1 |
O15946Chemical Treatment of Electronic Waste: Challenges and Solutions (doi: https://doi.org/10.1007/978-981-97-8253-6_13) |
Waste Management for Smart Cities, Springer Nature Singapore Publisher |
eBook ISBN 978-981-97-8253-6 |
2025 |
2 |
O15964Photocatalysis: Application in Drug Derivatization (https://doi.org/10.1007/978-981-97-8205-5_6) |
Emerging Trends in Photoredox Synthetic Transformation, Springer Nature Singapore Publisher |
eBook ISBN 978-981-97-8205-5 |
2025 |
3 |
O15941Green Chemistry: The Emergence of a Transformative Framework (doi.org/10.1002/9781394212767.ch13) |
Sustainable Green Catalytic Processes, © 2024 Scrivener Publishing LLC |
293–318 |
2024 |
4 |
O15944N-Fluorobenzenesulfonimide (NFSI): A Multipurpose Reagent. (10.1007/978-981-97-5169-3_15) |
Emerging Trends in Synthesis and Catalysis in Chemistry. Conference Paper ETSC 2023. Springer Proceedings in Materials, Springer. |
51 |
2024 |
5 |
O15942N-Nitrosamide chemistry: Synthesis and applications in organic transformations (https://doi.org/10.1016/j.tetlet.2024.155154) |
Tetrahedron Letters |
145 |
2024 |
6 |
O15945Oxidative Coupling of N-Nitrosoanilines with Substituted Allyl Alcohols under Rhodium (III) Catalysis (doi: 10.3389/fchem.2024.1506493) |
Frontiers in Chemistry-Organic Section |
12 |
2024 |
7 |
O15940Synthesis of Environmental benign Biodiesel from Anabaena oil using Ba2SiO4 as efficient green catalyst (https://doi.org/10.1016/j.mcat.2024.113876) |
Molecular Catalysis |
556 |
2024 |
8 |
O15943Synthesis of Indazole Scaffolds from Arynes and Suitable Coupling Partners - A Brief Review (10.2174/0118756298321262240719103850) |
Mini-Reviews in Organic Chemistry |
21 |
2024 |
9 |
O15948Construction of Diverse Dihydrodibenzofuranones by Migration/Intramolecular Arylation of Iodonium Ylides |
Bulletin of the Korean Chemical Society |
42 |
2021 |
10 |
O15947In(III)‐Catalyzed O‐Annulation of Cyclic Diazodicarbonyls with 2‐Naphthol, 6‐ Quinolinol, β‐Tetralone, and 9‐Phenanthrol to Access Diverse Benzochromones |
Bulletin of the Korean Chemical Society |
42 |
2021 |
11 |
O15949Recent Advances and Strategies for the Transition-Metal Catalyzed C–H Functionalization of N-Nitrosoanilines |
Advanced Synthesis & Catalysis |
363 |
2021 |
12 |
O15950tert-Butyl nitrite catalyzed synthesis of benzimidazoles from o- phenylenediamine and aldehydes at room temperature |
Tetrahedron Letters |
61 (14) |
2020 |
13 |
O15952Copper-Promoted Dehydrogenative Cross- Coupling Reactions of Dialkyl Phosphites with Sulfoximines, |
Organic Chemistry Frontiers |
6 |
2019 |
14 |
O15954Regioselective nitration of N-alkyl anilines using tert-butyl nitrite under mild condition |
Journal of Organic Chemistry |
84(1) |
2019 |
15 |
O15953Synthesis of photolabile protecting group (PPG) protected uronic acid building blocks: applications in carbohydrate synthesis with the assistance of a continuous flow photoreactor |
Organic Chemistry Frontiers |
6 (23) |
2019 |
16 |
O15951tert- Butyl nitrite promoted transamidation of secondary amides under metal and catalyst free conditions |
Organic & Biomolecular Chemistry |
17 |
2019 |
17 |
O15955An Efficient Metal-Free Method for the Denitrosation of Aryl N-Nitrosamines at Room Temperature |
Advanced Synthesis & Catalysis |
360 (3) |
2018 |
18 |
O15958Potassium persulfate promoted N- nitrosation of secondary and tertiary amines with nitromethane under mild condition |
Asian Journal of Organic Chemistry |
7 |
2018 |
19 |
O15956tert-Butyl nitrite induced radical dimerization of primary thioamides and selenoamides at room temperature |
Tetrahedron Letters |
59 (3) |
2018 |
20 |
O15957tert-Butyl nitrite mediated nitrogen transfer reactions: Synthesis of benzotriazoles and azides at room temperature |
Organic & Biomolecular Chemistry |
16 |
2018 |
21 |
O15959Copper promoted N-alkylation of sulfoximines with alkyl boronic acid under mild conditions, Organic & Biomolecular Chemistry |
Organic & Biomolecular Chemistry |
15 (40) |
2017 |
22 |
O15960A chemoselective ipso-hydroxylation of arylboronic acids using urea-hydrogen peroxide under catalyst free condition |
Tetrahedron Letters |
57 (23) |
2016 |
23 |
O15962A metal free reduction of aryl-N- nitrosamines to the corresponding hydrazines using a sustainable reductant thiourea dioxide |
Green Chemistry |
18 (23) |
2016 |
24 |
O15961An efficient synthesis of N- nitrosamines under solvent, metal and acid free conditions using tert-butyl nitrite |
Green Chemistry |
18 (8) |
2016 |
25 |
O15963Bio-based green solvent for the catalyst free oxidation of arylboronic acids into phenols |
RSC Advances |
5 (108) |
2016 |