Publication Cover
Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 34, 2004 - Issue 12
94
Views
8
CrossRef citations to date
0
Altmetric
Original Articles

Efficient and Novel Synthesis of N‐Aryl‐N′‐ethoxycarbonylthiourea and Arene‐bis‐ethoxycarbonylthiourea Derivatives Catalyzed by TMEDA

, , &
Pages 2205-2213 | Received 12 Dec 2003, Published online: 17 Aug 2006

References

  • Shen , X. , Wen , T. B. , Liu , Q. T. , Huang , X. Y. , Kang , B. S. , Wu , X. L. , Huang , Z. S. and Gu , L. Q. 1997 . Syntheses and crystal structures of copper(I) complexes with alkyl‐thioallophanate derivatives . Polyhedron , 16 : 2605
  • Shen , W. Z. , Fornasieroa , D. and Ralstona , J. 1998 . Effects of collectors, conditioning pH and gases in the separation of sphalerite from pyrite . Miner. Eng. , 11 ( 2 ) : 145 [CROSSREF]
  • Fornasieroa , D. and Ralstona , J. 1997 . Formation of a copper–butyl ethoxycarbonyl thiourea complex . Anal. Chim. Acta , 346 : 237 [CROSSREF] [CSA]
  • Fairthorne , G. , Fornasiero , D. and Ralston , J. 1997 . Interaction of thionocarbamate and thiourea collectors with sulphide minerals: a floatation and adsorption study . Int. J. Miner. Process. , 50 : 227 [CROSSREF] [CSA]
  • Huang , Z. S. , Wu , L. B. , Xiao , J. G. , Huang , Q. P. , Liu , Y. , Gu , L. Q. , Xu , D. H. , Li , B. J. , Weng , G. H. and Ma , K. 1995 . Isolation and structure elucidation of two new urea derivatives from resistant Pyricularia oryzae Cav. rice variety . Youji Huaxue , 15 : 221 (Ch); Chem. Abstr. 1995, 122, 286,681[CSA]
  • Elmoghayar , M. R.H. , Ibrahim , M. K.A. and Darish , F. M. 1984 . Reactions with heterocyclic amines, synthesis of some new azolythiourea derivatives . Org. Prep. Proced. Int. , 16 : 1
  • Wei , T. B. , Chen , J. C. , Wang , X. C. and Zhang , Y. M. 1995 . Transfer catalyzed synthesis of 1‐aryloxyacetyl‐4‐(2‐furoyl) thiosemicarbazide derivatives . J. Chem. Res. (s) , : 138
  • Zhang , Y. M. , Wei , T. B. and Gao , L. M. 2001 . Synthesis and biological activity of N‐Aroyl‐N′‐substituted thiourea derivatives . Synth. Commun. , 31 ( 20 ) : 3099 [CROSSREF]
  • Wei , T. B. , Lin , Q. , Zhang , Y. M. and Wei , W. 2004 . Microwave promoted efficient synthesis of N‐aryl‐N′‐aroyl thioureas under solvent‐free and phase transfer catalysis conditions . Synth. Commun. , 34 ( 1 ) : 175 [CROSSREF]
  • Zhang , Y. M. , Xian , Y. M. and Wei , T. B. 2003 . Chlorobis[N‐ethoxycarbonyl‐N′‐(4‐methylphenyl)thiourea‐κS]copper(I) . Acta Cryst. , C59 : m473
  • Capp , C. W. , Cook , A. H. , Downer , J. D. and Heilbron , S. I. 1948 . Studies in the azole series. Part VIII. The interaction of α‐amino‐nitriles and carbetheoxyisocyanate . J. Chem. Soc. , : 1340 [CROSSREF]
  • Dixon , A. E. and Taylor , J. 1908 . The constitution of “thiocyanates” containing an electronegative group . J. Chem. Soc. , 93 : 684
  • Akira , T. , Hirai , K. and Mastsui , K. 1963 . Studies of the pyrimidine derivatives. XXV. The reaction of alkoxycarbonylthiocyanates and related compounds with the sodium salt of thiamine . Bull. Chem. Soc. Jpn , 36 : 1214
  • Sano , T. , Ohashi , K. and Oriyama , T. 1999 . Remarkably fast acylation of alcohols with benzoyl chloride promoted by TMEDA . Synthesis , : 1141 [CROSSREF]
  • Kunz , H. and Bechtolsheimer , H.‐H. 1982 . 2‐(Triphenylphosphonio)ethoxycarbonyl (Peoc) moiety; an acid stable hydroxy protection group . Synthesis , : 303 (Ger)[CROSSREF]

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.