Synthesis of β-ketoesters from renewable resources and Meldrum's acid-Reference-Cited by-同舟云学术

Synthesis of β-ketoesters from renewable resources and Meldrum's acid

Published:2014 Issue:91 Volume:4 Page:49556-49559
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Brinkerhoff Rafael C.¹²³,Tarazona Hernan F.¹²³,de Oliveira Patrick M.¹²³,Flores Darlene C.¹²³,Montes D'Oca Caroline Da R.⁴⁵⁶,Russowsky Dennis⁴⁵⁶,Montes D'Oca Marcelo G.¹²³

Affiliation:

1. Universidade Federal do Rio Grande

2. Laboratório Kolbe de Síntese Orgânica

3. Rio Grande-RS, Brazil

4. Universidade Federal do Rio Grande do Sul-UFRGS

5. Laboratório de Síntese Orgânica

6. Porto Alegre-RS, Brazil

Abstract

β-Ketoesters are valuable building blocks for the synthesis of compounds with different biological activities.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA08986C

Reference23 articles.

1. Unified Strategy for Iodine(III)-Mediated Halogenation and Azidation of 1,3-Dicarbonyl Compounds

2. NBS-mediated sequential one-pot synthesis of multifunctionalized thiazoles and thiophenes from 1,3-dicarbonyl compounds and mercaptonitrile salts

3. An efficient synthesis of β-ketoesters via transesterification and its application in Biginelli reaction under solvent-free, catalyst-free conditions

4. Sc(OTf)3-Catalyzed Three-Component Cyclization of Arylamines, β,γ-Unsaturated α-Ketoesters, and 1,3-Dicarbonyl Compounds for the Synthesis of Highly Substituted 1,4-Dihydropyridines and Tetrahydropyridines

5. Synthesis and differential antiproliferative activity of Biginelli compounds against cancer cell lines: Monastrol, oxo-monastrol and oxygenated analogues

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