4.4 Article

A promising enantioselective Diels-Alder dienophile by computer-assisted rational design: 2,5-diphenyl-1-vinyl-borolane

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JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN
卷 18, 期 3, 页码 209-214

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SPRINGER
DOI: 10.1023/B:JCAM.0000035200.30340.41

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asymmetric synthesis; boranes; cycloadditions; density functional calculations; ligand design

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Several chiral vinylboranes have been theoretically evaluated as enantioselective Diels - Alder dienophiles. Theoretical results suggest that optically pure 2,5-diphenyl-1-vinyl-borolane should be the reagent of choice for performing such transformations efficiently.

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