2015
DOI: 10.1007/s11030-015-9622-2
|View full text |Cite
|
Sign up to set email alerts
|

Combined isocyanide-based multi-component Ullmann-type reaction: an efficient access to novel nitrogen-containing pentacyclic compounds

Abstract: 2-Chloro-3-formyl quinoline has been applied as an aldehyde moiety in the Groebke-Blackburn-Bienaymé multi-component reaction with isocyanides, 2-aminoazines, and 2-aminoazole to afford the desired adducts which are amenable for further cyclization on the basis of Ullmann-type coupling. The copper iodide-mediated intramolecular C-N bond formation in the second step gave an easy access to a series of imidazo[4[Formula: see text],5[Formula: see text]:4,5]pyrrolo[2,3-b]quinoline derivatives in moderate to good yi… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

0
10
0

Year Published

2016
2016
2020
2020

Publication Types

Select...
7
1

Relationship

1
7

Authors

Journals

citations
Cited by 19 publications
(10 citation statements)
references
References 42 publications
(45 reference statements)
0
10
0
Order By: Relevance
“…B: the proposed mechanism, driven by the stability of the product and properties of the initial starting material, such as aromaticity of the ring, bulkiness of substituents and solvent. No solvent [19,60,71,79,81,83,85,90,92,93,101,105,111,112,127,133,140,147,148,161,172,192,195] 23 Water [46,76] 2 Toluene [43,49,52,70,95,109,144,145,158,159,163,164,171,186,189,190] 17 DMSO [33,36] 2 EtOH [57,84,89,104,113,115,116,<...>…”
Section: Solvents Used In the Gbb-3crmentioning
confidence: 99%
“…B: the proposed mechanism, driven by the stability of the product and properties of the initial starting material, such as aromaticity of the ring, bulkiness of substituents and solvent. No solvent [19,60,71,79,81,83,85,90,92,93,101,105,111,112,127,133,140,147,148,161,172,192,195] 23 Water [46,76] 2 Toluene [43,49,52,70,95,109,144,145,158,159,163,164,171,186,189,190] 17 DMSO [33,36] 2 EtOH [57,84,89,104,113,115,116,<...>…”
Section: Solvents Used In the Gbb-3crmentioning
confidence: 99%
“…Foroumadi and co-workers reported in 2015 the synthesis of imidazo[1,2-a]pyridine in moderate yields (82-93%) via a GBBR using NH4Cl in stoichiometric quantities and hard conditions (Scheme 1) [17]. Our methodology has some advantages, for example, the synthetic process worked well under green catalyst.…”
Section: Introductionmentioning
confidence: 85%
“…Alireza Foroumadi et al (in 2015) synthesized imidazo[1,2-a] pyridine or imidazo[2,1-b]thiazole bound quinolones 40 [53] via GBBR. The reaction of 2-chloro-3-formyl quinolone with 2aminoazines or 2-aminoazoles and isocyanides in the presence of NH 4 Cl catalyst in toluene solvent at reflux temperature afforded the products in 65-93 % yield (Scheme 21i).…”
Section: Gbbr Based Imcrs For the Synthesis Of Bound Type Bhcsmentioning
confidence: 99%