scholarly journals Transition-Metal-Free Highly Efficient Aerobic Oxidation of Sulfides to Sulfoxides under Mild Conditions

Molecules ◽  
2009 ◽  
Vol 15 (1) ◽  
pp. 83-92 ◽  
Author(s):  
Hua Zhang ◽  
Chunyu Chen ◽  
Renhua Liu ◽  
Qiang Xu ◽  
Weiqie Zhao
Keyword(s):  
Transition Metal ◽  
Aerobic Oxidation ◽  
Metal Free ◽  
Mild Conditions ◽  
Oxidation Of Sulfides ◽  
Highly Efficient

DBDMH/NaNO2 Catalyst: Transition-Metal-Free Approach to Highly Efficient Aerobic Oxidation of Sulfides to Sulfoxides

2008 ◽  
Vol 38 (24) ◽  
pp. 4445-4451 ◽  
Author(s):  
Hua Zhang ◽  
Chun-Yu Chen ◽  
Ren-Hua Liu ◽  
Qiang Xu ◽  
Ji-Hong Liu
Keyword(s):  
Transition Metal ◽  
Aerobic Oxidation ◽  
Metal Free ◽  
Oxidation Of Sulfides ◽  
Highly Efficient

Transition-Metal-Free TEMPO Catalyzed Aerobic Oxidation of Alcohols to Carbonyls Using an Efficient Br2Equivalent under Mild Conditions

2013 ◽  
Vol 31 (6) ◽  
pp. 794-798 ◽  
Author(s):  
Jie Zhang ◽  
Zengqiang Jiang ◽  
Dan Zhao ◽  
Guozhen He ◽  
Shuangli Zhou ◽  
...  
Keyword(s):  
Transition Metal ◽  
Aerobic Oxidation ◽  
Metal Free ◽  
Mild Conditions ◽  
Oxidation Of Alcohols

ChemInform Abstract: Transition-Metal-Free TEMPO Catalyzed Aerobic Oxidation of Alcohols to Carbonyls Using an Efficient Br2Equivalent under Mild Conditions.

ChemInform ◽  
2013 ◽  
Vol 44 (46) ◽  
pp. no-no
Author(s):  
Jie Zhang ◽  
Zengqiang Jiang ◽  
Dan Zhao ◽  
Guozhen He ◽  
Shuangli Zhou ◽  
...  
Keyword(s):  
Transition Metal ◽  
Aerobic Oxidation ◽  
Metal Free ◽  
Mild Conditions ◽  
Oxidation Of Alcohols

Transition Metal Free Catalytic Aerobic Oxidation of Methyl-α-d-Glucopyranoside Under Mild Conditions Using Stable Nitroxyl Free Radicals

2012 ◽  
Vol 55 (7-10) ◽  
pp. 556-564 ◽  
Author(s):  
S. K. Tanielyan ◽  
R. L. Augustine ◽  
N. Marin ◽  
G. Alvez ◽  
J. Stapley
Keyword(s):  
Free Radicals ◽  
Transition Metal ◽  
Aerobic Oxidation ◽  
Metal Free ◽  
Mild Conditions

Transition-metal-free Baeyer–Villiger oxidation of benzaldehydes to phenols using Na2S2O8

2019 ◽  
Vol 43 (3-4) ◽  
pp. 115-118
Author(s):  
Wei Li ◽  
Lin-Lin Chen ◽  
Ke Han ◽  
Zhi-Bin Liu ◽  
You-Shun Luan ◽  
...  
Keyword(s):  
Transition Metal ◽  
Practical Approach ◽  
New Approach ◽  
Metal Free ◽  
Mild Conditions ◽  
Highly Efficient ◽  
Operational Simplicity ◽  
Villiger Oxidation

A new approach for preparation of phenols from benzaldehydes using Na2S2O8 has been established. This reaction is a Na2S2O8-promoted Baeyer–Villiger oxidation. It provides a highly efficient and practical approach for the preparation of phenols. The protocol is highlighted by its operational simplicity and mild conditions.

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