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Felicia Phei Lin Lim

Researcher at Monash University Malaysia Campus

Publications -  39
Citations -  356

Felicia Phei Lin Lim is an academic researcher from Monash University Malaysia Campus. The author has contributed to research in topics: Triethyl orthoformate & Cyanamide. The author has an hindex of 9, co-authored 35 publications receiving 247 citations. Previous affiliations of Felicia Phei Lin Lim include Curtin University & Monash University.

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1,3,5-Triazine-based analogues of purine: from isosteres to privileged scaffolds in medicinal chemistry

TL;DR: Application of the isosterism concept for the development of new compounds with therapeutic potential in areas involving purinergic regulation or purine metabolism led to significant advances in medicinal chemistry of the azolo[1,3,5]triazines.
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A one-pot, three-component aminotriazine annulation onto 5-aminopyrazole-4-carbonitriles under microwave irradiation

TL;DR: In this article, a one-pot, three-component, microwave assisted reaction of 5-aminopyrazole-4-carbonitriles, triethyl orthoformate and cyanamide afforded novel 7-arylamino-substituted 4-amina-addicted 8-carbonite.
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A one-pot, three-component, microwave-assisted synthesis of novel 7-amino-substituted 4-aminopyrazolo[1,5-a][1,3,5]triazine-8-carbonitriles

TL;DR: In this article, a three-component reaction of 3-amino-substituted 5-aminopyrazole-4-carbonitriles, cyanamide and triethyl orthoformate under microwave irradiation was used for the synthesis of pyrazolo.
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A new, one-pot, multicomponent synthesis of 5-aza-9-deaza-adenines under microwave irradiation ☆

TL;DR: In this article, a three-component method for the synthesis of 5-aza-9-deaza-adenines was developed, where Aminopyrazoles react in a one-pot fashion with triethyl orthoformate and cyanamide under microwave irradiation.
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A multicomponent reaction of 2-aminoimidazoles: microwave-assisted synthesis of novel 5-aza-7-deaza-adenines

TL;DR: An efficient and highly selective multicomponent synthesis of 4-aminoimidazo[1,2-a][1,3,5]triazines, which are 5-aza-7-deaza-isosteres of adenine, was developed and a rearrangement was proposed to explain the high selectivity of the reaction.