يعرض 1 - 10 نتائج من 37 نتيجة بحث عن '"Garima Jindal"', وقت الاستعلام: 0.88s تنقيح النتائج
  1. 1
    دورية أكاديمية
    A comparative evaluation of dermatoglyphics in different classes of malocclusion

    المؤلفون: Garima Jindal, Ramesh Kumar Pandey, Sameer Gupta, Meera Sandhu

    المصدر: Saudi Dental Journal, Vol 27, Iss 2, Pp 88-92 (2015)

    مصطلحات موضوعية: Medicine, Dentistry, RK1-715

    وصف الملف: electronic resource

    Relation: http://www.sciencedirect.com/science/article/pii/S1013905215000139; https://doaj.org/toc/1013-9052

    URL الوصول: https://doaj.org/article/a36114e5a4b143ddbdbf846ff6c65d24

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  2. 2
    The Role of Xantphos in forming an Elusive dirhodium-η1-allyl Intermediate in a Rh(II)-Catalyzed Allylic Alkylation: A Combined Computational and Experimental Study

    المؤلفون: Anubhav Goswami, Romin Gogoi, Arpita Panda, Aakash Chandresh Sheth, Garima Jindal

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::ae24ecee3bf9d1efd72f1dec5d384f90
    https://doi.org/10.26434/chemrxiv-2023-ksf8p

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  3. 3
    Revisiting the Burden Borne by Fumarase: Enzymatic Hydration of an Olefin

    المؤلفون: Asutosh Bellur, Soumik Das, Vijay Jayaraman, Sudarshan Behera, Arpitha Suryavanshi, Sundaram Balasubramanian, Padmanabhan Balaram, Garima Jindal, Hemalatha Balaram

    المصدر: Biochemistry.

    مصطلحات موضوعية: Biochemistry

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::690a06bb6a69c1af44ba0cf844af9f4c
    https://pubmed.ncbi.nlm.nih.gov/36595439

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  4. 4
    Aryne Three-Component Coupling Involving CS2 for the Synthesis of S-Aryl Dithiocarbamates

    المؤلفون: Garima Jindal, Subrata Bhattacharjee, Shiksha Deswal, Akkattu T. Biju, Niket Manoj

    المصدر: Organic Letters. 23:9083-9088

    مصطلحات موضوعية: Coupling (electronics), chemistry.chemical_compound, chemistry, Component (thermodynamics), Aryl, Organic Chemistry, Functional group, Density functional theory, Physical and Theoretical Chemistry, Biochemistry, Combinatorial chemistry, Aryne, Tetrahydrofuran

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::48cde98560992919324beb3be08d4ebd
    https://doi.org/10.1021/acs.orglett.1c03378

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  5. 5
    NHC‐Catalyzed Desymmetrization of N‐Aryl Maleimides Leading to the Atroposelective Synthesis of N‐Aryl Succinimides

    المؤلفون: Sayan Shee, Akkattu T. Biju, Garima Jindal, Subrata Mukherjee, Soumen Barik, Rajesh G. Gonnade, Soumik Das

    المصدر: Angewandte Chemie. 133:12372-12376

    مصطلحات موضوعية: 010405 organic chemistry, Chemistry, Aryl, Intermolecular force, Enantioselective synthesis, General Chemistry, General Medicine, 010402 general chemistry, 01 natural sciences, Medicinal chemistry, Desymmetrization, Catalysis, 0104 chemical sciences, Succinimides, chemistry.chemical_compound, Axial chirality, Organocatalysis

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::581148420c6cf6820d4f87138345b68e
    https://doi.org/10.1002/ange.202016938

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  6. 6
    Does an Enol Pathway Preclude High Stereoselectivity in Iron-Catalyzed Indole C-H Functionalization via Carbene Insertion?

    المؤلفون: Reena Balhara, Garima Jindal

    المصدر: The Journal of organic chemistry. 87(12)

    مصطلحات موضوعية: Indoles, Iron, Organic Chemistry, Protons, Methane, Catalysis

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8b2d29d8015c367d416e39d64f710d6
    https://pubmed.ncbi.nlm.nih.gov/35652604

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  7. 7
    Catalytic Enantioselective Desymmetrizing Fischer Indolization through Dynamic Kinetic Resolution

    المؤلفون: Biki Ghosh, Reena Balhara, Garima Jindal, Santanu Mukherjee

    المصدر: Angewandte Chemie International Edition. 60:9086-9092

    مصطلحات موضوعية: Indole test, Chemistry, Phenylhydrazines, Enantioselective synthesis, Organic chemistry, General Medicine, General Chemistry, Lewis acids and bases, Brønsted–Lowry acid–base theory, Desymmetrization, Catalysis, Kinetic resolution, Stereocenter

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a1f564cc93724b2f74a3e24de958b25f
    https://doi.org/10.1002/anie.202017268

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  8. 8
    DFT study on Ir-quinoid catalyzed C–H functionalization: new radical reactivity or direct carbene transfer?

    المؤلفون: Niket Manoj, Garima Jindal

    المصدر: Chemical Communications. 57:11370-11373

    مصطلحات موضوعية: Steric effects, Diene, Ligand, Metals and Alloys, General Chemistry, Hydrogen atom, Photochemistry, Catalysis, Surfaces, Coatings and Films, Electronic, Optical and Magnetic Materials, chemistry.chemical_compound, chemistry, Materials Chemistry, Ceramics and Composites, Reactivity (chemistry), Dehydrogenation, Carbene

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a52fc8b5b4838f53428ad6d116b1f28d
    https://doi.org/10.1039/d1cc04764g

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  9. 9
    N‐Heterocyclic Carbene‐Catalyzed Formal [6+2] Annulation Reaction via Cross‐Conjugated Aza‐Trienolate Intermediates

    المؤلفون: Akkattu T. Biju, Tatiana Besset, Arghya Ghosh, Kuruva Balanna, Thomas Poisson, Krishnaprasad Madica, Garima Jindal, Subrata Mukherjee

    المساهمون: Department of Theoretical and Applied Mechanics [Ithaca], Cornell University [New York], Chimie Organique et Bioorganique : Réactivité et Analyse (COBRA), Institut Normand de Chimie Moléculaire Médicinale et Macromoléculaire (INC3M), Institut de Chimie du CNRS (INC)-École Nationale Supérieure d'Ingénieurs de Caen (ENSICAEN), Normandie Université (NU)-Normandie Université (NU)-Institut national des sciences appliquées Rouen Normandie (INSA Rouen Normandie), Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Université Le Havre Normandie (ULH), Normandie Université (NU)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Centre National de la Recherche Scientifique (CNRS)-Université de Caen Normandie (UNICAEN), Normandie Université (NU)-Institut de Chimie du CNRS (INC)-École Nationale Supérieure d'Ingénieurs de Caen (ENSICAEN), Normandie Université (NU)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie Organique Fine (IRCOF), Université de Rouen Normandie (UNIROUEN), Institut National des Sciences Appliquées (INSA)-Normandie Université (NU)-Institut National des Sciences Appliquées (INSA)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS)

    المصدر: Chemistry-A European Journal
    Chemistry-A European Journal, Wiley-VCH Verlag, 2019, 26 (4), pp.818-822. ⟨10.1002/chem.201905177⟩

    مصطلحات موضوعية: Annulation, [CHIM.ORGA]Chemical Sciences/Organic chemistry, 010405 organic chemistry, Stereochemistry, Organic Chemistry, General Chemistry, Conjugated system, 010402 general chemistry, 01 natural sciences, Catalysis, 0104 chemical sciences, chemistry.chemical_compound, chemistry, Organocatalysis, Electrophile, [CHIM]Chemical Sciences, Reactivity (chemistry), Carbene

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f42fed8898509f13cbf1d732f3c1fb50
    https://doi.org/10.1002/chem.201905177

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  10. 10
    A computational approach to understand the role of metals and axial ligands in artificial heme enzyme catalyzed C-H insertion

    المؤلفون: Ritwika Chatterjee, Garima Jindal, Reena Balhara

    المصدر: Physical chemistry chemical physics : PCCP. 23(15)

    مصطلحات موضوعية: Archaeal Proteins, Iron, General Physics and Astronomy, Heme, Anisoles, 010402 general chemistry, Iridium, Ligands, 01 natural sciences, Catalysis, chemistry.chemical_compound, Cytochrome P-450 Enzyme System, Animals, Reactivity (chemistry), Benzopyrans, Physical and Theoretical Chemistry, Density Functional Theory, Sperm Whale, 010405 organic chemistry, Chemistry, Hydride, Ligand, Myoglobin, Rate-determining step, Porphyrin, 0104 chemical sciences, Crystallography, Catalytic cycle, Models, Chemical, Sulfolobaceae, Carbene, Azo Compounds, Oxidation-Reduction

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53c8fd0f066e17a6fbd4978304840743
    https://pubmed.ncbi.nlm.nih.gov/33885085

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