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https://hdl.handle.net/10356/102819
Title: | Enantioselective addition of diphenylphosphine to 3-methyl-4-nitro-5-alkenylisoxazoles | Authors: | Chew, Renta Jonathan Huang, Yinhua Li, Yongxin Pullarkat, Sumod A. Leung, Pak-Hing |
Keywords: | DRNTU::Science::Chemistry::Organic chemistry | Issue Date: | 2013 | Source: | Chew, R. J., Huang, Y., Li, Y., Pullarkat, S. A., & Leung, P. H. (2013). Enantioselective addition of diphenylphosphine to 3-methyl-4-nitro-5-alkenylisoxazoles. Advanced Synthesis & Catalysis, 355(7), 1403-1408. | Series/Report no.: | Advanced Synthesis & Catalysis | Abstract: | An enantioselective Michael addition reaction of diphenylphosphine to substituted alkenylisoxazoles has been developed. The reaction proceeds efficiently under mild conditions with high yields (up to 99%) and moderate to excellent enantioselectivities (up to 92%) thus providing a hitherto unavailable direct access to a library of chiral tertiary phosphine-functionalized isoxazoles. | URI: | https://hdl.handle.net/10356/102819 http://hdl.handle.net/10220/19200 |
ISSN: | 1615-4150 | DOI: | 10.1002/adsc.201300164 | Schools: | School of Physical and Mathematical Sciences | Rights: | © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | Fulltext Permission: | none | Fulltext Availability: | No Fulltext |
Appears in Collections: | SPMS Journal Articles |
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