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Synthesis of N-acylurea derivatives from carboxylic acids and N,N′-dialkyl carbodiimides in water / created by Ali Ramazani, Fatemeh Zeinali Nasrabadi, Aram Rezaei, Morteza Rouhani, Hamideh Ahankar, Pegah Azimzadeh Asiabi, Sang Woo Joo, Katarzyna Ślepokura and Tadeusz Lis

By: Contributor(s): Material type: TextTextSeries: Journal of chemical sciences ; Volume 127, number,12Bangalore : Springer, 2105Content type:
  • text
Media type:
  • unmediated
Carrier type:
  • volume
ISSN:
  • 09743626
Subject(s): LOC classification:
  • QD31 JOU
Online resources: Abstract: Reactions of benzoic acid derivatives and (E)-cinnamic acid derivatives with N , N ′ -dialkyl carbodiimide proceed smoothly at room temperature and in neutral conditions to afford N-acylurea derivatives in high yields. The reaction proceeds smoothly and cleanly under mild conditions and no side reactions were observed. Graphical Abstract Reactions of benzoic acid derivatives and (E)-cinnamic acid derivatives with N,N′-dialkylcarbodiimide proceed smoothly at room temperature and in neutral conditions toafford N-acylurea derivatives in high yields, and no side reactions were observed.
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Item type Current library Call number Vol info Status Notes Date due Barcode
Journal Article Journal Article Main Library - Special Collections QD31 JOU (Browse shelf(Opens below)) Vol. 127, no.12 (pages 2269-2282) Not for loan For in house use only

Reactions of benzoic acid derivatives and (E)-cinnamic acid derivatives with N , N ′ -dialkyl carbodiimide proceed smoothly at room temperature and in neutral conditions to afford N-acylurea derivatives in high yields. The reaction proceeds smoothly and cleanly under mild conditions and no side reactions were observed. Graphical Abstract Reactions of benzoic acid derivatives and (E)-cinnamic acid derivatives with N,N′-dialkylcarbodiimide proceed smoothly at room temperature and in neutral conditions toafford N-acylurea derivatives in high yields, and no side reactions were observed.

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