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

96 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

Research Groups and Themes

BCS and TECS CDTs

Access to Document

10.1246/cl.150913

Handle.net

Persistent link

Embargoed Document

Full-text PDF (final published version)
Final published version, 1.65 MB

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

Cite this

@article{7574d4a3469d4407822c9bd0e9854185,

title = "Branch Selective Murai-Type Alkene Hydroarylation Reactions",

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.",

author = "Giacomo Crisenza and John Bower",

year = "2016",

month = jan,

doi = "10.1246/cl.150913",

language = "English",

volume = "45",

pages = "2--9",

journal = "Chemistry Letters",

issn = "0366-7022",

publisher = "Oxford University Press",

number = "1",

}

TY - JOUR

T1 - Branch Selective Murai-Type Alkene Hydroarylation Reactions

AU - Crisenza, Giacomo

AU - Bower, John

PY - 2016/1

Y1 - 2016/1

N2 - 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.

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.

U2 - 10.1246/cl.150913

DO - 10.1246/cl.150913

M3 - Article (Academic Journal)

SN - 0366-7022

VL - 45

SP - 2

EP - 9

JO - Chemistry Letters

JF - Chemistry Letters

IS - 1

ER -

Branch Selective Murai-Type Alkene Hydroarylation Reactions

Abstract

Research Groups and Themes

Access to Document

Handle.net

Embargoed Document

Fingerprint

Projects

3-month Core Capability for Chemistry Research

Cite this