1.
Adv Mater
; 22(42): 4731-5, 2010 Nov 09.
Article
in English
| MEDLINE
| ID: mdl-20734380
2.
Org Lett
; 8(8): 1625-8, 2006 Apr 13.
Article
in English
| MEDLINE
| ID: mdl-16597126
ABSTRACT
[reaction: see text] 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 thioamides, thiophenes, 1,3-thiazoles, 1,3,4-thiadiazoles, and acyl-protected 4-thiouridines. The isolation of the final products in high yields is achieved in most cases by a simple filtration (fluorous solid-phase extraction).