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Enantioselective synthesis of alpha-tertiary hydroxyaldehydes by palladium-catalyzed asymmetric allylic alkylation of enolates.
J Am Chem Soc. 2007 Jan 17; 129(2):282-3.JA

Authors+Show Affiliations

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

Pub Type(s)

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

Language

eng

PubMed ID

17212401

Citation

Trost, Barry M., et al. "Enantioselective Synthesis of Alpha-tertiary Hydroxyaldehydes By Palladium-catalyzed Asymmetric Allylic Alkylation of Enolates." Journal of the American Chemical Society, vol. 129, no. 2, 2007, pp. 282-3.
Trost BM, Xu J, Reichle M. Enantioselective synthesis of alpha-tertiary hydroxyaldehydes by palladium-catalyzed asymmetric allylic alkylation of enolates. J Am Chem Soc. 2007;129(2):282-3.
Trost, B. M., Xu, J., & Reichle, M. (2007). Enantioselective synthesis of alpha-tertiary hydroxyaldehydes by palladium-catalyzed asymmetric allylic alkylation of enolates. Journal of the American Chemical Society, 129(2), 282-3.
Trost BM, Xu J, Reichle M. Enantioselective Synthesis of Alpha-tertiary Hydroxyaldehydes By Palladium-catalyzed Asymmetric Allylic Alkylation of Enolates. J Am Chem Soc. 2007 Jan 17;129(2):282-3. PubMed PMID: 17212401.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Enantioselective synthesis of alpha-tertiary hydroxyaldehydes by palladium-catalyzed asymmetric allylic alkylation of enolates. AU - Trost,Barry M, AU - Xu,Jiayi, AU - Reichle,Markus, PY - 2007/1/11/pubmed PY - 2007/5/1/medline PY - 2007/1/11/entrez SP - 282 EP - 3 JF - Journal of the American Chemical Society JO - J Am Chem Soc VL - 129 IS - 2 SN - 0002-7863 UR - https://www.unboundmedicine.com/medline/citation/17212401/Enantioselective_synthesis_of_alpha_tertiary_hydroxyaldehydes_by_palladium_catalyzed_asymmetric_allylic_alkylation_of_enolates_ L2 - https://doi.org/10.1021/ja067342a DB - PRIME DP - Unbound Medicine ER -