Ajmal Khan

Prof. Dr. Ajmal Khan

orcid

Research Focus & Metrics

Academic Career Length

12Years (2015-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 September 2019 in Angewandte Chemie International Edition
Verified
Journal Article
Closed access
PDF file
AKAjmal Khan
Ajmal Khan
HZHeng Zhao
Heng Zhao
MZMeina Zhang
Meina Zhang
SKShahid Khan
Shahid Khan
DZDepeng Zhao
Depeng Zhao

28 July 2022 in Methods and Applications in Fluorescence
Verified
Journal Article
Open access
PDF file
Sami El DeebSami El Deeb
Sami El Deeb
Ahmed Al-HarrasiAhmed Al-Harrasi
Ahmed Al-Harrasi
AKAjmal Khan
Ajmal Khan
MAMohammed Al-Broumi
Mohammed Al-Broumi
GAGhanim Al-Thani
Ghanim Al-Thani
AIAdel Ibrahim
Adel Ibrahim
The in vitro panel of technologies to address biomolecular interactions are in play, however microscale thermophoresis is continuously increasing in use to represent a key player in this arena. This review highlights the usefulness of microscale thermophoresis in the determination of molecular and biomolecular affinity interactions. This work reviews the literature from January 2016 to January 2022 about microscale thermophoresis. It gives a summarized overview about both the state-of the art and the development in the field of microscale thermophoresis. The principle of microscale thermophoresis is also described supported with self-created illustrations. Moreover, some recent advances are mentioned that showing application of the technique in investigating biomolecular interactions in different fields. Finally, advantages as well as drawbacks of the technique in comparison with other competing techniques are summarized.

6 May 2020 in Chemical Science
Verified
Journal Article
Open access
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MSMuhammad Salman
Muhammad Salman
YXYaoyao Xu
Yaoyao Xu
SKShahid Khan
Shahid Khan
JZJunjie Zhang
Junjie Zhang
AKAjmal Khan
Ajmal Khan
The first molybdenum-catalyzed allylic sulfonylation of tertiary allylic electrophiles is described. The method employs a readily accessible catalyst (Mo(CO)6/2,2′-bipyridine, both are commercially available) and represents the first example of the use of a group 6 transition metal-catalyst for allylic sulfonylation of substituted tertiary allylic electrophiles to form carbon–sulfur bonds. This atom economic and operationally simple methodology is characterized by its relatively mild conditions, wide substrate scope, and excellent regioselectivity profile, thus unlocking a new platform to forge sulfone moieties, even in the context of late-stage functionalization and providing ample opportunities for further derivatization through traditional Suzuki cross-coupling reactions.

17 August 2020 in The Journal of Organic Chemistry
Verified
Journal Article
Closed access
YXYaoyao Xu
Yaoyao Xu
MSMuhammad Salman
Muhammad Salman
SKShahid Khan
Shahid Khan
JZJunjie Zhang
Junjie Zhang
AKAjmal Khan
Ajmal Khan

28 May 2020 in Green Chemistry
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Journal Article
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AKAjmal Khan
Ajmal Khan
JZJunjie Zhang
Junjie Zhang
SKShahid Khan
Shahid Khan
The development of green, economical and sustainable chemical processes is one of the primary challenges in organic chemistry. Herein, we report a recoverable heterogeneous palladium catalyst for the stereoselective synthesis of multi-functionalized allylic ethers under solvent free conditions. This method is based on in situ generated PdNP catalyzed O-allylation of alcohols with vinyl cyclic carbonates. Solvent-free conditions, easily recoverable catalysts, efficient recycling, and operational simplicity make the protocol green, economic and sustainable.

29 July 2023 in Organic Letters
Verified
Journal Article
Closed access
SKShahid Khan
Shahid Khan
JZJunjie Zhang
Junjie Zhang
AKAjmal Khan
Ajmal Khan