期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 17, 期 16, 页码 4077-4086出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9ob00545e
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- DST, New Delhi
- UGC, New Delhi
A conformationally rigid chiral bicyclic skeleton tethered bipyridine-Zn(OTf)(2) complex facilitated the enantioselective Friedel-Crafts alkylation of indoles with trans-beta-nitroarylalkenes in an enantioselective manner at elevated temperature. Indoles reacted smoothly with beta-nitroarylalkenes to generate the corresponding 3-(2-nitroalkyl) indoles in good to excellent yields (up to 94%) with moderate to excellent enantioselectivities (up to 91%). The stereochemical outcome of the product from indole and trans-beta-nitrostyrene in the presence of the CRCB tethered bipyridine-Zn(OTf)(2) complex and the DFT calculation of the CRCB tethered bipyridine-Zn: trans-beta-nitrostyrene complex support the si-face attack of indole on trans-beta-nitrostyrene.
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