Rhodium-catalyzed alkenyl C–H functionalization with amides
Literature Information
Publication Date
2019-05-10
DOI
10.1039/C9QO00489K
Impact Factor
5.281
Authors
Yao Huang, Wen-Jing Pan
View Original
Abstract
Rhodium-catalyzed pyridyl-directed alkenyl C–H bond functionalization with aroyl- or acryl-amides was carried out. The reaction gave arylated or alkenylated alkenes in moderate to excellent yields in most cases and tolerates functional groups involving RO, Cl, F, CF3, CN, COOMe, C(O)Me, and NO2.
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Source Journal
Organic Chemistry Frontiers
CiteScore:
7.8
Self-citation Rate:
8.7%
Articles per Year:
724
Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry
Recommended Compounds
N,N-Dimethyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2-pyrimidinamine
CAS Number:
1032759-30-0
Molecular Formula:
C12H20BN3O2
(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-phenylpropanoic acid
CAS Number:
1217663-60-9
Molecular Formula:
C24H21NO4
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