219815-16-4Relevant articles and documents
Concentrated solar radiation as a renewable heat source for a preparative-scale and solvent-free Biginelli reaction
Gadkari, Yatin U.,Hatvate, Navnath T.,Takale, Balaram S.,Telvekar, Vikas N.
supporting information, p. 8167 - 8170 (2020/06/09)
A well-known Biginelli reaction for the synthesis of 3,4-dihydropyrimidin-2(1H)-ones/thiones was performed in an environmentally responsible manner. Large numbers of substrates were screened, and found to give excellent yields of the desired products. In
UV-Light-Irradiated Trifluoromethylation of Diheteroaryl Disulfides with CF3SO2Na
Cao, Bao-Qian,Qiu, Yi-Feng,Zhang, Xi,Zhu, Zheng-He,Quan, Zheng-Jun,Wang, Xi-Cun
supporting information, p. 1208 - 1214 (2019/02/07)
A simple protocol for the UV light irradiated preparation of heteroaryl trifluoromethyl thioethers from disulfides and inexpensive, environmentally sodium triflinate (CF3SO2Na) has been developed. The features of simple and clean rea
An efficient synthesis of biopertinent dihydropyrimidine (thi) one derivatives via three-component one-pot synthesis catalyzed by tetrachlorosilane
Khatab,El-Bayouki,Basyouni,Sroor
, p. 291 - 305 (2015/10/20)
SERIES of dihydropyrimidine(thi)one derivatives were prepared, in good yields at room temperature by using a modified Biginelli reaction. The products were obtained through a one-pot three-component coupling of β-diketones, aldehydes and urea (or thiourea
