Solvent-Free, Microwave-Assisted, One-Pot Synthesis of 2-Acetyl-N,3-diaryl-4-nitro-butanamides
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397911003707113
Reference16 articles.
1. Asymmetric Michael Additions to Nitroalkenes
2. Efficient Proline-Catalyzed Michael Additions of Unmodified Ketones to Nitro Olefins
3. Highly Enantioselective Direct Conjugate Addition of Ketones to Nitroalkenes Promoted by A Chiral Primary Amine−Thiourea Catalyst
4. A Chiral Primary Amine Thiourea Catalyst for the Highly Enantioselective Direct Conjugate Addition of α,α-Disubstituted Aldehydes to Nitroalkenes
5. Perekalin , V. V. ; Lipina , E. S. ; Berestovitskaya , V. M. ; Efremov , D. A.Nitroalkenes: Conjugated Nitro Compounds; John Wiley : Chichester , 1994 ; ch. 2 , p. 53 .
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1. One-pot three-component reaction for efficient and facile synthesis of γ-nitrocarbonyl compounds under solvent-free conditions;Chemical Research in Chinese Universities;2015-03-20
2. An efficient green protocol for the preparation of acetoacetamides and application of the methodology to a one-pot synthesis of Biginelli dihydropyrimidines. Expansion of dihydropyrimidine topological chemical space;RSC Advances;2015
3. 2,2,6-Trimethyl-4H-1,3-dioxin-4-one;Synlett;2012-05-29
4. ChemInform Abstract: Solvent-Free, Microwave-Assisted, One-Pot Synthesis of 2-Acetyl-N,3-diaryl-4-nitrobutanamides.;ChemInform;2011-07-14
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