Synthesis of (1,2,3-thiadiazolyl)imidazolidine-2,4-diones by microwave irradiation and characterization of their biological activity / Kalinina Tatiana A.,Khamidullina Liliya A.,Shakhmina Yulia S.,Glukhareva Tatiana V.,Kochubei Alena A.,Cherepanova Olga E.,Fan Zhijin,Zhu Yujie,Morzherin Yuri Yu. // CHEMISTRY OF HETEROCYCLIC COMPOUNDS. - 2016. - V. 52, l. 11. - P. 910-917.

ISSN/EISSN:

0009-3122 / 1573-8353

Type:

Article

Abstract:

The effects of microwave irradiation on the synthesis of (1,2,3-thiadiazol-4-yl)- and (1,2,3-thiadiazol-5-yl)imidazolidine-2,4-diones by cyclocondensation of the respective (1,2,3-thiadiazolyl)ureidoacetic acids were studied. The reactions were studied under the conditions of traditional heating at 140A degrees C temperature and microwave irradiation at 170A degrees C. It was shown that microwave heating of (1,2,3-thiadiazol-5-yl)ureido derivatives of carboxylic acids led to the formation of imidazolidine ring, unlike in the case of (1,2,3-thiadiazol-4-yl)ureido derivatives, for which traditional heating was more effective. The derivatives of (1,2,3-thiadiazolyl)imidazolidine-2,4-diones and (1,2,3-thiadiazolyl)ureidoacetic acids were studied with regard to their effects on pine seed germination and seedling growth.

Author keywords:

amino acids; 6-benzylaminopurine; gibberellic acid; imidazolidine-2,4-diones; 1,2,3-thiadiazoles; thidiazuron; growth promoters; heterocyclic assemblies; microwave synthesis; seed germination; seed vi HERBICIDAL ACTIVITY; ACID; ESTERS

DOI:

10.1007/s10593-017-1986-z

Web of Science ID:

ISI:000392938800008

Соавторы в МНС:

Другие поля

Поле	Значение
Month	NOV
Publisher	SPRINGER
Address	233 SPRING ST, NEW YORK, NY 10013 USA
Language	English
EISSN	1573-8353
Keywords-Plus	HERBICIDAL ACTIVITY; ACID; ESTERS
Research-Areas	Chemistry
Web-of-Science-Categories	Chemistry, Organic
Author-Email	common@botgard.uran.ru fanzj@nankai.edu.cn zhuyujie@mail.nankai.edu.cn yu.yu.morzherin@urfu.ru
Funding-Acknowledgement	Ministry of Education and Science of the Russian Federation {[}4.560.2014-K]; Russian Foundation for Basic Research {[}mol\_a16-33-00556]; Presidium of Russian Academy of Sciences {[}15-12-4-13]; National Natural Science Foundation of China {[}21372132]; International Science \& Technology Cooperation Program of China {[}2014DFR41030]; Tianjin Natural Science Foundation {[}14JCYBJC20400]
Funding-Text	The results were obtained within the framework of State Assignment No. 4.560.2014-K with the Ministry of Education and Science of the Russian Federation and with support from the Russian Foundation for Basic Research (grant mol\_a16-33-00556) and the Complex program No. 15-12-4-13 of the Presidium of Russian Academy of Sciences.; Professor Zhijin Fan acknowledges financial support from the National Natural Science Foundation of China (No. 21372132), the International Science \& Technology Cooperation Program of China (No. 2014DFR41030), and Tianjin Natural Science Foundation (No. 14JCYBJC20400).
Number-of-Cited-References	40
Usage-Count-Last-180-days	2
Usage-Count-Since-2013	2
Journal-ISO	Chem. Heterocycl. Compds.
Doc-Delivery-Number	EJ0ZC