Oxonitriles: A Grignard Addition−Acylation Route to Enamides
Author:
Affiliation:
1. Department of Chemistry and Biochemistry, Duquesne University, Pittsburgh, Pennsylvania 15282-1530
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol0619765
Reference21 articles.
1. Cyclic Oxonitriles: Synergistic Juxtaposition of Ketone and Nitrile Functionalities
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3. A modified Robinson annulation process to α,α-disubstituted-β,γ-unsaturated cyclohexanone system. Application to the total synthesis of nanaimoal
4. Synthesis of macrocyclic enaminolactams by ring expansion reaction of 2-oxocyclododecane-1-carbonitrile with diarylcarbodiimides
5. Cycloalkylations ofN-(?-Halogenoalkyl)-substituted Macrocyclic Imides
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