YM Ren, C Cai, RC Yang - RSC advances, 2013 - pubs.rsc.org
The multicomponent reactions (MCRs) consist of two or more synthetic steps which are carried out without isolation of any intermediate thus reducing time, saving money, energy …
RG Puligoundla, S Karnakanti, R Bantu, K Nagaiah… - Tetrahedron …, 2013 - Elsevier
A wide variety of quinazolinone derivatives have been synthesized by condensation of 3- amino-1, 2, 4-triazole and 2-aminobenzimidazole as amine sources, with aromatic …
Z Zeng, H Jin, X Song, Q Wang, M Rudolph… - Chemical …, 2017 - pubs.rsc.org
Gold-catalyzed regioselective cyclocarboamination of ynamides with 1, 3, 5-triazinanes opens a facile and modular access to valuable 5-aminotetrahydropyrimidines in good to …
VV Dotsenko, KA Frolov, EA Chigorina… - Russian chemical …, 2019 - Springer
The review summarizes the results obtained by our research group over the past 15 years in chemistry of N-, S, N-, and Se, N-heterocycles resulted from aminomethlation of a wide …
VV Dotsenko, AV Bespalov, AS Vashurin… - ACS …, 2021 - ACS Publications
trans-2-Amino-4-aryl-5-benzoyl-4, 5-dihydrothiophene-3-carbonitriles were prepared either by the reaction of 3-aryl-2-cyanothioacrylamides with α-thiocyanatoacetophenone or by the …
ВВ Доценко, КА Фролов, ЕА Чигорина… - … Академии наук. Серия …, 2019 - elibrary.ru
В обзоре представлены результаты работы авторского коллектива за последние 15 лет в области химии N-, S, N-и Se, N-гетероциклических систем, получаемых …
AA Amiri, S Javanshir, Z Dolatkhah, SMJ Nabavi - sid.ir
Pyrimidines and their analogues hold a special place among pharmaceutically significant natural products and synthetic compounds [1]. Tetrahydropyrimidine scaffold has displayed …
In chapter 2, a novel and atom-economical synthesis of fully substituted 4-aminoimidazoles via gold-catalyzed selective [3+ 2] annulation of 1, 2, 4-oxadiazoles with ynamides is …
P Rairala, B Yadagiri, R Bantu… - Letters in Organic …, 2015 - ingentaconnect.com
PEG-400 was found to be an inexpensive, non-toxic and eco-friendly reaction medium for synthesis of pyramido [2, 1-b] benzothiazole derivatives. Utilizing this protocol, we are …