Synthesis of (1,2,3-thiadiazolyl)imidazolidine-2,4-diones by microwave irradiation and characterization of their biological activity / Kalinina T.A., Khamidullina L.A., Shakhmina Y.S., Glukhareva T.V., Kochubei A.A., Cherepanova O.E., Fan Z., Zhu Y., Morzherin Y.Y. // Chemistry of Heterocyclic Compounds. - 2017. - V. , l. . - P. 1-8.

ISSN:

00093122

Type:

Article in Press

Abstract:

[Figure not available: see fulltext.] 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 140°C temperature and microwave irradiation at 170°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. © 2017 Springer Science+Business Media New York

Author keywords:

1,2,3-thiadiazoles; 6-benzylaminopurine; amino acids; gibberellic acid; growth promoters; heterocyclic assemblies; imidazolidine-2,4-diones; microwave synthesis; Pinus sylvestris; seed germination; seed viability; seedling vitality; seedlings; thidiazuron

Index keywords:

нет данных

DOI:

10.1007/s10593-017-1986-z

Смотреть в Scopus:

https://www.scopus.com/inward/record.uri?eid=2-s2.0-85008670825&doi=10.1007%2fs10593-017-1986-z&partnerID=40&md5=c7300dab76960a0a6d985aa4599c554d

Соавторы в МНС:

Другие поля

Поле	Значение
Link	https://www.scopus.com/inward/record.uri?eid=2-s2.0-85008670825&doi=10.1007%2fs10593-017-1986-z&partnerID=40&md5=c7300dab76960a0a6d985aa4599c554d
Affiliations	Ural Federal University named after the First President of Russia B. N. Yeltsin, 19 Mira St., Yekaterinburg, Russian Federation; Botanical Garden of the Urals Branch, Russian Academy of Sciences, 202a 8 Marta St., Yekaterinburg, Russian Federation; State Key Laboratory of Elemento-organic Chemistry, Nankai University, 94 Weijin Rd., Tianjin, China; Joint Innovation Center of Chemical Science and Technology, Nankai University, 94 Weijin Rd., Tianjin, China
Author Keywords	1,2,3-thiadiazoles; 6-benzylaminopurine; amino acids; gibberellic acid; growth promoters; heterocyclic assemblies; imidazolidine-2,4-diones; microwave synthesis; Pinus sylvestris; seed germination; seed viability; seedling vitality; seedlings; thidiazuron
Correspondence Address	Morzherin, Y.Y.; Ural Federal University named after the First President of Russia B. N. Yeltsin, 19 Mira St., Russian Federation; email: yu.yu.morzherin@urfu.ru
Publisher	Springer New York LLC
CODEN	CHCCA
Language of Original Document	English
Abbreviated Source Title	Chem. Heterocycl. Compd.
Source	Scopus