C−H Hydroxylation of Quinoxalin‐2(1H)‐ones throughipso‐Substitution Usingtert‐Butyl Nitrite
Author:
Affiliation:
1. School of Chemical Sciences National Institute of Science Education and Research (NISER), An OCC of Homi Bhaba National Institute, Bhubaneswar PO Bhimpur-Padanpur Via Jatni District Khurda, Odisha 752050 India
Funder
National Institute of Science Education and Research
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ejoc.202200425
Reference58 articles.
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2. tert ‐Butyl Nitrite (TBN), a Multitasking Reagent in Organic Synthesis
3. tert-Butyl Nitrite (TBN) as a Versatile Reagent in Organic Synthesis
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5. Regioselective C-7 Nitration of 8-Aminoquinoline Amides Using tert -Butyl Nitrite
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1. The Lacunae identified in processing, analyzing and finding means of catalyst free Oxone mediated through C-3 oxidation of N-alkyl quinoxalin-2(1 h )-one;Synthetic Communications;2024-03-18
2. Ionic liquid-catalysed regioselective oxygenation of quinoxalin-2(1H)-ones under visible-light conditions;New Journal of Chemistry;2023
3. Visible-Light Promoted Regioselective Oxygenation of Quinoxalin-2(1H)-ones Using O2 as an Oxidant;The Journal of Organic Chemistry;2022-10-10
4. Visible-Light-Induced Recyclable g-C3N4 Catalyzed C–H Hydroxylation of Quinoxalin-2(1H)-ones;Synthesis;2022-07-13
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