the National Natural Science Foundation of China(No.21861043);the Yunnan Fundamental Research Projects(No.2019FB016);Scientific and Technological Innovation Team of Optical Functional Materials of Yunnan Provincial Education Department forfinancial support.
Aryl sulfonyl radical triggered cascade cyclization of phenyl-linked 1,6-enynes for the synthesis of biologically important indenes containing alkenyl C—X bonds and 10a,11-dihydro-10H-benzo[b]fluorines is presented.I...
We are grateful to the National Natural Science Foundation of China(Nos.21572196,21871227);the Priority Academic Program Development of Jiangsu Higher Education Institutions(No.BK2013016)for financial support.
A new DBU-catalyzed formal[4+2]cycloaddition between ortho-hydroxyphenyl-substituted para-quinone methides and electron-deficient dienophiles including 3-methyleneoxindoles and 2-aryldeneindene-1,3-diones was establis...
This work was supported by the National Natural Science Foundation of China(21971262,92056201);the National Postdoctoral Program for Innovative Talents(BX20190399);Guangdong Provincial Key Laboratory of Chiral Molecule and Drug Discovery(2019B030301005);the National Mega-project for Innovative Drugs(2019ZX09721001-006-001);the Program for Guangdong Introducing Innovative and Entrepreneurial Teams(2016ZT06Y337);the Fundamental Research Funds for the Central Universities(20ykpy113,18843407).
An unprecedented gold-catalyzed ketene C=O/C=C bifunctionalization method has been developed.Mechanistic studies and density function theory(DFT)calculations indicate that the reaction is initiated by gold-catalyzed W...
We are grateful for the financial support from the National Natural Science Foundation of China (No. 21202154), the Natural Science Foundation of The Jiangsu Higher Education Institutes of China (15KJB150007), the Nanjing Institute of Technology Scientific Research Foundation for Introducing Talents (No. ZKJ201614), and Nanjing Institute of Technology.
The indene moiety is an important unit because of its presence in many chemical catalysts, functional materials and biologically relevant molecules. Herein, we report a facile reaction of arylallenes with benzylic or ...
The three-component reaction of N-phenacylbenzothiazolium bromides, aromatic aldehydes and indane-l,3- dione in ethanol at room temperature in the presence of triethylamine as base afforded functionalized spiro[benzo-...
We are grateful to the National Natural Science Foundation of China (No. 20972048) for the financial support of this work
A base-catalyzed ring-opening of 1-benzylisochromans 1 firstly produced 2-alkenylstilbenes 2, which then underwent a mild acid-catalyzed intramolecular cyclization to furnish 1,2-disubstituted indenes 3 in high yields...
supported by the"100 Talents Program"of the Chinese Academy of Sciences;the National Natural Science Foundation of China(21374025,21372053,and 21102028)
A 54 -electron fullerene acceptor,indene bis-methano[60]fullerene(IBMF),having one indene and two sterically compact CH2 groups was developed.Using P3HT as donor,IBMF solar cells gave a PCE of 5.18%,which is higher th...
The syntheses of three novel substituted indanones namely 2,7 dimethylindan 1 one, 2 methyl 4,7 diethylindan 1 one and 2,4 dimethyl 7 methoxyindan 1 one are described. These indanones were prepared by different routes...