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Highly enantioselective proline-catalysed direct aldol reaction of chloroacetone and aromatic aldehydes.
Chemistry. 2012 Apr 23; 18(17):5188-90.C

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Publisher Full Text (DOI)

Authors+Show Affiliations

Martínez-Castañeda Á
Departamento de Química Orgánica e Inorgánica, Universidad de Oviedo, C/Julián Clavería 8, 33006, Oviedo, Spain.
Poladura B
No affiliation info available
Rodríguez-Solla H
No affiliation info available
Concellón C
No affiliation info available
del Amo V
No affiliation info available

MeSH

AcetoneAldehydesCatalysisGuanidineMolecular StructureProlineStereoisomerism

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

22434507

Citation

Martínez-Castañeda, Ángel, et al. "Highly Enantioselective Proline-catalysed Direct Aldol Reaction of Chloroacetone and Aromatic Aldehydes." Chemistry (Weinheim an Der Bergstrasse, Germany), vol. 18, no. 17, 2012, pp. 5188-90.
Martínez-Castañeda Á, Poladura B, Rodríguez-Solla H, et al. Highly enantioselective proline-catalysed direct aldol reaction of chloroacetone and aromatic aldehydes. Chemistry. 2012;18(17):5188-90.
Martínez-Castañeda, Á., Poladura, B., Rodríguez-Solla, H., Concellón, C., & del Amo, V. (2012). Highly enantioselective proline-catalysed direct aldol reaction of chloroacetone and aromatic aldehydes. Chemistry (Weinheim an Der Bergstrasse, Germany), 18(17), 5188-90. https://doi.org/10.1002/chem.201103667
Martínez-Castañeda Á, et al. Highly Enantioselective Proline-catalysed Direct Aldol Reaction of Chloroacetone and Aromatic Aldehydes. Chemistry. 2012 Apr 23;18(17):5188-90. PubMed PMID: 22434507.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Highly enantioselective proline-catalysed direct aldol reaction of chloroacetone and aromatic aldehydes. AU - Martínez-Castañeda,Ángel, AU - Poladura,Belén, AU - Rodríguez-Solla,Humberto, AU - Concellón,Carmen, AU - del Amo,Vicente, Y1 - 2012/03/20/ PY - 2011/11/21/received PY - 2012/02/24/revised PY - 2012/3/22/entrez PY - 2012/3/22/pubmed PY - 2012/7/4/medline SP - 5188 EP - 90 JF - Chemistry (Weinheim an der Bergstrasse, Germany) JO - Chemistry VL - 18 IS - 17 SN - 1521-3765 UR - https://www.unboundmedicine.com/medline/citation/22434507/Highly_enantioselective_proline_catalysed_direct_aldol_reaction_of_chloroacetone_and_aromatic_aldehydes_ L2 - https://doi.org/10.1002/chem.201103667 DB - PRIME DP - Unbound Medicine ER -