2008
DOI: 10.1055/s-2007-990942
|View full text |Cite
|
Sign up to set email alerts
|

Multicomponent Reactions of Carbonyl Compounds and Derivatives of Cyanoacetic Acid: Synthesis of Carbo- and Heterocycles

Abstract: M u l t i c o m p o n e n t R e a c t i o n s o f C a r b o n y l C o m p o u n d s

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3

Citation Types

0
31
0

Year Published

2008
2008
2017
2017

Publication Types

Select...
10

Relationship

0
10

Authors

Journals

citations
Cited by 81 publications
(31 citation statements)
references
References 85 publications
0
31
0
Order By: Relevance
“…It should be noted that malononitrile is a very convenient reagent for many MCRs due to having a reactive methylene and two cyano groups to build several carbon-carbon and carbon-heteroatom bonds simoltaneously. 29 Thus, a pseudo four-component process takes place and a new series of dicyanoanilines 4 is obtained (Scheme 1). Although there is a few reports on the synthesis of benzochromene based dicyanoanilines, 13,30 as far as we know, this is the first general report on the synthesis of isochroman containing dicyanoanilines.…”
Section: Introductionmentioning
confidence: 99%
“…It should be noted that malononitrile is a very convenient reagent for many MCRs due to having a reactive methylene and two cyano groups to build several carbon-carbon and carbon-heteroatom bonds simoltaneously. 29 Thus, a pseudo four-component process takes place and a new series of dicyanoanilines 4 is obtained (Scheme 1). Although there is a few reports on the synthesis of benzochromene based dicyanoanilines, 13,30 as far as we know, this is the first general report on the synthesis of isochroman containing dicyanoanilines.…”
Section: Introductionmentioning
confidence: 99%
“…By minimizing the number of synthetic operations while maximizing the build-up of structural and functional complexities, these reactions are particularly appealing in the context of target-oriented synthesis (Mironovo, 2006;Shestopalov et al, 2008;Toure´and Hall, 2009;Zhang and Zhang, 2009;Zhu and Bienayme, 2005).…”
Section: Introductionmentioning
confidence: 99%
“…To the best of our knowledge, there are no reports in the literature for the formation of pyridazine derivatives via condensation of β-ketoesters with arylglyoxals in water. Currently, multicomponent reactions are being rapidly developed 20 because using a "onepot" methodology makes the synthesis simpler and more environmentally friendly. Additionally, the prospect of extending one-pot reactions into combinatorial and solid-phase syntheses 21,22 promises manifold opportunities for developing novel lead structures of pharmaceuticals, catalysts and even novel molecule-based materials.…”
Section: Introductionmentioning
confidence: 99%