Abstract
Chiral oxazoline cyanocuprates were prepared and added to conjugated nitroalkenes. Stereoselectivity up to 80% was achieved with the cuprate prepared from the chiral oxazoline derived from (S)- Phenylalaninol.
Keywords: Chiral 2-oxazolines, cuprates, nitroalkenes, stereoselective addition
Letters in Organic Chemistry
Title: Stereoselective Addition of Chiral Oxazoline Cyanocuprates to Conjugated Nitroalkenes
Volume: 4 Issue: 3
Author(s): Francisco A. Marques, Davi C. Silva, Edison P. Wendler, Celso L. Wosch, Quezia B. Cass and Fabiana Batigalhia
Affiliation:
Keywords: Chiral 2-oxazolines, cuprates, nitroalkenes, stereoselective addition
Abstract: Chiral oxazoline cyanocuprates were prepared and added to conjugated nitroalkenes. Stereoselectivity up to 80% was achieved with the cuprate prepared from the chiral oxazoline derived from (S)- Phenylalaninol.
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Cite this article as:
Marques A. Francisco, Silva C. Davi, Wendler P. Edison, Wosch L. Celso, Cass B. Quezia and Batigalhia Fabiana, Stereoselective Addition of Chiral Oxazoline Cyanocuprates to Conjugated Nitroalkenes, Letters in Organic Chemistry 2007; 4 (3) . https://dx.doi.org/10.2174/157017807780737345
DOI https://dx.doi.org/10.2174/157017807780737345 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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