Asymmetric ring-opening of oxabenzonorbornadiene with amines promoted by a chiral iridium-monophosphine catalyst

Renshi Luo; Jianhua Liao; Ling Xie; Wenjun Tang; Albert S.C. Chan

doi:10.1039/c3cc46009f

Asymmetric ring-opening of oxabenzonorbornadiene with amines promoted by a chiral iridium-monophosphine catalyst

Renshi Luo^*, Jianhua Liao, Ling Xie, Wenjun Tang^*, Albert S.C. Chan

^*Corresponding author for this work

Research output: Contribution to journal › Journal article › peer-review

43 Citations (Scopus)

Abstract

A new iridium-monophosphine catalyst is found to be efficient for asymmetric ring-opening of benzonorbornadiene with amines, providing a series of chiral substituted dihydronaphthalenes in high yields (up to 98%) and excellent enantioselectivities (>99%).

Original language	English
Pages (from-to)	9959-9961
Number of pages	3
Journal	Chemical Communications
Volume	49
Issue number	85
Early online date	2 Sept 2013
DOIs	https://doi.org/10.1039/c3cc46009f
Publication status	Published - 4 Nov 2013

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title = "Asymmetric ring-opening of oxabenzonorbornadiene with amines promoted by a chiral iridium-monophosphine catalyst",

abstract = "A new iridium-monophosphine catalyst is found to be efficient for asymmetric ring-opening of benzonorbornadiene with amines, providing a series of chiral substituted dihydronaphthalenes in high yields (up to 98%) and excellent enantioselectivities (>99%).",

author = "Renshi Luo and Jianhua Liao and Ling Xie and Wenjun Tang and Chan, {Albert S.C.}",

note = "Publisher copyright: {\textcopyright} The Royal Society of Chemistry 2013",

year = "2013",

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doi = "10.1039/c3cc46009f",

language = "English",

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T1 - Asymmetric ring-opening of oxabenzonorbornadiene with amines promoted by a chiral iridium-monophosphine catalyst

AU - Luo, Renshi

AU - Liao, Jianhua

AU - Xie, Ling

AU - Tang, Wenjun

AU - Chan, Albert S.C.

PY - 2013/11/4

Y1 - 2013/11/4

N2 - A new iridium-monophosphine catalyst is found to be efficient for asymmetric ring-opening of benzonorbornadiene with amines, providing a series of chiral substituted dihydronaphthalenes in high yields (up to 98%) and excellent enantioselectivities (>99%).

AB - A new iridium-monophosphine catalyst is found to be efficient for asymmetric ring-opening of benzonorbornadiene with amines, providing a series of chiral substituted dihydronaphthalenes in high yields (up to 98%) and excellent enantioselectivities (>99%).

UR - http://www.scopus.com/inward/record.url?scp=84885168355&partnerID=8YFLogxK

U2 - 10.1039/c3cc46009f

DO - 10.1039/c3cc46009f

M3 - Journal article

C2 - 24037423

AN - SCOPUS:84885168355

SN - 1359-7345

VL - 49

SP - 9959

EP - 9961

JO - Chemical Communications

JF - Chemical Communications

IS - 85

ER -

Asymmetric ring-opening of oxabenzonorbornadiene with amines promoted by a chiral iridium-monophosphine catalyst

Abstract

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