supported in part by grants from the National Natural Science Foundation of China(NSFC,No.21971212);the Key Project of Innovation Research 2035 Pilot Plan of Southwest University,China(SWU-XDZD22007);the Research Fund for International Young Scientists from International(Regional)Cooperation and Exchange Program of NSFC(21850410447);the Research Funds for the Central Universities of China(XDJK2020C031).
Alkaloids are one of the prominent members in the development of new antimicrobial agents.This work discovered a class of alkaloid quinazolone-derived imidazolenones as novel structural type of antibacterial agents wi...
The National Natural Science Foundation of China(Nos.21901203,22171225,21925108);the Education Department of Shaanxi Province(No.20JK0934)are acknowledged for financial support.
The first intermolecular electrophilic dearomatization of halonaphthols with benzyl/allyl bromides is described. Halonaphthols are used as carbon-nucleophiles in dearomatization to form three-dimensional cyclic enones...
This work was supported by the National Natural Science Foundation of China(U19A2014,21890723).
A highly enantioselective 1,3-dipolar cycloaddition ofα-substituted diazoesters with exocyclic enones was achieved with chiral scandium(III)/N,N’-dioxide complex as the catalyst.This protocol provided a facile and e...
This project was financially supported by the Science,Technology and Innovation Commission of Shenzhen(Nos.KQTD20150717103157174,JCYJ20170817104350391);the National Natural Science Foundation of China(No.21801118);the Guangdong Provincial Key Laboratory of Catalysis(No.2020B121201002).
Main observation and conclusion The enantioselective hydrogenation of endocyclic enones has been a historical problem for homogeneous catalysis.We herein report an efficient method to reduce endocyclic enones with mol...
the financial support from the National Natural Science Foundation of China(No.21921002);the NationalScience and Technology Major Project of the Ministry of Science and Technology of the People’s Republic of China(No.2018ZX09711001-005-004);the Fundamental Research Funds for the Central Universities(No.2012017yjsy210)。
A convergent approach to 1,5-hydroxy ketones,the general precursors for constructing the C ring of bryostatins,has been developed via a Zn/Cu-promoted conjugate addition of a-hydroxy iodides with enones.The reaction l...
Supported by the National Natural Science Foundation of China(Nos.21772001, 21372008), the Natural Science Foundation of Education Administration of Anhui Province, China(No.KJ2016A267), the Special and Excellent Research Fund of Anhui Normal Universit and the Doctoral Scientific Research Foundation of Anhui Normal University, China(No.2016XJJ110).
A convenient and efficient method was developed for the synthesis of 2,2'-(arylmethylene)bis(3-hydrox- ycyclohex-2-enone) derivatives via the oleylamine-catalyzed tandem Knoevenagel/Michael addition reactions of ...
Supports from the National Natural Science Foundation of China (Nos. 21272257, 21274041 and 21474028)
NTrifluoromethyl and cyclopropyl substituted 2-isoxazolines were synthesized via a DBU-promoted domino reaction of β-trifluoromethyl-/β-cyclopropyl-substituted enones with hydroxylamine. The domino reaction consists...
The study has shown free radical processes during modeling of Parkinson Disease (PD) with rotenone. We isolated striatum, brainstem, neocortex, cerebellum, spinal cord, thymus, heart, and liver of rats after rotenone ...
Supported by the National Natural Science Foundation of China (Nos.20773147, 21073211, 21174133).
Five novel tropos (3R,4R)- and/or (3S,4S)-N-benzyltartarimide-derived biphenylphosphite ligands were synthesized and applied in the Cu-catalyzed asymmetric conjugate addition of diethylzinc to cyclic enones with u...
A series of new hydantoin compounds was synthesized with 3-bromo phenylacetic acid and 3,4-dimethylbromobenzene as starting material, 7-bromo-2-tetralone and 2-bromo-5,6,8,9-tetrahydro-7-benzocycloheptenone as interme...