Cu-catalyzed selective mono-N-pyridylation: Direct access to 2-aminoDMAP/sulfonamides as bifunctional organocatalysts
dc.citation.epage | 1611 | en_US |
dc.citation.issueNumber | 4 | en_US |
dc.citation.spage | 1604 | en_US |
dc.citation.volumeNumber | 78 | en_US |
dc.contributor.author | Isik, M. | en_US |
dc.contributor.author | Tanyeli, C. | en_US |
dc.date.accessioned | 2016-02-08T09:40:35Z | |
dc.date.available | 2016-02-08T09:40:35Z | |
dc.date.issued | 2013 | en_US |
dc.department | Institute of Materials Science and Nanotechnology (UNAM) | en_US |
dc.description.abstract | Direct and selective mono-N-pyridylation of trans-(R,R)-cyclohexane-1,2- diamine is described here. Facile preparation of a novel chiral 2-aminoDMAP core catalaphore via Cu catalysis has led to the development of various sulfonamide/2-aminoDMAPs as bifunctional acid/base organocatalysts (most in two steps overall), which have been shown to very effectively promote asymmetric conjugate addition of acetylacetone to trans-β-nitroolefins with good to excellent yields (87-93%) and enantioselectivites (up to 99%). © 2013 American Chemical Society. | en_US |
dc.description.provenance | Made available in DSpace on 2016-02-08T09:40:35Z (GMT). No. of bitstreams: 1 bilkent-research-paper.pdf: 70227 bytes, checksum: 26e812c6f5156f83f0e77b261a471b5a (MD5) Previous issue date: 2013 | en |
dc.identifier.doi | 10.1021/jo302713b | en_US |
dc.identifier.issn | 223263 | |
dc.identifier.uri | http://hdl.handle.net/11693/21071 | |
dc.language.iso | English | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1021/jo302713b | en_US |
dc.source.title | Journal of Organic Chemistry | en_US |
dc.subject | Acetylacetone | en_US |
dc.subject | Asymmetric conjugate addition | en_US |
dc.subject | Bi-functional | en_US |
dc.subject | Cu catalysis | en_US |
dc.subject | Enantioselectivites | en_US |
dc.subject | Facile preparation | en_US |
dc.subject | Nitroolefins | en_US |
dc.subject | Organocatalysts | en_US |
dc.subject | Acetone | en_US |
dc.subject | Catalysis | en_US |
dc.subject | Catalysts | en_US |
dc.subject | acetylacetone | en_US |
dc.subject | copper | en_US |
dc.subject | sulfonamide | en_US |
dc.subject | article | en_US |
dc.subject | catalysis | en_US |
dc.subject | catalyst | en_US |
dc.subject | chemical reaction | en_US |
dc.subject | chirality | en_US |
dc.subject | enantioselectivity | en_US |
dc.title | Cu-catalyzed selective mono-N-pyridylation: Direct access to 2-aminoDMAP/sulfonamides as bifunctional organocatalysts | en_US |
dc.type | Article | en_US |
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