Photocatalytic borylcyclopropanation of α-boryl styrenes

Literature Information

Publication Date 2019-03-20
DOI 10.1039/C9QO00197B
Impact Factor 5.281
Authors

Tsuyoshi Ohtani, Yuto Tsuchiya, Daisuke Uraguchi


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Abstract

A diastereoselective borylcyclopropanation of α-MIDA-boryl styrenes with 1,1-diiodoborylmethane is developed using 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyanobenzene (4CzIPN) as a catalyst under visible-light irradiation. The scope of this photocatalytic method is explored, and the utility of the resulting doubly borylated cyclopropanes is demonstrated by the selective transformation of one of the two boryl groups.

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Contents list

2021-02-24 Front/Back Matter

DOI: 10.1039/C2PY90010F

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Organic Chemistry Frontiers

Organic Chemistry Frontiers
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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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