Green synthetic method for 1,5-disubstituted carbohydrazones

Synthetic Communications

Volumn 36, Issue 18, 2006, Pages 2613-2619

  Li, Zheng ^a   Zhu, Wei ^a   Yu, Jinlan ^a   Ma, Xuelin ^a   Lu, Zhong ^a   Xiao, Shuxiu ^a  

^a NORTHWEST NORMAL UNIVERSITY   (China)

Author keywords

Carbohydrazide; Carbohydrazone; Dimethyl carbonate; Solvent free

Indexed keywords

1,5 CARBOHYDRAZONE DERIVATIVE; ALDEHYDE; ALIPHATIC KETONE; CARBOHYDRAZIDE; CARBONIC ACID; HYDRAZINE; METHYL CARBONATE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; INTERMETHOD COMPARISON;

EID: 33748880869     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910600764600     Document Type: Article

References (4)

1. Ono, Y. Catalysis in the production and reactions of dimethyl carbonate, an environmentally benign building block. Appl. Cat., A 1997, 155, 133-166.
2. Kaymakcloglu, B. K.; Rollas, S. Synthesis, characterization and evaluation of antituberculosis activity of some hydrazones. Farmaco 2002, 57, 595-599.
3. Rollas, S.; Gulerman, N.; Erdeniz, H. Synthesis and antimicrobial activity of some new hydrazones of 4-fluorobenzoic acid hydrazide and 3-acetyl-2,5-disubstituted-1,3,4-oxadiazolines. Farmaco 2002, 57, 171-174.
4. Sridhar, S. K.; Pandeya, S. N.; Stables, J. P.; Ramesh, A. Anticonvulsant activity of hydrazones, Schiff and Mannich bases of isatin derivatives. Eur. J. Pharm. Sci. 2002, 16, 129-132.