Preparation and Some Reactions of Thiobis-N-(trifluoromethyl) amines1
TE STEVENS
Index: Stevens,T.E. Journal of Organic Chemistry, 1961 , vol. 26, p. 3451 - 3457
Full Text: HTML
Citation Number: 3
Abstract
The fluorination of aryl and alkyl isothiocyanates with iodine pentafluoride in pyridine solution has been found to produce thiobis-N-substituted iV-(trifluoromethy1) amines. The preparation and some of the reactions of these novel compounds are discussed. A unique rearrangement of a thioi) isaniinc to a diphenyl sulfide is reported.
Related Articles:
Variation of xantphos-based ligands in the palladium-catalyzed reaction of aryl halides with ureas
[Sergeev; Artamkina; Beletskaya Russian Journal of Organic Chemistry, 2003 , vol. 39, # 12 p. 1741 - 1752]
[Tsuji, Yasushi; Takeuchi, Ryo; Watanabe, Yoshihisa Journal of Organometallic Chemistry, 1985 , vol. 290, p. 249 - 256]
Palladium-catalyzed reaction of aryl halides with ureas
[Artamkina, Galina A.; Sergeev, Alexey G.; Beletskaya, Irina P. Tetrahedron Letters, 2001 , vol. 42, # 26 p. 4381 - 4384]
Catalytic oxidative carbonylation of arylamines to ureas with W (CO) 6/I2 as catalyst
[Zhang, Li; Darko, Ampofo K.; Johns, Jennifer I.; McElwee-White, Lisa European Journal of Organic Chemistry, 2011 , # 31 p. 6261 - 6268]
Palladium-catalyzed arylation of ureas
[Artamkina; Sergeev; Beletskaya Russian Journal of Organic Chemistry, 2002 , vol. 38, # 4 p. 538 - 545]