Literature DB >> 35423648

α-Aminoazoles/azines: key reaction partners for multicomponent reactions.

Shah Imtiaz1, Jahangir Ahmad War2, Syqa Banoo3, Sarfaraz Khan1.   

Abstract

Aromatic α-aminoazaheterocycles are the focus of significant investigations and exploration by researchers owing to their key role in diverse biological and physiological processes. The existence of their derivatives in numerous drugs and alkaloids is due to their heterocyclic nitrogenous nature. Therefore, the synthesis of a structurally diverse range of their derivatives through simple and convenient methods represents a vital field of synthetic organic chemistry. Multicomponent reactions (MCRs) provide a platform to introduce desirable structure diversity and complexity into a molecule in a single operation with a significant reduction in the use of harmful organic waste, and hence have attracted particular attention as an excellent tool to access these derivatives. This review covers the advances made from 2010 to the beginning of 2020 in terms of the utilization of α-aminoazaheterocycles as synthetic precursors in MCRs. This journal is © The Royal Society of Chemistry.

Entities:  

Year:  2021        PMID: 35423648      PMCID: PMC8695948          DOI: 10.1039/d1ra00392e

Source DB:  PubMed          Journal:  RSC Adv        ISSN: 2046-2069            Impact factor:   3.361


  70 in total

1.  Heterocycle-functional gramine analogues: solvent- and catalyst-free synthesis and their inhibition activities against cell proliferation.

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Journal:  Eur J Med Chem       Date:  2012-05-12       Impact factor: 6.514

2.  Synthesis and herbicidal activities of benzothiazole N,O-acetals.

Authors:  Zhiqin Ji; Fengxing Zhou; Shaopeng Wei
Journal:  Bioorg Med Chem Lett       Date:  2015-08-20       Impact factor: 2.823

3.  A green synthetic approach toward the synthesis of structurally diverse spirooxindole derivative libraries under catalyst-free conditions.

Authors:  Nazia Kausar; Abdulla Al Masum; Md Maidul Islam; Asish R Das
Journal:  Mol Divers       Date:  2017-02-11       Impact factor: 2.943

4.  Design and green synthesis of 2-(diarylalkyl)aminobenzothiazole derivatives and their dual activities as angiotensin converting enzyme inhibitors and calcium channel blockers.

Authors:  Praveen Kumar Kalavagunta; Pankaj K Bagul; Anvesh Jallapally; Srinivas Kantevari; Sanjay K Banerjee; Narender Ravirala
Journal:  Eur J Med Chem       Date:  2014-06-17       Impact factor: 6.514

5.  PEG-SO(3)H catalyzed synthesis and cytotoxicity of α-aminophosphonates.

Authors:  C Bhupendra Reddy; K Suresh Kumar; M Anil Kumar; M Veera Narayana Reddy; B Satheesh Krishna; M Naveen; M K Arunasree; C Suresh Reddy; C Naga Raju; C Devendranath Reddy
Journal:  Eur J Med Chem       Date:  2011-11-20       Impact factor: 6.514

Review 6.  Recent advances in the synthesis of pyrroles by multicomponent reactions.

Authors:  Verónica Estévez; Mercedes Villacampa; J Carlos Menéndez
Journal:  Chem Soc Rev       Date:  2014-07-07       Impact factor: 54.564

7.  A metal-free cyclic iminium induced one-pot double annulation cascade: access to dihydroisoquinolinium (DHIQ) salts.

Authors:  A Sagar; Venkata Nagarjuna Babu; Anand H Shinde; Duddu S Sharada
Journal:  Org Biomol Chem       Date:  2016-11-08       Impact factor: 3.876

8.  Sustainable three-component synthesis of isothioureas from isocyanides, thiosulfonates, and amines.

Authors:  Pieter Mampuys; Yanping Zhu; Tjøstil Vlaar; Eelco Ruijter; Romano V A Orru; Bert U W Maes
Journal:  Angew Chem Int Ed Engl       Date:  2014-09-15       Impact factor: 15.336

9.  An efficient three component one-pot synthesis of 5-amino-7-aryl-7,8-dihydro-[1,2,4] triazolo[4,3-a]-pyrimidine-6-carbonitriles.

Authors:  Keyume Ablajan; Wetengul Kamil; Anagu Tuoheti; Sun Wan-Fu
Journal:  Molecules       Date:  2012-02-14       Impact factor: 4.411

10.  One-pot synthesis of novel chiral β-amino acid derivatives by enantioselective Mannich reactions catalyzed by squaramide cinchona alkaloids.

Authors:  Kankan Zhang; Xueping Liang; Ming He; Jian Wu; Yuping Zhang; Wei Xue; Linhong Jin; Song Yang; Deyu Hu
Journal:  Molecules       Date:  2013-05-23       Impact factor: 4.411

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