The direct decarboxylative allylation of N-arylglycine derivatives by photoredox catalysis
Literature Information
Publication Date
2016-12-26
DOI
10.1039/C6QO00711B
Impact Factor
5.281
Authors
Yingqian Duan, Muliang Zhang, Rehanguli Ruzi, Zhongkai Wu
View Original
Abstract
The direct decarboxylative allylation of N-arylglycine derivatives has been accomplished via visible-light photoredox catalysis. With the substrates of N-aryl glycine derivatives and allylsulfone, a series of allylation products by a redox-neutral process were readily synthesized in good yields under mild conditions. The further utility of this allylation reaction has also been evaluated for valuable structural motifs.
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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
5,10,15,20-tetrakis(4-boronic acid pinacol ester phenyl) porphyrin
CAS Number:
1332748-00-1
Molecular Formula:
C68H74B4N4O8
![6,7-Dihydro-5H-pyrrolo[1,2-a]imidazole-6-carboxylic acid structure](https://static.chemtradehub.com/structs/136/1369160-12-2-6524.webp "6,7-Dihydro-5H-pyrrolo[1,2-a]imidazole-6-carboxylic acid structure")
6,7-Dihydro-5H-pyrrolo[1,2-a]imidazole-6-carboxylic acid
CAS Number:
1369160-12-2
Molecular Formula:
C7H8N2O2
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