tert-Butyl peroxybenzoate mediated formation of 3-alkylated quinolines from N-propargylamines via a cascade radical addition/cyclization reaction
Literature Information
Publication Date
2017-12-01
DOI
10.1039/C7QO01052D
Impact Factor
5.281
Authors
Wei Chen, Pinhua Li
View Original
Abstract
A tert-butyl peroxybenzoate (TBPB) mediated direct functionalization of N-propargyl aromatic amine derivatives with ethers has been developed. This procedure provides a new strategy toward the synthesis of 3-alkylated quinolines in one step via a domino radical addition/cyclization reaction under metal-free conditions.
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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
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{[3-(Hexadecyloxy)propoxy](hydroxy)phosphoryl}methyl 4-methylbenzenesulfonate
CAS Number:
864068-45-1
Molecular Formula:
C27H49O7PS
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CAS Number:
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Molecular Formula:
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