Selective Oxidation of Thioureas in an Ionic Liquid by Employing an Ion-Supported Hypervalent Iodine(III) Reagent.

ChemInform ◽  
2006 ◽  
Vol 37 (4) ◽  
Author(s):  
Weixing Qian ◽  
Erlei Jin ◽  
Weiliang Bao ◽  
Yongmin Zhang
2005 ◽  
Vol 2005 (9) ◽  
pp. 613-616 ◽  
Author(s):  
Weixing Qian ◽  
Erlei Jin ◽  
Weiliang Bao ◽  
Yongmin Zhang

Several 2,4-dialkyl-3,5-bis(arylimino)-1,2,4-thiadiazolidines were synthesised under mild conditions in good yield by the selective oxidation of N-alkyl-N'-arylthioureas by using 1-(4-diacetoxyiodobenzyl)-3-methyl imidazolium tetrafluoroborate [dibmim]+[BF4]- in ionic liquids.


2016 ◽  
Vol 40 (12) ◽  
pp. 10300-10304 ◽  
Author(s):  
Raktani Bikshapathi ◽  
Parvathaneni Sai Prathima ◽  
Vaidya Jayathirtha Rao

An efficient, eco-friendly protocol for selective oxidation of primary and secondary Baylis–Hillman alcohols to the corresponding carbonyl compounds in high yields has been developed with 2-iodosobenzoic acid (IBA).


ChemInform ◽  
2013 ◽  
Vol 45 (1) ◽  
pp. no-no
Author(s):  
Shin A. Moteki ◽  
Asuka Usui ◽  
Tiexin Zhang ◽  
Cesar R. Solorio Alvarado ◽  
Keiji Maruoka

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