2013
DOI: 10.1007/s11030-013-9430-5
|View full text |Cite
|
Sign up to set email alerts
|

A simple route for the synthesis of novel $$N$$ -alkyl-2-(alkylthio)-1 $$H$$ -imidazole derivatives

Abstract: Novel N-alkyl-2-(alkylthio)-1H-imidazole derivatives were synthesized in a single step by an efficient and simple method in high yields. Readily available starting materials, mild reaction conditions, operational simplicity and novelty are the key advantages of this method. Besides their novel structures, these compounds may have important biological activities and industrial applications.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3

Citation Types

0
3
0

Year Published

2015
2015
2022
2022

Publication Types

Select...
6

Relationship

3
3

Authors

Journals

citations
Cited by 6 publications
(3 citation statements)
references
References 19 publications
0
3
0
Order By: Relevance
“…Thus, the development of an eco-friendly and practical synthetic route for the efficient preparation of these pyridine derivatives will be a beneficial and interesting challenge. As part of our ongoing research program on the development of efficient methods for the preparation of biologically active compounds (43)(44)(45)(46)(47)(48), herein, we are going to report an efficient method for the synthesis of 2-amino-3-cyanopyridins under ultrasound waves. In this approach, the SBA-15@ADMPT/H 5 PW 10 V 2 O 40 was used as a highly efficient catalyst for the synthesis of highly substituted pyridines 3 via one-pot, four-component condensation reaction of aromatic aldehydes 1, cyclic ketones 2, ammonium acetate, and malononitrile at room temperature under ultrasound irradiation (Scheme 1).…”
Section: Introductionmentioning
confidence: 99%
“…Thus, the development of an eco-friendly and practical synthetic route for the efficient preparation of these pyridine derivatives will be a beneficial and interesting challenge. As part of our ongoing research program on the development of efficient methods for the preparation of biologically active compounds (43)(44)(45)(46)(47)(48), herein, we are going to report an efficient method for the synthesis of 2-amino-3-cyanopyridins under ultrasound waves. In this approach, the SBA-15@ADMPT/H 5 PW 10 V 2 O 40 was used as a highly efficient catalyst for the synthesis of highly substituted pyridines 3 via one-pot, four-component condensation reaction of aromatic aldehydes 1, cyclic ketones 2, ammonium acetate, and malononitrile at room temperature under ultrasound irradiation (Scheme 1).…”
Section: Introductionmentioning
confidence: 99%
“…As part of our current studies on the development of efficient methods for the preparation of biologically active compounds (36)(37)(38)(39)(40)(41)(42)(43)(44), in this paper, Fe 3 O 4 @SiO 2 @ADMPT/H 6 P 2 W 18 O 62 as a new inorganic-organic hybrid nanocatalyst was prepared, characterized, and used as an effective catalyst in the synthesis of 1,4-DHPs 4 via one-pot reaction of various aromatic aldehydes 1, ethyl acetoacetate 2, and ammonium acetate 3 with good to high yield in ethanol (Scheme 1). To the best of our knowledge, there are no examples of the use of WD HPAs as the catalyst for the synthesis of 1,4-DHP derivatives.…”
Section: Introductionmentioning
confidence: 99%
“…In modern organic chemistry, both tandem reactions and C-H functionalization are considered as efficient tools for the synthesis of complex molecules in terms of atom economy. As part of our ongoing research program on the development of efficient methods in organic synthesis and on the preparation of heterocyclic compounds [41][42][43][44][45][46], to develop a more atom economical and direct …”
Section: Introductionmentioning
confidence: 99%