Negar Lashgari
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Negar Lashgari has a total of 37 co-authors. Here are the top co-authors by number of shared publications:
- Ghodsi Mohammadi Ziarani
Department of Organic Chemistry, Faculty of Chemistry, Alzahra University, Tehran, Iran
56 shared publications - Alireza Badiei
School of Chemistry, College of Science University of Tehran Tehran Iran
36 shared publications - Razieh Moradi
Department of Chemistry, Alzahra University, Tehran, Iran
8 shared publications Parisa Gholamzadeh
Department of Chemistry, Alzahra University, Vanak Square, P.O. Box 1993893973, Tehran, Iran
7 shared publications- Hendrik Gerhardus Kruger
University of KwaZulu-Natal
5 shared publications Jafar Afshani
School of Chemistry, College of Science University of Tehran Tehran Iran
5 shared publications
Latest Publications
- Open Access
- 13 August 2019
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 9 (43) , 25094-25106
The role of hollow magnetic nanoparticles in drug delivery
The increasing number of scientific publications focusing on nanomaterials in the biomedical field indicates growing interest from the broader scientific community.
- 13 August 2019
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 9 (43) , 25094-25106
Open AccessThe role of hollow magnetic nanoparticles in drug delivery
The increasing number of scientific publications focusing on nanomaterials in the biomedical field indicates growing interest from the broader scientific community.
- 1 July 2018
- Published by Elsevier in Bioorganic & Medicinal Chemistry
- Vol. 26 (12) , 3076-3095
Design, synthesis and biological evaluation of benzofuran appended benzothiazepine derivatives as inhibitors of butyrylcholinesterase and antimicrobial agents
- 1 July 2018
- Published by Elsevier in Bioorganic & Medicinal Chemistry
- Vol. 26 (12) , 3076-3095
Design, synthesis and biological evaluation of benzofuran appended benzothiazepine derivatives as inhibitors of butyrylcholinesterase and antimicrobial agents
- Open Access
- 28 March 2018
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 8 (22) , 12069-12103
Recent advances in the application of indoles in multicomponent reactions
An overview on recent applications of indoles in multicomponent reactions for the synthesis of heterocyclic compounds is provided.
- 28 March 2018
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 8 (22) , 12069-12103
Open AccessRecent advances in the application of indoles in multicomponent reactions
An overview on recent applications of indoles in multicomponent reactions for the synthesis of heterocyclic compounds is provided.
- Open Access
- 1 March 2018
- Vol. 17 (2) , 525-534
Efficient Synthesis and Antimicrobial Evaluation of Pyrazolopyranopyrimidines in the Presence of SBA-Pr-SO3H as a Nanoporous Acid Catalyst
A simple, efficient, and environmentally friendly method has been developed for the synthesis of a series of tricyclic fused pyrazolopyranopyrimidines via a one-pot three-component reaction of barbituric acids, aromatic aldehydes, and 3-methyl-5-pyrazolone in the presence of SBA-Pr-SO3H. SBA-15 mesoporous silica material functionalized with propyl sulfonic acid groups was used as a heterogeneous Bronsted acid catalyst with hexagonal structure, high surface area, thick walls, and large uniform pores. All reactions were performed under reflux conditions in water in the presence of a catalytic amount of SBA-Pr-SO3H. High yields, mild reaction conditions, short reaction times, and simple work-up procedures are some advantages of this method. The antimicrobial activities of the synthesized compounds were also evaluated and some products exhibited significant antibacterial activities at low concentrations.
- 1 March 2018
- Vol. 17 (2) , 525-534
Open AccessEfficient Synthesis and Antimicrobial Evaluation of Pyrazolopyranopyrimidines in the Presence of SBA-Pr-SO3H as a Nanoporous Acid Catalyst
A simple, efficient, and environmentally friendly method has been developed for the synthesis of a series of tricyclic fused pyrazolopyranopyrimidines via a one-pot three-component reaction of barbituric acids, aromatic aldehydes, and 3-methyl-5-pyrazolone in the presence of SBA-Pr-SO3H. SBA-15 mesoporous silica material functionalized with propyl sulfonic acid groups was used as a heterogeneous Bronsted acid catalyst with hexagonal structure, high surface area, thick walls, and large uniform pores. All reactions were performed under reflux conditions in water in the presence of a catalytic amount of SBA-Pr-SO3H. High yields, mild reaction conditions, short reaction times, and simple work-up procedures are some advantages of this method. The antimicrobial activities of the synthesized compounds were also evaluated and some products exhibited significant antibacterial activities at low concentrations.
- 1 March 2018
- Published by Elsevier in Tetrahedron
- Vol. 74 (13) , 1323-1353
Asymmetric synthesis of chiral oxindoles using isatin as starting material
- 1 March 2018
- Published by Elsevier in Tetrahedron
- Vol. 74 (13) , 1323-1353
Asymmetric synthesis of chiral oxindoles using isatin as starting material
- 1 January 2018
- Published by CLOCKSS Archive in HETEROCYCLES
- Vol. 96 (3) , 381-424
4-Hydroxy-6-methyl-2-pyrone: A Versatile Synthon in the Synthesis of Heterocyclic Scaffolds via Multicomponent Reactions
- 1 January 2018
- Published by CLOCKSS Archive in HETEROCYCLES
- Vol. 96 (3) , 381-424
4-Hydroxy-6-methyl-2-pyrone: A Versatile Synthon in the Synthesis of Heterocyclic Scaffolds via Multicomponent Reactions