Daylight LED promotes photochemical ring contraction of 2-amine-4H-pyran-3-carbonitriles with consequent loss of their antifungal activity
-
Published:2021-09-25
Issue:10
Volume:20
Page:1309-1321
-
ISSN:1474-905X
-
Container-title:Photochemical & Photobiological Sciences
-
language:en
-
Short-container-title:Photochem Photobiol Sci
Author:
da Silva Ueveton Pimentel, de Sousa Bianca Lana, Ferreira Bruno Wesley, Barreto Robert Weingart, Amarante Giovanni Wilson, da Silva Rodolfo Rodrigues, Vaz Boniek Gontijo, Varejão Eduardo Vinícius VieiraORCID
Funder
conselho nacional de desenvolvimento científico e tecnológico fundação de amparo à pesquisa do estado de minas gerais
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry
Reference25 articles.
1. Kumar, D., Sharma, P., Singh, H., Nepali, K., Gupta, G. K., Jain, S. K., & Ntie-Kang, F. (2017). The value of pyrans as anticancer scaffolds in medicinal chemistry. RSC Advances, 7, 36977–36999. 2. Verma, A. K., Bishnoi, A., Fatma, S., Srivastava, A., & Singh, V. (2016). A rapid and efficient route to synthesis of 2-amino-4H-pyran-3-carbonitrile derivatives in the presence of L-proline and their antimicrobial activity. Der Pharma Chemica, 8, 380–391. 3. Wang, D.-C., Xie, Y.-M., Fan, C., Yao, S., & Song, H. (2014). Efficient and mild cyclization procedures for the synthesis of novel 2-amino-4H-pyran derivatives with potential antitumor activity. Chinese Chemical Letters, 25, 1011–1013. 4. Rao, N. K., Rao, T. N., Parvatamma, B., Devi, K. P., & Setty, S. C. (2018). Multi component one pot synthesis and characterization of derivatives of 2-amino-7,7-dimethyl-5-oxo-4-phenyl-5,6,7,8-tetrahydro-4H-chromene-3-carbonitrile and study of anti-microbial activity. Bulletin of the Chemical Society of Ethiopia, 32, 133. 5. Bhosle, M. R., Wahul, D. B., Bondle, G. M., Sarkate, A., & Tiwari, S. V. (2018). An efficient multicomponent synthesis and in vitro anticancer activity of dihydropyranochromene and chromenopyrimidine-2,5-diones. Synthetic Communications, 48, 2046–2060.
|
|