Asymmetric catalysis with chiral primary amine-based organocatalysts.Chem Commun (Camb). 2009 Apr 14CC
Abstract
In the past few years, primary amine catalysts derived from natural amino acids, Cinchona alkaloids and other chiral amines have emerged as readily available, highly versatile and extremely powerful catalysts in asymmetric synthesis. They have been demonstrated to be effective catalysts in a wide range of enantioselective organic reactions. In comparison with secondary amine-mediated transformations, the use of primary amine organocatalysts has often been shown to be complementary or superior.
Links
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Review
Language
eng
PubMed ID
19319412
Citation
Xu, Li-Wen, et al. "Asymmetric Catalysis With Chiral Primary Amine-based Organocatalysts." Chemical Communications (Cambridge, England), 2009, pp. 1807-21.
Xu LW, Luo J, Lu Y. Asymmetric catalysis with chiral primary amine-based organocatalysts. Chem Commun (Camb). 2009.
Xu, L. W., Luo, J., & Lu, Y. (2009). Asymmetric catalysis with chiral primary amine-based organocatalysts. Chemical Communications (Cambridge, England), (14), 1807-21. https://doi.org/10.1039/b821070e
Xu LW, Luo J, Lu Y. Asymmetric Catalysis With Chiral Primary Amine-based Organocatalysts. Chem Commun (Camb). 2009 Apr 14;(14)1807-21. PubMed PMID: 19319412.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Asymmetric catalysis with chiral primary amine-based organocatalysts.
AU - Xu,Li-Wen,
AU - Luo,Jie,
AU - Lu,Yixin,
Y1 - 2009/03/06/
PY - 2009/3/26/entrez
PY - 2009/3/26/pubmed
PY - 2009/6/9/medline
SP - 1807
EP - 21
JF - Chemical communications (Cambridge, England)
JO - Chem Commun (Camb)
IS - 14
N2 - In the past few years, primary amine catalysts derived from natural amino acids, Cinchona alkaloids and other chiral amines have emerged as readily available, highly versatile and extremely powerful catalysts in asymmetric synthesis. They have been demonstrated to be effective catalysts in a wide range of enantioselective organic reactions. In comparison with secondary amine-mediated transformations, the use of primary amine organocatalysts has often been shown to be complementary or superior.
SN - 1359-7345
UR - https://www.unboundmedicine.com/medline/citation/19319412/Asymmetric_catalysis_with_chiral_primary_amine_based_organocatalysts_
L2 - https://doi.org/10.1039/b821070e
DB - PRIME
DP - Unbound Medicine
ER -