Branch Selective Murai-Type Alkene Hydroarylation Reactions

Giacomo Crisenza; John Bower

doi:10.1246/cl.150913

Branch Selective Murai-Type Alkene Hydroarylation Reactions

Giacomo Crisenza, John Bower

Research output: Contribution to journal › Article (Academic Journal) › peer-review

91 Citations (Scopus)

Abstract

There is significant interest in the development of C–C bond-forming methodologies that directly access challenging benzylic stereocenters. Predominantly, efforts have been focused on the development of enantiospecific or enantioselective cross-coupling methodologies. An alternate and conceptually ideal approach involves the development of branch-selective and enantioselective Murai-type alkene hydroarylations. Recent progress towards this broad, yet challenging goal is highlighted.

Original language	English
Pages (from-to)	2-9
Number of pages	8
Journal	Chemistry Letters
Volume	45
Issue number	1
Early online date	5 Jan 2016
DOIs	https://doi.org/10.1246/cl.150913
Publication status	Published - Jan 2016

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3-month Core Capability for Chemistry Research
Crosby, J. (Principal Investigator)
1/01/13 → 1/04/13
Project: Research

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abstract = "There is significant interest in the development of C–C bond-forming methodologies that directly access challenging benzylic stereocenters. Predominantly, efforts have been focused on the development of enantiospecific or enantioselective cross-coupling methodologies. An alternate and conceptually ideal approach involves the development of branch-selective and enantioselective Murai-type alkene hydroarylations. Recent progress towards this broad, yet challenging goal is highlighted.",

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AB - There is significant interest in the development of C–C bond-forming methodologies that directly access challenging benzylic stereocenters. Predominantly, efforts have been focused on the development of enantiospecific or enantioselective cross-coupling methodologies. An alternate and conceptually ideal approach involves the development of branch-selective and enantioselective Murai-type alkene hydroarylations. Recent progress towards this broad, yet challenging goal is highlighted.

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DO - 10.1246/cl.150913

M3 - Article (Academic Journal)

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JF - Chemistry Letters

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Branch Selective Murai-Type Alkene Hydroarylation Reactions

Abstract

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3-month Core Capability for Chemistry Research

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