Sateesh Dubbu

Affiliations: 
Indian Institute of Technology Kanpur, Kanpur, Uttar Pradesh, India 
Area:
Carbohydrate chemistry
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"Sateesh Dubbu"
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Publications

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Upadhyaya K, Dubbu S. (2024) Advancing carbohydrate functionality: The role of hypervalent iodine. Carbohydrate Research. 542: 109175
Kim S, Kumari N, Lim J, et al. (2021) Silica Jar-with-Lid as Chemo-Enzymatic Nano-Compartment for Enantioselective Synthesis inside Living Cells. Angewandte Chemie (International Ed. in English)
Lee J, Dubbu S, Kumari N, et al. (2020) Magnetothermia-Induced Catalytic Hollow Nanoreactor for Bioorthogonal Organic Synthesis in Living Cells. Nano Letters
Kumar A, Kumari N, Dubbu S, et al. (2020) Titelbild: Nanocatalosomes as Plasmonic Bilayer Shells with Interlayer Catalytic Nanospaces for Solar‐Light‐Induced Reactions (Angew. Chem. 24/2020) Angewandte Chemie. 132: 9281-9281
Dutta S, Kumari N, Dubbu S, et al. (2019) Highly Mesoporous Metal Organic Frameworks as Synergistic Multimodal Catalytic Platforms for Divergent Cascade Reactions. Angewandte Chemie (International Ed. in English)
Parasuraman K, Chennaiah A, Dubbu S, et al. (2019) Stereoselective synthesis of substituted 1,2-annulated sugars by domino double-Michael addition reaction. Carbohydrate Research. 477: 26-31
Verma AK, Dubbu S, Chennaiah A, et al. (2019) Synthesis of di- and trihydroxy proline derivatives from D-glycals: Application in the synthesis of polysubstituted pyrrolizidines and bioactive 1C-aryl/alkyl pyrrolidines. Carbohydrate Research. 475: 48-55
Verma AK, Chennaiah A, Dubbu S, et al. (2019) Palladium catalyzed synthesis of sugar-fused indolines via C(sp)-H/NH activation. Carbohydrate Research. 473: 57-65
Verma AK, Chennaiah A, Dubbu S, et al. (2018) Stereoselective synthesis of sugar-fused (or 1,2-annulated) isochromans and isochromanones by using oxa-Pictet-Spengler reaction. Organic & Biomolecular Chemistry
Dubbu S, Chennaiah A, Verma AK, et al. (2018) Stereoselective synthesis of 2-deoxy-β-C-aryl/alkyl glycosides using Prins cyclization: Application in the synthesis of C-disaccharides and differently protected C-aryl glycosides. Carbohydrate Research. 468: 64-68
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