Literature DB >> 33398642

Alkynoates as Versatile and Powerful Chemical Tools for the Rapid Assembly of Diverse Heterocycles under Transition-Metal Catalysis: Recent Developments and Challenges.

Imtiaz Khan1,2, Aliya Ibrar3, Sumera Zaib4.   

Abstract

Heterocycles, heteroaromatics and spirocyclic entities are ubiquitous components of a wide plethora of synthetic drugs, biologically active natural products, marketed pharmaceuticals and agrochemical targets. Recognizing their high proportion in drugs and rich pharmacological potential, these invaluable structural motifs have garnered significant interest, thus enabling the development of efficient catalytic methodologies providing access to architecturally complex and diverse molecules with high atom-economy and low cost. These chemical processes not only allow the formation of diverse heterocycles but also utilize a range of flexible and easily accessible building units in a single operation to discover diversity-oriented synthetic approaches. Alkynoates are significantly important, diverse and powerful building blocks in organic chemistry due to their unique and inherent properties such as the electronic bias on carbon-carbon triple bonds posed by electron-withdrawing groups or the metallic coordination site provided by carbonyl groups. The present review highlights the comprehensive picture of the utility of alkynoates (2007-2019) for the synthesis of various heterocycles (> 50 types) using transition-metal catalysts (Ru, Rh, Pd, Ir, Ag, Au, Pt, Cu, Mn, Fe) in various forms. The valuable function of versatile alkynoates (bearing multifunctional groups) as simple and useful starting materials is explored, thus cyclizing with an array of coupling partners to deliver a broad range of oxygen-, nitrogen-, sulfur-containing heterocycles alongside fused-, and spiro-heterocyclic compounds. In addition, these examples will also focus the scope and reaction limitations, as well as mechanistic investigations into the synthesis of these heterocycles. The biological significance will also be discussed, citing relevant examples of drug molecules highlighting each class of heterocycles. This review summarizes the recent developments in the synthetic methods for the synthesis of various heterocycles using alkynoates as readily available starting materials under transition-metal catalysis.

Entities:  

Keywords:  Alkynoates; Divergent reactivity; Heterocycles; Molecular complexity; Synthetic methods; Transition-metal catalysis

Mesh:

Substances:

Year:  2021        PMID: 33398642     DOI: 10.1007/s41061-020-00316-4

Source DB:  PubMed          Journal:  Top Curr Chem (Cham)        ISSN: 2364-8961


  484 in total

1.  Synthesis, crystal structure and biological evaluation of some novel 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazoles and 1,2,4-triazolo[3,4-b]-1,3,4-thiadiazines.

Authors:  Imtiaz Khan; Sumera Zaib; Aliya Ibrar; Nasim Hasan Rama; Jim Simpson; Jamshed Iqbal
Journal:  Eur J Med Chem       Date:  2014-03-19       Impact factor: 6.514

2.  Solvent-free heterocyclic synthesis.

Authors:  Marcos A P Martins; Clarissa P Frizzo; Dayse N Moreira; Lilian Buriol; Pablo Machado
Journal:  Chem Rev       Date:  2009-09       Impact factor: 60.622

3.  Chemistry of α-oxoesters: a powerful tool for the synthesis of heterocycles.

Authors:  Bagher Eftekhari-Sis; Maryam Zirak
Journal:  Chem Rev       Date:  2014-11-25       Impact factor: 60.622

4.  Arylglyoxals in synthesis of heterocyclic compounds.

Authors:  Bagher Eftekhari-Sis; Maryam Zirak; Ali Akbari
Journal:  Chem Rev       Date:  2013-01-25       Impact factor: 60.622

5.  Active compounds from a diverse library of triazolothiadiazole and triazolothiadiazine scaffolds: synthesis, crystal structure determination, cytotoxicity, cholinesterase inhibitory activity, and binding mode analysis.

Authors:  Imtiaz Khan; Aliya Ibrar; Sumera Zaib; Sarfraz Ahmad; Norbert Furtmann; Shahid Hameed; Jim Simpson; Jürgen Bajorath; Jamshed Iqbal
Journal:  Bioorg Med Chem       Date:  2014-09-06       Impact factor: 3.641

6.  A new entry into the portfolio of α-glucosidase inhibitors as potent therapeutics for type 2 diabetes: Design, bioevaluation and one-pot multi-component synthesis of diamine-bridged coumarinyl oxadiazole conjugates.

Authors:  Madiha Kazmi; Sumera Zaib; Aliya Ibrar; Sayyeda Tayyeba Amjad; Zainab Shafique; Saifullah Mehsud; Aamer Saeed; Jamshed Iqbal; Imtiaz Khan
Journal:  Bioorg Chem       Date:  2018-01-16       Impact factor: 5.275

7.  Exploration of aroyl/heteroaroyl iminothiazolines featuring 2,4,5-trichlorophenyl moiety as a new class of potent, selective, and in vitro efficacious glucosidase inhibitors.

Authors:  Madiha Kazmi; Sumera Zaib; Sayyeda Tayyeba Amjad; Imtiaz Khan; Aliya Ibrar; Aamer Saeed; Jamshed Iqbal
Journal:  Bioorg Chem       Date:  2017-07-25       Impact factor: 5.275

8.  Symmetrical aryl linked bis-iminothiazolidinones as new chemical entities for the inhibition of monoamine oxidases: Synthesis, in vitro biological evaluation and molecular modelling analysis.

Authors:  Naeem Abbas; Sumera Zaib; Syeda Mahwish Bakht; Aliya Ibrar; Imtiaz Khan; Sadaf Batool; Aamer Saeed; Jamshed Iqbal
Journal:  Bioorg Chem       Date:  2016-11-09       Impact factor: 5.275

Review 9.  Triazolothiadiazoles and triazolothiadiazines--biologically attractive scaffolds.

Authors:  Imtiaz Khan; Aliya Ibrar; Naeem Abbas
Journal:  Eur J Med Chem       Date:  2013-03-05       Impact factor: 6.514

10.  Exploration of thioxothiazolidinone-sulfonate conjugates as a new class of aldehyde/aldose reductase inhibitors: A synthetic and computational investigation.

Authors:  Hina Andleeb; Yildiz Tehseen; Farrukh Jabeen; Imtiaz Khan; Jamshed Iqbal; Shahid Hameed
Journal:  Bioorg Chem       Date:  2017-08-31       Impact factor: 5.275

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