Oxidation coupling of organic thiols to disulphides with Tetramethylammonium
Fluorochromate(VI) (TMAFC)

Hosein Imanieh; Shahriar Ghamami; Mohammad Mohammadi

doi:10.3390/ecsoc-10-01373

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Contribution to synthesis of some glucopyranosylamines containing 1,3-thiazole and 1,3-benzothiazole rings from 4,6-O-ethylidene-Dglucopyranose

Oxidation coupling of organic thiols to disulphides with Tetramethylammonium Fluorochromate(VI) (TMAFC)

Hosein Imanieh

¹,

Shahriar Ghamami

¹,

Mohammad kazem Mohammadi

^{*

2}

¹ Department of Chemistry, Faculty of Science, Imam Khomeini International University Qazvin, Iran.P.O.Box:288
² Department of Chemistry, Cslamic Azad University of Firouzabad, Firouzabad, Iran, Postal Code: 74715D

Published: 30 November 2006 by MDPI in The 10th International Electronic Conference on Synthetic Organic Chemistry session General Organic Synthesis

https://doi.org/10.3390/ecsoc-10-01373

Abstract: Tetramethylammonium Fluorochromate has been found to oxidize alcohols to corresponding aldehydes and ketones. Without polymerization of double bonds, over oxidation and other side reactions. This reagent has been found that effective for oxidation of thiols to disulphides.

Keywords: Tetramethylammoniumfluorochromate(VI), Thiols, Oxidation

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Hosein Imanieh

Shahriar Ghamami

Mohammad Mohammadi