ChemInform Abstract: OXIDATION OF LONG-CHAIN AND RELATED ALCOHOLS TO CARBONYLS BY DIMETHYL SULFOXIDE ′ACTIVATED′ BY OXALYL CHLORIDE

1978 ◽  
Vol 9 (44) ◽  
Author(s):  
A. J. MANCUSO ◽  
S. L. HUANG ◽  
D. SWERN
Keyword(s):  
Dimethyl Sulfoxide ◽  
Oxalyl Chloride ◽  
Long Chain

Oxidation of long-chain and related alcohols to carbonyls by dimethyl sulfoxide "activated" by oxalyl chloride

1978 ◽  
Vol 43 (12) ◽  
pp. 2480-2482 ◽  
Author(s):  
Anthony J. Mancuso ◽  
Shui-Lung Huang ◽  
Daniel Swern
Keyword(s):  
Dimethyl Sulfoxide ◽  
Oxalyl Chloride ◽  
Long Chain

Dimethyl sulfoxide/oxalyl chloride: A useful reagent for sulfenyletherification

2018 ◽  
Vol 48 (21) ◽  
pp. 2773-2781 ◽  
Author(s):  
Yang Gao ◽  
Siwei Cheng ◽  
Ting Zhang ◽  
Rui Ding ◽  
Yongguo Liu ◽  
...  
Keyword(s):  
Dimethyl Sulfoxide ◽  
Oxalyl Chloride

A Facile Method for the Sulfenyllactonization of Alkenoic Acids Using Dimethyl Sulfoxide Activated by Oxalyl Chloride

Synthesis ◽  
2016 ◽  
Vol 49 (06) ◽  
pp. 1380-1386 ◽  
Author(s):  
Hongyu Tian ◽  
Ting Zhang ◽  
Yifeng Dai ◽  
Siwei Cheng ◽  
Yongguo Liu ◽  
...  
Keyword(s):  
Dimethyl Sulfoxide ◽  
Oxalyl Chloride

The oxysulfenylation of alkenes with dimethyl sulfoxide/oxalyl chloride

2019 ◽  
Vol 49 (20) ◽  
pp. 2662-2670 ◽  
Author(s):  
Yongguo Liu ◽  
Yang Gao ◽  
Zhitong Wang ◽  
Jian Dong ◽  
Rui Ding ◽  
...  
Keyword(s):  
Dimethyl Sulfoxide ◽  
Oxalyl Chloride

Thiomethoxymethylation of 5-Aryloxytetrazoles via Modified Swern Reagents

2005 ◽  
Vol 2005 (3) ◽  
pp. 202-204
Author(s):  
Hossein A. Dabbagh ◽  
Ali Bagheri
Keyword(s):  
Dimethyl Sulfoxide ◽  
Electronic Effect ◽  
Oxalyl Chloride ◽  
Trifluoroacetic Anhydride ◽  
Reaction Conditions ◽  
Swern Oxidation

The modified Swern oxidation of 5-aryloxytetrazole (Ar- = 4-NO2-C6H4-, C6H5-, 2,6-dimethoxy-C6H3-) rings is described using combination of dimethyl sulfoxide with dicyclohexylcarbodiimide (DCC), oxalyl chloride or trifluoroacetic anhydride. The product observed at 1- and/or 2-position of tetrazole rings and yield depends on the substrate, electronic effect of aryloxy group and reaction conditions. It was possible to introduce a thiomethoxymethyl group at 1 and 2-position of tetrazole via rearrangement of Swern intermediate.

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