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Enantioselective synthesis of tertiary α-hydroxyketones from unfunctionalized ketones: palladium-catalyzed asymmetric allylic alkylation of enolates.
Angew Chem Int Ed Engl. 2012 Aug 13; 51(33):8290-3.AC

Authors+Show Affiliations

Department of Chemistry, Stanford University, Stanford, CA 94305-5080, USA. bmtrost@stanford.eduNo affiliation info availableNo affiliation info available

Pub Type(s)

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

Language

eng

PubMed ID

22829317

Citation

Trost, Barry M., et al. "Enantioselective Synthesis of Tertiary Α-hydroxyketones From Unfunctionalized Ketones: Palladium-catalyzed Asymmetric Allylic Alkylation of Enolates." Angewandte Chemie (International Ed. in English), vol. 51, no. 33, 2012, pp. 8290-3.
Trost BM, Koller R, Schäffner B. Enantioselective synthesis of tertiary α-hydroxyketones from unfunctionalized ketones: palladium-catalyzed asymmetric allylic alkylation of enolates. Angew Chem Int Ed Engl. 2012;51(33):8290-3.
Trost, B. M., Koller, R., & Schäffner, B. (2012). Enantioselective synthesis of tertiary α-hydroxyketones from unfunctionalized ketones: palladium-catalyzed asymmetric allylic alkylation of enolates. Angewandte Chemie (International Ed. in English), 51(33), 8290-3. https://doi.org/10.1002/anie.201203663
Trost BM, Koller R, Schäffner B. Enantioselective Synthesis of Tertiary Α-hydroxyketones From Unfunctionalized Ketones: Palladium-catalyzed Asymmetric Allylic Alkylation of Enolates. Angew Chem Int Ed Engl. 2012 Aug 13;51(33):8290-3. PubMed PMID: 22829317.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Enantioselective synthesis of tertiary α-hydroxyketones from unfunctionalized ketones: palladium-catalyzed asymmetric allylic alkylation of enolates. AU - Trost,Barry M, AU - Koller,Raffael, AU - Schäffner,Benjamin, Y1 - 2012/07/24/ PY - 2012/05/11/received PY - 2012/7/26/entrez PY - 2012/7/26/pubmed PY - 2012/12/22/medline SP - 8290 EP - 3 JF - Angewandte Chemie (International ed. in English) JO - Angew Chem Int Ed Engl VL - 51 IS - 33 SN - 1521-3773 UR - https://www.unboundmedicine.com/medline/citation/22829317/Enantioselective_synthesis_of_tertiary_α_hydroxyketones_from_unfunctionalized_ketones:_palladium_catalyzed_asymmetric_allylic_alkylation_of_enolates_ L2 - https://doi.org/10.1002/anie.201203663 DB - PRIME DP - Unbound Medicine ER -