000212317 001__ 212317
000212317 005__ 20181203024018.0
000212317 0247_ $$2doi$$a10.1039/c5sc01909e
000212317 022__ $$a2041-6520
000212317 02470 $$2ISI$$a000359214100009
000212317 037__ $$aARTICLE
000212317 245__ $$aEnantioselective palladium(0)-catalyzed intramolecular cyclopropane functionalization: access to dihydroquinolones, dihydroisoquinolones and the BMS-791325 ring system
000212317 260__ $$aCambridge$$bRoyal Soc Chemistry$$c2015
000212317 269__ $$a2015
000212317 300__ $$a8
000212317 336__ $$aJournal Articles
000212317 520__ $$aTaddol-based phosphoramidite ligands enable enantioselective palladium(0)-catalyzed C-H arylation of cyclopropanes. The cyclized products are obtained in high yields and enantioselectivities. The reported method provides efficient access to a broad range of synthetically attractive cyclopropyl containing dihydroquinolones and dihydroisoquinolones as well as allows for an efficient enantioselective construction of the 7-membered ring of the cyclopropyl indolobenzazepine core of BMS-791325.
000212317 700__ $$0247425$$aPedroni, J.$$g235592
000212317 700__ $$0246952$$aSaget, T.$$g192007
000212317 700__ $$0245585$$aDonets, P. A.$$g213431
000212317 700__ $$0244709$$aCramer, N.$$g206338
000212317 773__ $$j6$$k9$$q5164-5171$$tChemical Science
000212317 909C0 $$0252404$$pLCSA$$xU12340
000212317 909CO $$ooai:infoscience.tind.io:212317$$pSB$$particle
000212317 917Z8 $$x206338
000212317 937__ $$aEPFL-ARTICLE-212317
000212317 973__ $$aEPFL$$rREVIEWED$$sPUBLISHED
000212317 980__ $$aARTICLE