Thionation of amides, 1, 4-diketones, N-(2-oxoalkyl) amides, N, N '-acylhydrazines, and acyl-
protected uridines with the use of a fluorous analogue of the Lawesson's reagent leads to …

A fluorous analogue of Lawesson's reagent for thionation of carbonyl compounds has been
developed and its use demonstrated on a series of amides, esters, and ketones. The …

This review article represents a collection of references explicit to all thionation methods and
related thiocarbonyl derivatives found and described in the literature during the period 1985 …

A simple one-pot reaction between hydroxy-amides (1) located, 1, 3-or 1, 4-to each other,
and Lawesson's reagent (LR) gives sulfur-containg heterocycles such as …

Thionation is the most suitable and efficient method for the synthesis of organosulfur
compounds. Thio-compounds are important intermediates in the synthesis of various …

The most effective catalyst for thionation of cumenes to 4-aryl-1, 2-dithiol-3-thiones, have
been proven to be sym-diphenylguanidine, mercury acetamide, mercaptobenzthiazole+ …

More than 100 years have passed since the first synthesis and structural recognition of
thioamides. Due to the great practical and synthetic applicability of that class of carboxylic …

Iodine-catalyzed thiolation of electron-rich aromatics, including substituted anisole,
thioanisole, phenol, toluene, and naphthalene, using sulfonyl hydrazides as sulfenylation …

Copper (I) trifluoromethanethiolate reacts with a range of diazonium salts containing
electron-withdrawing groups to give the corresponding trifluoromethyl aryl sulfides in high …

The chemical conversion of carbonyl to thiocarbonyl compounds has been an area of
interest to synthetic organic chemists for over a century. The use of phosphorus pentasulfide …