financially supported by National Key Research and Development Program of China(No.2018YFA0209401);National Natural Science Foundation of China(Nos.22171053,21733003);Natural Science Foundation of Shanghai(No.21ZR1409600)。
Fluoranthenes have attracted tremendous attention due to their unique optoelectronic properties and extensive applications.Although several synthetic methodologies have been developed for the preparation of fluoranthe...
National Natural Science Foundation of China (Nos. 21971092, 21901014, 21472072, 21871018, 21732001 and 21672017);Shenzhen Science and Technology Innovation Committee (No. JCYJ20200109141808025);Characteristic Innovation Project of Guangdong Provincial Education Department (No. 2020KTSCX295) for the financial support。
Pyridinium 1,4-zwitterionic thiolates were applied to a formal [3+2] annulation reaction with modified activated alkynes, affording various tetrasubstituted thiophenes with aryl, alkenyl, alkyl or silyl group at the s...
supported by the National Natural Science Foundation of China(Nos.21871226,21502160,21572194);the Scientific Research Fund of Hunan Provincial Education Department(19B564);the Hunan Provincial Natural Science Foundation of China(No.2020JJ3032);the China Postdoctoral Science Foundation(Nos.2018M632976 and 2019T120709);the Scientific Research Fund of Xiangtan University(No.XDCX2020B110);the Open Fund of Guangdong Provincial Key Laboratory of Lumines-cence from Molecular Aggregates,Guangzhou,510640,China(South China University of Technology,No.2019B030301003).
A convenient synthetic route to 2-heteroaryl-3-hydroxybenzo[b]thiophene derivatives via K_(2)CO_(3)-promoted multicomponent cycliza-tion between o-halogenated benzaldehyde,2-methylquinolines and sulfur powder has been...
We acknowledge the National Natural Science Foundation of China(No.21472136)for financial support.
Main observation and conclusion The reaction of 2-alkynylanisoles/sulfides with SOCl_(2) and DMSO was conducted to conveniently furnish the biologically interesting 3-(methylthio)-benzo[b]furans/thiophenes via intramo...
supported by the National Key Research and Development Program of China(No.2016YFB0401400);the National Natural Science Foundation of China(Nos.21302139,21672120 and 21871158);the Fok Ying Tong Education Foundation of China(No.151014)。
A range of bench-stable carbazole-containing hypervalent iodine(Ⅲ) reagents were synthesized by I-N bond formation in good yields.This kind of benziodoxolone reagents was used for a C-N coupling reaction to introduce...
Supported by the National Natural Science Foundation of China(No.20126008)
Aqueous phase of acids as catalysts for the desulfurization of gasoline by condensation of thiophenes with form- aldehyde in a biphasic system was investigated. Two types of model gasoline with and without aromatics a...
The reaction of the tetrahydrobenzo[b]thiophene derivatives 1a,b with benzoylisothiocyanate (2) afforded the thiourea derivatives 3a,b. Cyclization of the latter products gave the annulated products 4a,b. Compounds 3a...
Project supported by the National Natural Science Foundation of China (No. 20972132).
The polysubstituted thiophene derivatives were conveniently prepared by the four-component reactions of 1,3-thiazolidinedione, aromatic aldehydes, cyanoacetamide and cyclic secondary amines such as pyrrolidine, mor- p...
13C NMR chemical shifts have been calculated for structures of some substituted 3-anilino-2-nitrobenzo- [b]thiophenes (2o) and 2-anilino-3-nitrobenzo[b]thiophenes (3o) derivatives containing OH, NH2, OMe, Me, Et, ...