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Featured researches published by Xinsheng Lei.


RSC Advances | 2018

Cs2CO3-promoted defluorination and functionalization of α-CF3 carbonyl compounds in the presence of N-, O-, and/or S-nucleophiles

Yue Wu; Bingbing Zhang; Yinying Zheng; Yuheng Wang; Xinsheng Lei

A simple, efficient, and mild method for defluorination and functionalization of 3,3,3-trifluoro carbonyl compounds has been developed. In the present method, Cs2CO3 can easily convert α-trifluoromethyl esters, amides, and ketones into β,β-S-, O- and/or N-substituted α,β-unsaturated carbonyl compounds in the presence of N-, O-, and S-nucleophiles with moderate to excellent yields, and furthermore, this transformation with α-trifluoromethyl ester and a series of 2-aminophenols can result in benzooxazoles in good yields.


Heterocyclic Communications | 2017

An improved and scalable synthesis of zolpidem via a CuI/BINOL-mediated tandem reaction of imine and alkyne

Bingbing Zhang; Guangsheng Shan; Qiaoning Ma; Qianqian Xu; Xinsheng Lei

Abstract An improved and scalable method for the synthesis of zolpidem (1), a hypnotic drug, was developed. A two-step sequence involving imine formation and subsequent tandem reaction between an imine and propiolamide in the presence of CuI/BINOL, an efficient promoter for the tandem reaction, is described. Zolpidem was efficiently prepared in a 54% isolated yield and the hemitartrate salt of zolpidem was produced in 37% yield by simple crystallization, without tedious column chromatography. The procedure can be scaled up to >10 g. The yield of 1 increased to 83% following isolation of the intermediate imine 5.


Molecules | 2014

Synthesis of ∆3-2-Hydroxybakuchiol Analogues and Their Growth Inhibitory Activity against Rat UMR106 Cells

Qun Zhao; Qianqian Xu; Guangsheng Shan; Chao Dong; Hong Zhang; Xinsheng Lei

A series of ∆3-2-hydroxybakuchiol analogues have been synthesized and tested for their growth inhibitory activity against rat UMR106 cells by using the MTT method. Some of them exhibit enhanced activities compared with the natural product, and the preliminary SAR profile shows that the chain tail on the natural product could be subtly modified to enhance the activity and the aromatic moiety or the terminal olefin on the main chain can also be modified without any evident loss of activity. The stereo-configuration of the quaternary chiral center has an important influence on the activity.


Tetrahedron Letters | 2010

Synthesis of imidazo[1,2a]pyridines via three-component reaction of 2-aminopyridines, aldehydes and alkynes

Ping Liu; Li-song Fang; Xinsheng Lei; Guo-Qiang Lin


European Journal of Organic Chemistry | 2011

Tandem Amination/Cycloisomerization of Aryl Propargylic Alcohols with 2-Aminopyridines as an Expedient Route to Imidazo[1,2-a]pyridines

Ping Liu; Chun-Lin Deng; Xinsheng Lei; Guo-Qiang Lin


Tetrahedron | 2013

A facile asymmetric synthesis of Δ3-2-Hydroxybakuchiol, Bakuchiol and ent-Bakuchiol

Qianqian Xu; Qun Zhao; Guangsheng Shan; Xi-Cheng Yang; Qi-Yuan Shi; Xinsheng Lei


Tetrahedron | 2011

A facile synthesis of 1,4-dideoxy-1,4-imino-l-ribitol (LRB) and (−)-8a-epi-swainsonine from d-glutamic acid

Xiao-Ling Wang; Wen-Feng Huang; Xinsheng Lei; Bang-Guo Wei; Guo-Qiang Lin


Tetrahedron Letters | 2010

Asymmetric synthesis of ceramide sphingolipid based on (2S,3S,4S)-3,4-dihydroxy-5-(hydroxymethyl)pyrrolidine lactam

Wen-Feng Huang; Qian-Ru Li; Lu-Men Chao; Xinsheng Lei; Bang-Guo Wei


Synlett | 2012

A Complementary Approach to 3,5-Substituted Pyrazoles with Tosylhydrazones and Terminal Alkynes Mediated by TfOH

Ping Liu; Qian-Qian Xu; Chao Dong; Xinsheng Lei; Guo-Qiang Lin


Tetrahedron | 2016

Facile synthesis of fluorovinyl-containing lactams via ring-closing metathesis of N-substituted 2-fluoroallylamides

Yang Li; Kai Li; Yue Wu; Qiaoning Ma; Xinsheng Lei

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