Zn-proline catalyzed direct aldol reaction in aqueous media.Chem Commun (Camb). 2003 May 07CC
Abstract
Zn complexes of proline, lysine and arginine are efficient catalysts for the aldol addition of p-nitrobenzaldehyde and acetone in aqueous medium, giving quantitative yields and enantiomeric excesses up to 56% with 5 mol% of the catalysts at room temperature.
Pub Type(s)
Journal Article
Language
eng
PubMed ID
12772917
Citation
Darbre, Tamis, and Miguel Machuqueiro. "Zn-proline Catalyzed Direct Aldol Reaction in Aqueous Media." Chemical Communications (Cambridge, England), 2003, pp. 1090-1.
Darbre T, Machuqueiro M. Zn-proline catalyzed direct aldol reaction in aqueous media. Chem Commun (Camb). 2003.
Darbre, T., & Machuqueiro, M. (2003). Zn-proline catalyzed direct aldol reaction in aqueous media. Chemical Communications (Cambridge, England), (9), 1090-1.
Darbre T, Machuqueiro M. Zn-proline Catalyzed Direct Aldol Reaction in Aqueous Media. Chem Commun (Camb). 2003 May 7;(9)1090-1. PubMed PMID: 12772917.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Zn-proline catalyzed direct aldol reaction in aqueous media.
AU - Darbre,Tamis,
AU - Machuqueiro,Miguel,
PY - 2003/5/30/pubmed
PY - 2004/4/15/medline
PY - 2003/5/30/entrez
SP - 1090
EP - 1
JF - Chemical communications (Cambridge, England)
JO - Chem Commun (Camb)
IS - 9
N2 - Zn complexes of proline, lysine and arginine are efficient catalysts for the aldol addition of p-nitrobenzaldehyde and acetone in aqueous medium, giving quantitative yields and enantiomeric excesses up to 56% with 5 mol% of the catalysts at room temperature.
SN - 1359-7345
UR - https://www.unboundmedicine.com/medline/citation/12772917/Zn_proline_catalyzed_direct_aldol_reaction_in_aqueous_media_
DB - PRIME
DP - Unbound Medicine
ER -
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