Year |
Citation |
Score |
2022 |
Ahmed J, Haug GC, Nguyen VD, Porey A, Trevino R, Larionov OV. Catalytic Dienylation: An Emergent Strategy for the Stereoselective Construction of Conjugated Dienes and Polyenes. Synthesis. 55: 1642-1651. PMID 37457884 DOI: 10.1055/a-1924-2564 |
0.615 |
|
2022 |
Ahmed J, Mandal SK. Phenalenyl Radical: Smallest Polycyclic Odd Alternant Hydrocarbon Present in the Graphene Sheet. Chemical Reviews. PMID 35561295 DOI: 10.1021/acs.chemrev.1c00963 |
0.555 |
|
2021 |
Banik A, Ahmed J, Sil S, Mandal SK. Mimicking transition metals in borrowing hydrogen from alcohols. Chemical Science. 12: 8353-8361. PMID 34221316 DOI: 10.1039/d1sc01681d |
0.813 |
|
2021 |
Singh B, Ahmed J, Biswas A, Paira R, Mandal SK. Reduced Phenalenyl in Catalytic Dehalogenative Deuteration and Hydrodehalogenation of Aryl Halides. The Journal of Organic Chemistry. PMID 33949861 DOI: 10.1021/acs.joc.1c00573 |
0.809 |
|
2021 |
Rajendran NM, Gautam N, Sarkar P, Ahmed J, Das A, Das S, Pati SK, Mandal SK. Bicyclic (alkyl)(amino)carbene stabilized zinc(0) complex with singlet biradicaloid ground state. Chemical Communications (Cambridge, England). PMID 33942839 DOI: 10.1039/d1cc01298c |
0.753 |
|
2020 |
Ahmed J, Datta P, Das A, Jomy S, Mandal SK. Switching between mono and doubly reduced odd alternant hydrocarbon: designing a redox catalyst. Chemical Science. 12: 3039-3049. PMID 34164073 DOI: 10.1039/d0sc05972b |
0.761 |
|
2020 |
Das A, Ahmed J, Rajendran NM, Adhikari D, Mandal SK. A Bottleable Imidazole-Based Radical as a Single Electron Transfer Reagent. The Journal of Organic Chemistry. PMID 33280378 DOI: 10.1021/acs.joc.0c02465 |
0.748 |
|
2020 |
Chakraborty S, Das A, Ahmed J, Barman S, Mandal SK. Designing a Cr-catalyst bearing redox non-innocent phenalenyl-based ligand towards hydrosilylative CO functionalization. Chemical Communications (Cambridge, England). PMID 33073795 DOI: 10.1039/d0cc05348a |
0.798 |
|
2020 |
Bhunia M, Sahoo SR, Das A, Ahmed J, Sreejyothi P, Mandal SK. Transition metal-free catalytic reduction of primary amides using an abnormal NHC based potassium complex: integrating nucleophilicity with Lewis acidic activation Chemical Science. 11: 1848-1854. DOI: 10.1039/C9Sc05953A |
0.81 |
|
2019 |
Bhunia M, Sahoo SR, Das A, Ahmed J, P S, Mandal SK. Transition metal-free catalytic reduction of primary amides using an abnormal NHC based potassium complex: integrating nucleophilicity with Lewis acidic activation. Chemical Science. 11: 1848-1854. PMID 34123278 DOI: 10.1039/c9sc05953a |
0.813 |
|
2019 |
Hota PK, Maji S, Ahmed J, Rajendran NM, Mandal SK. NHC-catalyzed silylative dehydration of primary amides to nitriles at room temperature. Chemical Communications (Cambridge, England). PMID 31830152 DOI: 10.1039/C9Cc08413D |
0.784 |
|
2019 |
Ahmed J, Swain AK, Das A, Govindarajan R, Bhunia M, Mandal SK. A K-arylacetylide complex for catalytic terminal alkyne functionalization using KOBu as a precatalyst. Chemical Communications (Cambridge, England). PMID 31670328 DOI: 10.1039/C9Cc07833A |
0.76 |
|
2019 |
Govindarajan R, Ahmed J, Swain AK, Mandal SK. Transition Metal-Free Catalytic Carboalkoxylation of Styrenes at Room Temperature. The Journal of Organic Chemistry. PMID 31533421 DOI: 10.1021/Acs.Joc.9B01744 |
0.691 |
|
2019 |
Das HS, Das S, Dey K, Singh B, K Haridasan R, Das A, Ahmed J, Mandal SK. Primary amides to amines or nitriles: a dual role by a single catalyst. Chemical Communications (Cambridge, England). PMID 31528894 DOI: 10.1039/C9Cc05856G |
0.787 |
|
2018 |
Vardhanapu PK, Ahmed J, Jose A, Shaw BK, Sen TK, Mathews AA, Mandal SK. Phenalenyl based Aluminum Compound for Catalytic C-H Arylation of Arene and Heteroarenes at Room Temperature. The Journal of Organic Chemistry. PMID 30507198 DOI: 10.1021/Acs.Joc.8B02699 |
0.741 |
|
2018 |
Ahmed J, Chakraborty S, Jose A, P S, Mandal SK. Integrating Organic Lewis Acid and Redox Catalysis: The Phenalenyl Cation in Dual Role. Journal of the American Chemical Society. PMID 29883115 DOI: 10.1021/Jacs.8B04786 |
0.792 |
|
2018 |
Vijaykumar G, Pariyar A, Ahmed J, Shaw BK, Adhikari D, Mandal SK. Tuning the redox non-innocence of a phenalenyl ligand toward efficient nickel-assisted catalytic hydrosilylation. Chemical Science. 9: 2817-2825. PMID 29732067 DOI: 10.1039/C7Sc04687A |
0.801 |
|
2017 |
Ahmed J, P S, Vijaykumar G, Jose A, Raj M, Mandal SK. A new face of phenalenyl-based radicals in the transition metal-free C-H arylation of heteroarenes at room temperature: trapping the radical initiator via C-C σ-bond formation. Chemical Science. 8: 7798-7806. PMID 29163916 DOI: 10.1039/C7Sc02661G |
0.785 |
|
2016 |
Paira R, Singh B, Hota PK, Ahmed J, Sau SC, Johnpeter JP, Mandal SK. Open-Shell Phenalenyl in Transition Metal-Free C-H Functionalization. The Journal of Organic Chemistry. PMID 26840833 DOI: 10.1021/Acs.Joc.6B00002 |
0.807 |
|
2016 |
Mandal SK, Ahmed J, Sau S, P S, Hota P, Vardhanapu P, Vijaykumar G. Direct C‐H Arylation of Heteroarenes with Aryl Chlorides using Abnormal NHC Coordinated Palladium Catalyst European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.201601218 |
0.795 |
|
2016 |
Paira R, Singh B, Hota PK, Ahmed J, Sau SC, Johnpeter JP, Mandal SK. ChemInform Abstract: Open-Shell Phenalenyl in Transition Metal-Free Catalytic C-H Functionalization. Cheminform. 47. DOI: 10.1002/CHIN.201631108 |
0.783 |
|
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