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Catalytic enantioselective Reformatsky reaction with ketones.
Chem Commun (Camb). 2008 Jun 14CC

Abstract

Chiral tertiary alcohols were obtained with good yields and enantioselectivities via a catalytic Reformatsky reaction with ketones, including the challenging diaryl ketones, using chiral BINOL derivatives.

Authors+Show Affiliations

Department of Organic and Molecular Inorganic Chemistry, Stratingh Institute for Chemistry, University of Groningen, Nijenborgh 4, 9747 AG, Groningen, The Netherlands.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

18506247

Citation

Fernández-Ibáñez, M Angeles, et al. "Catalytic Enantioselective Reformatsky Reaction With Ketones." Chemical Communications (Cambridge, England), 2008, pp. 2571-3.
Fernández-Ibáñez MA, Maciá B, Minnaard AJ, et al. Catalytic enantioselective Reformatsky reaction with ketones. Chem Commun (Camb). 2008.
Fernández-Ibáñez, M. A., Maciá, B., Minnaard, A. J., & Feringa, B. L. (2008). Catalytic enantioselective Reformatsky reaction with ketones. Chemical Communications (Cambridge, England), (22), 2571-3. https://doi.org/10.1039/b801749b
Fernández-Ibáñez MA, et al. Catalytic Enantioselective Reformatsky Reaction With Ketones. Chem Commun (Camb). 2008 Jun 14;(22)2571-3. PubMed PMID: 18506247.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Catalytic enantioselective Reformatsky reaction with ketones. AU - Fernández-Ibáñez,M Angeles, AU - Maciá,Beatriz, AU - Minnaard,Adriaan J, AU - Feringa,Ben L, Y1 - 2008/04/01/ PY - 2008/5/29/pubmed PY - 2008/8/19/medline PY - 2008/5/29/entrez SP - 2571 EP - 3 JF - Chemical communications (Cambridge, England) JO - Chem Commun (Camb) IS - 22 N2 - Chiral tertiary alcohols were obtained with good yields and enantioselectivities via a catalytic Reformatsky reaction with ketones, including the challenging diaryl ketones, using chiral BINOL derivatives. SN - 1359-7345 UR - https://www.unboundmedicine.com/medline/citation/18506247/Catalytic_enantioselective_Reformatsky_reaction_with_ketones_ L2 - https://doi.org/10.1039/b801749b DB - PRIME DP - Unbound Medicine ER -