Design of chiral organocatalysts for practical asymmetric synthesis of amino acid derivatives.
Chem Commun (Camb). 2007 Apr 21CC

Abstract

A series of structurally rigid, chiral quaternary ammonium salts and several chiral sec-amine catalysts derived from commercially available (R)- or (S)-binaphthol have been designed as new C(2)-symmetric chiral phase-transfer catalysts and chiral bifunctional amino-catalysts. These chiral organocatalysts have been successfully applied to the highly practical asymmetric synthesis of various amino acid derivatives.

Authors+Show Affiliations

Maruoka K

Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan. maruoka@kuchem.kyoto-u.ac.jp

Ooi T

No affiliation info available

Kano T

No affiliation info available

MeSH

Amino AcidsCatalysisMolecular StructureQuaternary Ammonium CompoundsStereoisomerism

Pub Type(s)

Journal Article

Language

eng

PubMed ID

17406684

Citation

Maruoka, Keiji, et al. "Design of Chiral Organocatalysts for Practical Asymmetric Synthesis of Amino Acid Derivatives." Chemical Communications (Cambridge, England), 2007, pp. 1487-95.

Maruoka K, Ooi T, Kano T. Design of chiral organocatalysts for practical asymmetric synthesis of amino acid derivatives. Chem Commun (Camb). 2007.

Maruoka, K., Ooi, T., & Kano, T. (2007). Design of chiral organocatalysts for practical asymmetric synthesis of amino acid derivatives. Chemical Communications (Cambridge, England), (15), 1487-95.

Maruoka K, Ooi T, Kano T. Design of Chiral Organocatalysts for Practical Asymmetric Synthesis of Amino Acid Derivatives. Chem Commun (Camb). 2007 Apr 21;(15)1487-95. PubMed PMID: 17406684.

* Article titles in AMA citation format should be in sentence-case

TY - JOUR T1 - Design of chiral organocatalysts for practical asymmetric synthesis of amino acid derivatives. AU - Maruoka,Keiji, AU - Ooi,Takashi, AU - Kano,Taichi, Y1 - 2006/12/08/ PY - 2007/4/5/pubmed PY - 2007/7/3/medline PY - 2007/4/5/entrez SP - 1487 EP - 95 JF - Chemical communications (Cambridge, England) JO - Chem Commun (Camb) IS - 15 N2 - A series of structurally rigid, chiral quaternary ammonium salts and several chiral sec-amine catalysts derived from commercially available (R)- or (S)-binaphthol have been designed as new C(2)-symmetric chiral phase-transfer catalysts and chiral bifunctional amino-catalysts. These chiral organocatalysts have been successfully applied to the highly practical asymmetric synthesis of various amino acid derivatives. SN - 1359-7345 UR - https://www.unboundmedicine.com/medline/citation/17406684/Design_of_chiral_organocatalysts_for_practical_asymmetric_synthesis_of_amino_acid_derivatives_ L2 - https://doi.org/10.1039/b613049f DB - PRIME DP - Unbound Medicine ER -

Tags

Design of chiral organocatalysts for practical asymmetric synthesis of amino acid derivatives.Chem Commun (Camb). 2007 Apr 21CC