. In the oxidation of C2 alkyl-substituted cardanol derivatives, high conversion and yields of the corresponding para-benzoquinones were obtained. By contrast, in the absence of the C2 substituent, an unprecedented oxidative degradation to di-γ-lactone derivative was observed.


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