We are grateful to the National Natural Science Foundation of China(Nos.21961037,21861036,22161044 and 22201241);the Program for Tianshan Innovative Research Team of Xinjiang Uygur Autonomous Region(No.2021D14011);the Natural Science Foundation of Xinjiang Uygur Autonomous Region(Nos.2020D01C077 and 2021D01E10);the Key Program of Natural Science Foundation of Xinjiang Uygur Autonomous Region(No.2022D01D06)for support of this research。
Herein,we achieved a green and efficient dearomatization for the synthesis of 2,3-functionalized polycyclic indolines in an electrochemical way.This avoiding of external oxidants and metals approach allowed various nu...
supported by the National Natural Science Foundation of China(22071253,21831008);the Beijing National Laboratory for Molecular Sciences(BNLMS-CXXM-202003)。
The cooperative visible-light mediated and NHC-catalyzed dearomative arylation-acylation of N-(2-bromobenzoyl)indoles with aldehydes was developed, affording the corresponding highly functionalized polycyclic indoline...
supported by the National Natural Science Foundation of China(22171186,22222107);ShanghaiTech University Start-up Funding;Analytical Instrumentation Center(#SPSTAIC10112914),SPST,ShanghaiTech University。
A novel kinetic resolution(KR) method has been developed for 3,3-disubstituted indolines, whose catalytic asymmetric synthesis remains a significant challenge in organic synthesis. The key to the success of this KR pr...
financial support from the National Natural Science Foundation of China(Nos.22125108,22101238,92056104 and 21772161);the China Postdoctoral Science Foundation(No.2020M680087);the Natural Science Foundation of Fujian Province of China(No.2019J02001);the President Research Funds from Xiamen University(No.20720210002);the Fundamental Research Funds for the Central Universities(No.20720202008);NFFTBS(No.J1310024)。
Catalytic asymmetric dearomatization of indoles and alkynes has received much attention in the past decade because this strategy offers an attractive and alternative way for the efficient synthesis of valuable chiral ...
The financial support was provided by the National Natural Science Foundation of China(no.22001181 and 22077090);the Sichuan Science and Technology Program(2021YJ0407).
A highly efficient dearomatization of 3-(2-isocyanoethyl)indoles with in situ generated nitrile imines has been developed through a nucleophilic/Friedel–Crafts/aza-Mannich type cascade and 1,3-dipolar cyclo-addition ...
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...
the Shanghai Institute of Materia Medica;the Chinese Academy of Sciences;the National Natural Science Foundation of China(Nos.21772211 and 21920102003);the Youth Innovation Promotion Association CAS(Nos.2014229 and 2018293);the Science and Technology Commission of Shanghai Municipality(Nos.17JC1405000 and 18431907100);the Program of Shanghai Academic Research Leader(No.19XD1424600);the National Science&Technology Major Project“Key New Drug Creation and Manufacturing Program”,China(No.2018ZX09711002-006)for financial support。
We report herein a palladium-catalyzed diarylative dearomatization of indole by employing thioester and arylboronic acid as the aryl electrophiles.The reaction involved a decarbonylation/migratory insertion/terminal S...
the National Natural Science Foundation of China(Nos.U1604285,21772032 and 21702051);Program for Changjiang Scholars and Innovative Research Team in University(PCSIRT)of Ministry of Education of China(No.IRT1061);the 111 Project(No.D17007);Henan Provincial Natural Science Foundation(No.162300410180);Key Project of Henan Educational Committee(No.18A150009);Program for Innovative Research Team of Science and Technology in the University of Henan Province(No.18IRTSTHN004)。
We report a 2-iodoxybenzoic acid(IBX)-mediated intarmolecular oxidative spiro-fused tandem cyclization reaction of tryptophan analogs bearing an N-arylamides side-chain to rapidly afford polycyclic spiroindolines feat...
financial support from the National Natural Science Foundation of China(Nos.21672200,21772185,21801233);the assistance of the product characterization from the Chemistry Experiment Teaching Center of University of Science and Technology of China;supported by China Postdoctoral Science Foundation(No.2018M632532);the Strategic Priority Research Program of the Chinese Academy of Sciences(No.XDB20000000)。
An electrochemical amino-azidation of 2-aminostyre ne with sodium azide(NaN3)was developed,which can be carried out smoothly in water under metal-free condition,affording a series of 3-azido indolines with high yields.
National Natural Science Foundation of China(Nos.21702121,91856119 and 21622201);the Science and Technology Department of Hubei Province(Nos.2016CFA050 and 2017AHB047);the Program of Introducing Talents of Discipline to Universities of China(111 Program,No.B17019)。
Enantiomerically pure 2-substituted indolines are an important class of nitrogen heterocycles that occur frequently in many alkaloid natural products and biologically active compounds.Consequently,the synthesis of suc...