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Iridium-catalyzed asymmetric hydroalkynylation reactions of oxabenzonorbornadienes†
Jun Hu,Qingjing Yang,Jianbin Xu,Chao Huang,Baomin Fan,Jun Wang,Chengyuan Lin,Albert S. C. Chan
Organic & Biomolecular Chemistry Pub Date : 11/13/2012 00:00:00 , DOI:10.1039/C2OB26775F
Abstract

Oxabenzonorbornadienes were found to be suitable substrates for asymmetric hydroalkynylation reactions. Catalyzed by the complex of [Ir(COD)Cl]2 and (R)-SYNPHOS, oxabenzonorbornadienes and terminal alkynes could react smoothly to give the alkynylated products in moderate to good yields (up to 93% yield) and enantioselectivities (up to 85% ee).

Graphical abstract: Iridium-catalyzed asymmetric hydroalkynylation reactions of oxabenzonorbornadienes
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