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Palladium-catalyzed regio- and enantioselective allylic alkylation of bis allylic carbonates derived from Morita-Baylis-Hillman adducts.
Org Lett. 2007 Sep 27; 9(20):3961-4.OL

Abstract

Morita-Baylis-Hillman diene adducts are used as substrates in the palladium-catalyzed asymmetric allylic alkylation reaction with oxygen and carbon nucleophiles in good regio- and enantioselectivity.

Authors+Show Affiliations

Trost BM
Department of Chemistry, Stanford University, Stanford, California 94305, USA. bmtrost@stanford.edu
Brennan MK
No affiliation info available

MeSH

AlkylationCarbonatesCatalysisModels, MolecularMolecular StructureOxygenPalladiumStereoisomerism

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

17803313

Citation

Trost, Barry M., and Megan K. Brennan. "Palladium-catalyzed Regio- and Enantioselective Allylic Alkylation of Bis Allylic Carbonates Derived From Morita-Baylis-Hillman Adducts." Organic Letters, vol. 9, no. 20, 2007, pp. 3961-4.
Trost BM, Brennan MK. Palladium-catalyzed regio- and enantioselective allylic alkylation of bis allylic carbonates derived from Morita-Baylis-Hillman adducts. Org Lett. 2007;9(20):3961-4.
Trost, B. M., & Brennan, M. K. (2007). Palladium-catalyzed regio- and enantioselective allylic alkylation of bis allylic carbonates derived from Morita-Baylis-Hillman adducts. Organic Letters, 9(20), 3961-4.
Trost BM, Brennan MK. Palladium-catalyzed Regio- and Enantioselective Allylic Alkylation of Bis Allylic Carbonates Derived From Morita-Baylis-Hillman Adducts. Org Lett. 2007 Sep 27;9(20):3961-4. PubMed PMID: 17803313.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Palladium-catalyzed regio- and enantioselective allylic alkylation of bis allylic carbonates derived from Morita-Baylis-Hillman adducts. AU - Trost,Barry M, AU - Brennan,Megan K, Y1 - 2007/09/06/ PY - 2007/9/7/pubmed PY - 2007/11/1/medline PY - 2007/9/7/entrez SP - 3961 EP - 4 JF - Organic letters JO - Org Lett VL - 9 IS - 20 N2 - Morita-Baylis-Hillman diene adducts are used as substrates in the palladium-catalyzed asymmetric allylic alkylation reaction with oxygen and carbon nucleophiles in good regio- and enantioselectivity. SN - 1523-7060 UR - https://www.unboundmedicine.com/medline/citation/17803313/Palladium_catalyzed_regio__and_enantioselective_allylic_alkylation_of_bis_allylic_carbonates_derived_from_Morita_Baylis_Hillman_adducts_ DB - PRIME DP - Unbound Medicine ER -