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Design of chiral bifunctional secondary amine catalysts for asymmetric enamine catalysis.
Chem Commun (Camb). 2008 Nov 21CC

Abstract

A series of binaphthyl-based secondary amine catalysts containing various functional groups have been designed as new chiral bifunctional amine catalysts. These chiral organocatalysts have been successfully applied to several asymmetric reactions via enamine intermediates and exhibit unique reactivity and selectivity in comparison with proline and its derivatives.

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Publisher Full Text (DOI)

Authors+Show Affiliations

Kano T
Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan.
Maruoka K
No affiliation info available

MeSH

AlcoholsAldehydesAminesCatalysisKetonesMolecular StructureStereoisomerism

Pub Type(s)

Journal Article

Language

eng

PubMed ID

18997926

Citation

Kano, Taichi, and Keiji Maruoka. "Design of Chiral Bifunctional Secondary Amine Catalysts for Asymmetric Enamine Catalysis." Chemical Communications (Cambridge, England), 2008, pp. 5465-73.
Kano T, Maruoka K. Design of chiral bifunctional secondary amine catalysts for asymmetric enamine catalysis. Chem Commun (Camb). 2008.
Kano, T., & Maruoka, K. (2008). Design of chiral bifunctional secondary amine catalysts for asymmetric enamine catalysis. Chemical Communications (Cambridge, England), (43), 5465-73. https://doi.org/10.1039/b809301f
Kano T, Maruoka K. Design of Chiral Bifunctional Secondary Amine Catalysts for Asymmetric Enamine Catalysis. Chem Commun (Camb). 2008 Nov 21;(43)5465-73. PubMed PMID: 18997926.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Design of chiral bifunctional secondary amine catalysts for asymmetric enamine catalysis. AU - Kano,Taichi, AU - Maruoka,Keiji, Y1 - 2008/09/10/ PY - 2008/11/11/pubmed PY - 2009/1/24/medline PY - 2008/11/11/entrez SP - 5465 EP - 73 JF - Chemical communications (Cambridge, England) JO - Chem Commun (Camb) IS - 43 N2 - A series of binaphthyl-based secondary amine catalysts containing various functional groups have been designed as new chiral bifunctional amine catalysts. These chiral organocatalysts have been successfully applied to several asymmetric reactions via enamine intermediates and exhibit unique reactivity and selectivity in comparison with proline and its derivatives. SN - 1359-7345 UR - https://www.unboundmedicine.com/medline/citation/18997926/Design_of_chiral_bifunctional_secondary_amine_catalysts_for_asymmetric_enamine_catalysis_ L2 - https://doi.org/10.1039/b809301f DB - PRIME DP - Unbound Medicine ER -