supported by the National Natural Science Foundation of China(22001065);the Science and Technology Foundation of Hunan Province(2021JJ30090);Guangdong Provincial Key Laboratory of Catalysis(2020B121201002);Shenzhen Science and Technology Program(KQTD20210811090112004);supported by Center for Computational Science and Engineering at SUSTech;the CHEM high-performance supercomputer cluster(CHEM-HPC)located at the Department of Chemistry,SUSTech。
The conversion of commercially available chiral sulfinamides into pharmaceutically useful chiral sulfoximines via direct SIVfunctionalization is synthetically attractive but challenging due to the competitive reaction...
financially supported by the Shandong Provincial Natural Science Foundation(Nos.ZR2021JQ16,ZR2019YQ19and ZR2019BEM018);the Project of Shandong Province Higher Educational Science and Technology Program(No.2019KJA026);the National Natural Science Foundation of China(Nos.51403113 and 52072193);the Shandong Provincial College Students'Innovative Entrepreneurial Training(No.S202111065214).
Aromatic carbonyls have evoked sustained attention in the field of room-temperature phosphorescence(RTP).The introduction of carbonyl groups is a general way to achieve RTP for their effective intersystem crossing(ISC...
supported by the National Natural Science Foundation of China(No.22161039);the Excellent Young Teachers Plan of Bingtuan(2017CB001 and CZ027203,CZ002203);the International Cooperation Project of Shihezi University(No.GJHZ201801).
A facile and transition-metal-free method for the synthesis of 4-amino isoquinolin-1(2H)-ones has beendeveloped. Arynes react with 4,5-disubstituted oxazoles through a tandem Diels–Alder reaction/dehydrogenation–aro...
the financial support from the National Natural Science Foundation of China(No.21772134);the Fundamental Research Funds for the Central Universities(No.20826041D4117)。
An efficient Pd-catalyzed double annulation reaction of 1-(2,6-dibro mophenyl)-1 H-pyrroles with arynes is developed to synthesizeπ-extended dibenzo[d,k]ullazines in good to excellent yields.For the first time,the pa...
the National Natural Science Foundation of China(Nos.21572002,21272005);The Research Culture Funds of Anhui Normal University;Department of Human Resources of Anhui Province for financial support。
This study presents a facile strategy for the formation of highly substituted butterfly 1,4-adducts/9,10-adducts via the Diels-Alder reaction of benzyne intermediates.The method achieves very good to excellent yields ...
the National Natural Science Foundation of China(No.21162022);the Team Innovation Project of Shihezi University(No.2011ZRKETD-04) for financial support
A cascade insertion-nucleophilic annulation reaction of salicyl N-tosylimines with aryne generated in situ from 2-(trimethyl- silyl) aryl triflate and KF-18-crown-6 has been developed, providing 9-aminoxanthenes eff...
We are grateful to the National Natural Science Foundation of China (Nos. 20332060 and 2472072)
One novel carbon-carbon bond insertion reaction of arynes has been developed. By this reaction β-keto sulfones can insert the triple bond of arynes to prepare polysubstituted ortho-keto benzyl sulfones.