000175638 001__ 175638
000175638 005__ 20181203022645.0
000175638 0247_ $$2doi$$a10.1021/ol300348w
000175638 022__ $$a1523-7060
000175638 02470 $$2ISI$$a000302387800023
000175638 037__ $$aARTICLE
000175638 245__ $$aCopper-Catalyzed Alkylation of Benzoxazoles with Secondary Alkyl Halides
000175638 260__ $$bAmerican Chemical Society$$c2012
000175638 269__ $$a2012
000175638 336__ $$aJournal Articles
000175638 520__ $$aCopper-catalyzed direct alkylation of benzoxazoles using nonactivated secondary alkyl halides has been developed. The best catalyst is a new copper(I) complex (1), and the reactions are promoted by bis[2-(N,N-dimethylamino)ethyl] ether.
000175638 6531_ $$aCarbon-Hydrogen Bonds
000175638 6531_ $$aNickel Pincer Complex
000175638 6531_ $$aC-H Bonds
000175638 6531_ $$aDirect Alkynylation
000175638 6531_ $$aGrignard-Reagents
000175638 6531_ $$aDirect Functionalization
000175638 6531_ $$aDirect Arylation
000175638 6531_ $$aCross-Couplings
000175638 6531_ $$aPalladium
000175638 6531_ $$aBromides
000175638 700__ $$0242980$$g187092$$aRen, Peng
000175638 700__ $$aSalihu, Isuf
000175638 700__ $$0240189$$g148592$$aScopelliti, Rosario
000175638 700__ $$0242979$$g181278$$aHu, Xile
000175638 773__ $$j14$$tOrganic Letters$$k7$$q1748-1751
000175638 909C0 $$xU11810$$0252113$$pLSCI
000175638 909CO $$pSB$$particle$$ooai:infoscience.tind.io:175638
000175638 917Z8 $$x181278
000175638 917Z8 $$x181278
000175638 937__ $$aEPFL-ARTICLE-175638
000175638 973__ $$rREVIEWED$$sPUBLISHED$$aEPFL
000175638 980__ $$aARTICLE