000177223 001__ 177223
000177223 005__ 20190316235355.0
000177223 0247_ $$2doi$$a10.1055/s-0031-1290589
000177223 02470 $$2ISI$$a000303104400003
000177223 037__ $$aARTICLE
000177223 245__ $$aSynthesis of 1-[(Triisopropylsilyl)ethynyl]-1 lambda(3),2-benziodoxol-3(1H)-one and Alkynylation of Indoles, Thiophenes, and Anilines
000177223 269__ $$a2012
000177223 260__ $$c2012
000177223 336__ $$aJournal Articles
000177223 520__ $$aAn efficient procedure was developed for the synthesis of 1-[(triisopropylsilyl)ethynyl]-1 lambda(3),2-benziodoxol-3(1H)-one on a 100-mmol (36-g) scale. The benziodoxolone can be used for the gold-catalyzed direct alkynylation of indole, 2-hexylthiophene, or N,N-dibenzylaniline on a 5- to 10-mmol scale.
000177223 6531_ $$aalkynes
000177223 6531_ $$aarenes
000177223 6531_ $$acatalysis
000177223 6531_ $$aheterocycles
000177223 6531_ $$aiodine
000177223 6531_ $$aHypervalent Iodine
000177223 6531_ $$aHeterocycles
000177223 6531_ $$aGold
000177223 6531_ $$aChemistry
000177223 6531_ $$aReagent
000177223 6531_ $$aEbx
000177223 6531_ $$aElectrophilic Alkynylation
000177223 700__ $$0243585$$g183304$$aBrand, Jonathan P.
000177223 700__ $$aWaser, Jerome$$g181574$$0243584
000177223 773__ $$j44$$tSynthesis-Stuttgart$$q1155-1158
000177223 8564_ $$uhttps://infoscience.epfl.ch/record/177223/files/synthesis2012-1155GreenAccess.pdf$$zn/a$$s629105$$yn/a
000177223 909C0 $$xU11811$$0252236$$pLCSO
000177223 909CO $$ooai:infoscience.tind.io:177223$$qGLOBAL_SET$$pSB$$particle
000177223 917Z8 $$x181574
000177223 917Z8 $$x181574
000177223 937__ $$aEPFL-ARTICLE-177223
000177223 973__ $$rREVIEWED$$sPUBLISHED$$aEPFL
000177223 980__ $$aARTICLE