A mild,green,convenient and scalable N-bromosuccinimide(NBS)promoted direct phosphorylation strategy of secondary phosphine oxides and alcohols for the synthesis of various phosphinate esters was developed.A variety o...
the Natural Science Foundation of Xinjiang Province(No. 2016D01C009);the Educational Commission of Xinjiang(No. XJEDU2017S053)for financial support
A facile transformation of alkynes into α-amino ketones by an N-bromosuccinimide-mediated one-pot cascade strategy is described. A variety of α-amino ketones are obtained in moderate to good yields under mild condit...
We are grateful for the financial support from the National Natural Science Foundation of China (Nos. 21472188, 21690074),the State Key Laboratory of Fine Chemicals (No. KF1503) and the Youth Innovation Promotion Association of Chinese Academy of Sciences (No, 2014167).
An efficient dual stereocontrot in iridium-catalyzed hydrogenation of 1-substituted 3,4-dihydroisoquinolines was realized by tuning the amount of N-bromosuccinimide using chiral ligand of single configuration, providi...
An efficient and facile approach for tetrachlorosilane as an in situ mediated transformation via a one-pot, synthesis of vicinal bromoazides through the generation of BrN3 from azidochlorosilane and N-bromosuccinimide...
Council of Scientific and Industrial Research(CSIR),New Delhi,Government of India for thefinancial support under major research project(No.01(2391)/10/EMR-II)
An easy and rapid method for the α-bromination of ketones using N-bromosuccinimide (NBS) catalyzed by silica gel in methanol under reflux conditions was developed. The expected products were formed in excellent iso...
Supported by the National Natural Science Foundation of China(Nos.20572066, 20906059) and the Natural Science Founda- tion of Shaanxi Province of China(No .2009JM2011).
An efficient method for the one-pot synthesis of 2-oxazolines from ethyl a-cyanocinnamate derivatives with acetamide and N-bromosuccinimide(NBS) in the presence of K3PO4 was developed. The reaction was performed smo...
the Fundamental Research Funds for the Central Universities(No.DUT12LK07).Dr.Bao thanks financial support from the Fundamental Research Funds for the Central Universities(No. DUT11SM01)
A novel and convenient way has been developed for the preparation of bromoallenes from propargyl alcohols by the reagent combination of N-bromosuccinimide and dimethyl sulfide. Bromoallenes with high regioselectivity ...
Supporting intbrmation tbr this article is available on the WWW under http://dx.doi.org/10.1002/cjoc.201200028 or from the author.Acknowledgement This work was supported by the National Natural Science Foundation of China (Nos. 21102105 and 21072153).
A highly practical method to access unsymmetrical and symmetrical thiosulfonates in moderate to excellent yields has been developed through NBS-promoted sulfenylation of sulfinates with disulfides. The present process...
supported by National Natural Science Foundation of China(No30873153);the Key Projects of Shanghai in Biomedical(No08431902700);the Scientific Research Foundation of State Education Ministry for the Returned Overseas Chinese Scholars
An efficient and mild protocol for bromination of aryl azides with N-bromosuccinimide(NBS) under FeCl_3 catalysis in 1,2- dichloroethane was developed.It is proved to be an efficient method for obtaining brominated ...