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Fast and efficient one step synthesis of dienamides.
Org Biomol Chem. 2009 May 21; 7(10):2170-5.OB

Abstract

A fast and efficient one-step approach to the synthesis of dienamides is reported. This concise methodology relies on the use of imides as reactive intermediates and allows for the preferential formation of Z,E-dienamides in good yields.

Links

Publisher Full Text (DOI)

Authors+Show Affiliations

Mathieson JE
WestCHEM, Department of Chemistry, University of Glasgow, Glasgow, UK G12 8QQ.
Crawford JJ
No affiliation info available
Schmidtmann M
No affiliation info available
Marquez R
No affiliation info available

MeSH

AmidesCatalysisCrystallizationCrystallography, X-RayCyclizationImidesMesylatesModels, MolecularMolecular StructureStereoisomerism

Pub Type(s)

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

Language

eng

PubMed ID

19421456

Citation

Mathieson, Jennifer E., et al. "Fast and Efficient One Step Synthesis of Dienamides." Organic & Biomolecular Chemistry, vol. 7, no. 10, 2009, pp. 2170-5.
Mathieson JE, Crawford JJ, Schmidtmann M, et al. Fast and efficient one step synthesis of dienamides. Org Biomol Chem. 2009;7(10):2170-5.
Mathieson, J. E., Crawford, J. J., Schmidtmann, M., & Marquez, R. (2009). Fast and efficient one step synthesis of dienamides. Organic & Biomolecular Chemistry, 7(10), 2170-5. https://doi.org/10.1039/b901797f
Mathieson JE, et al. Fast and Efficient One Step Synthesis of Dienamides. Org Biomol Chem. 2009 May 21;7(10):2170-5. PubMed PMID: 19421456.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Fast and efficient one step synthesis of dienamides. AU - Mathieson,Jennifer E, AU - Crawford,James J, AU - Schmidtmann,Marc, AU - Marquez,Rodolfo, Y1 - 2009/04/16/ PY - 2009/5/8/entrez PY - 2009/5/8/pubmed PY - 2009/10/6/medline SP - 2170 EP - 5 JF - Organic & biomolecular chemistry JO - Org Biomol Chem VL - 7 IS - 10 N2 - A fast and efficient one-step approach to the synthesis of dienamides is reported. This concise methodology relies on the use of imides as reactive intermediates and allows for the preferential formation of Z,E-dienamides in good yields. SN - 1477-0539 UR - https://www.unboundmedicine.com/medline/citation/19421456/Fast_and_efficient_one_step_synthesis_of_dienamides_ L2 - https://doi.org/10.1039/b901797f DB - PRIME DP - Unbound Medicine ER -