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).
Original language | English |
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Pages (from-to) | 814-820 |
Number of pages | 7 |
Journal | Organic and Biomolecular Chemistry |
Volume | 11 |
Issue number | 5 |
DOIs | |
Publication status | Published - 7 Feb 2013 |
Scopus Subject Areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry