Regioselective 1,4-Conjugate Addition of Grignard Reagents to Nitrodienes in the Presence of Catalytic Amounts of Zn(II) Salts
Author:
Affiliation:
1. Hunter Laboratory, Department of Chemistry, Clemson University, Clemson, South Carolina 29634-0973, United States
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/ol500114m
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1. Following the Lead from Nature: Divergent Pathways in Natural Product Synthesis and Diversity-Oriented Synthesis
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3. Conjugate Addition Reactions of N-Carbamoyl-4-pyridones and 2,3-Dihydropyridones with Grignard Reagents in the Absence of Cu(I) Salts
4. Regio- and Stereoselectivity in the Reactions of Organometallic Reagents with an Electron-Deficient and an Electron-Rich Vinyloxirane: Applications for Sequential Bis-Allylic Substitution Reactions in the Generation of Vicinal Stereogenic Centers
5. Conjugate Addition Reactions of N-Carbamoyl-4-Pyridones with Organometallic Reagents
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