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Indrapal Singh Aidhen
Researcher at Indian Institute of Technology Madras
Publications - 107
Citations - 982
Indrapal Singh Aidhen is an academic researcher from Indian Institute of Technology Madras. The author has contributed to research in topics: Aryl & Amide. The author has an hindex of 15, co-authored 104 publications receiving 836 citations. Previous affiliations of Indrapal Singh Aidhen include Savitribai Phule Pune University & University of California, Santa Cruz.
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Metal-free bipolar/octupolar organic dyes for DSSC application: A combined experimental and theoretical approach
Sudip Mandal,Suman Kushwaha,Ramesh Mukkamala,Vijaya K. Siripina,Indrapal Singh Aidhen,Balla Rajakumar,R. Kothandaraman +6 more
TL;DR: In this paper, the authors evaluated donorπ-linker acceptor (D-π-A) dyes experimentally, which either have 1 or 3 triphenylamine (TPA) donor in combination with either pyridine or N -methyl pyridinium ion ion as acceptor.
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New Reagent for Convenient Access to the α,β-Unsaturated N-Methoxy-N-methyl-amide Functionality by a Synthesis Based on the Julia Olefination Protocol†
TL;DR: In this paper, a new reagent for α,β-unsaturated N-methoxy-N-methyl-amide structural unit has been developed, which can be easily prepared in two convenient steps from 2-chloro-nmethoxide-n-methylacetamide, reacted with a variety of aldehydes under Julia conditions.
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Exploring the role of the spacers and acceptors on the triphenylamine-based dyes for dye-sensitized solar cells
Jagadeeswari Sivanadanam,Ramesh Mukkamala,Sudip Mandal,Raman Vedarajan,Noriyoshi Matsumi,Indrapal Singh Aidhen,Kothandaraman Ramanujam +6 more
TL;DR: In this article, six triphenylamine-based dyes were explored for their application in dye-sensitized solar cells (DSSCs), and the role of π-spacers, optical, electrochemical, and photovoltaic properties of the dyes are studied.
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Intramolecular arylation of soft carbon centre or enolate using Mn(III) acetate : Studies towards spirostructure of Fredericamycin A☆
TL;DR: In this paper, an intramolecular arylation of a cyclic β-diketone using Mn(OAc)3 was applied for construction of the spirocyclic structure in Fredericamycin A.
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A common building block for the syntheses of amorfrutin and cajaninstilbene acid libraries toward efficient binding with peroxisome proliferator-activated receptors
TL;DR: A common building block for the synthesis of amorfrutin and cajaninstilbene acid derivatives has been developed and the library of synthesized compounds has enabled identification of new nontoxic ligands of peroxisome proliferator-activated receptors (PPAR) and potential inhibitors of the transcriptional corepressor protein NCoR.