Abstract
(3R,4R)-2,2,5,5-tetraphenyltetrahydrofuran-3,4-diol was employed as additive in the L-proline-catalyzed Michael addition of acetone to nitroalkenes, resulting in upgrading 8-28% ee in enantiomeric purity of the products compared with those without additives.
Keywords: β-nitrostyrene, chiral catalysts, DMSO, ketones, L-proline, michael addition, nitroalkene, acetone, BINOL, enantioselectivity
Letters in Organic Chemistry
Title:(3R,4R)-2,2,5,5-Tetraphenyltetrahydrofuran-3,4-diol Assisted, L-proline- Catalyzed Michael Addition of Acetone to Nitroalkenes
Volume: 9 Issue: 7
Author(s): Xiaoyun Hu, Zixing Shan and Chang Qing
Affiliation:
Keywords: β-nitrostyrene, chiral catalysts, DMSO, ketones, L-proline, michael addition, nitroalkene, acetone, BINOL, enantioselectivity
Abstract: (3R,4R)-2,2,5,5-tetraphenyltetrahydrofuran-3,4-diol was employed as additive in the L-proline-catalyzed Michael addition of acetone to nitroalkenes, resulting in upgrading 8-28% ee in enantiomeric purity of the products compared with those without additives.
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Cite this article as:
Hu Xiaoyun, Shan Zixing and Qing Chang, (3R,4R)-2,2,5,5-Tetraphenyltetrahydrofuran-3,4-diol Assisted, L-proline- Catalyzed Michael Addition of Acetone to Nitroalkenes, Letters in Organic Chemistry 2012; 9 (7) . https://dx.doi.org/10.2174/157017812802139708
DOI https://dx.doi.org/10.2174/157017812802139708 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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