NaNO2/K2S2O8‐mediated Selective Radical Nitration/Nitrosation of Indoles: Efficient Approach to 3‐Nitro‐ and 3‐Nitrosoindoles

JPZ acknowledges financial support from the National Natural Science Foundation of China (No. 21172163, 21472133), the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), and Key Laboratory of Organic Synthesis of Jiangsu Province (KJS1749).

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Bibliographic Details
Published inAdvanced synthesis & catalysis Vol. 361; no. 10; pp. 2255 - 2261
Main Authors Shoberu, Adedamola, Li, Cheng‐Kun, Tao, Ze‐Kun, Zhang, Guo‐Yu, Zou, Jian‐Ping
Format Journal Article
LanguageEnglish
Published WEINHEIM Wiley 14.05.2019
Wiley Subscription Services, Inc
Subjects
Chemistry
Chemistry, Applied
Chemistry, Organic
C−H functionalization
Higher education institutions
Indole
Indoles
Nitration
Nitrosation
Physical Sciences
Potassium persulfate
Radical reaction
Science & Technology
Sodium nitrite
Nitration
Radical reaction
ENANTIOSELECTIVE SYNTHESIS
Indole
C-H functionalization
Nitrosation
N-OXIDES
CHEMOSELECTIVE NITRATION
C-H NITRATION
HETEROACENES BEARING
1,3-DIPOLAR CYCLOADDITION
CATALYZED NITRATION
NITROSO-COMPOUNDS
TERT-BUTYL NITRITE
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Summary:JPZ acknowledges financial support from the National Natural Science Foundation of China (No. 21172163, 21472133), the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD), and Key Laboratory of Organic Synthesis of Jiangsu Province (KJS1749).
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:1615-4150
1615-4169
DOI:10.1002/adsc.201900070