Catalytic enantioselective conjugate addition of grignard reagents to cyclic enones using C 1 -1,1′-bisisoquinoline-based chiral ligands

New highly constrained chiral C1-1,10-bisisoquinoline ligands were examined in the enantioselective conjugate addition of Grignard reagents to cyclohexenone and cyclopentenone. The desired 1,4-adducts were obtained in excellent yield and moderate enantiomeric excess (up to 35%).

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Main Authors: Judeh, Zaher M. A., Qi, Gao
Other Authors: School of Chemical and Biomedical Engineering
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/96144
http://hdl.handle.net/10220/11770
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-961442020-03-07T11:35:30Z Catalytic enantioselective conjugate addition of grignard reagents to cyclic enones using C 1 -1,1′-bisisoquinoline-based chiral ligands Judeh, Zaher M. A. Qi, Gao School of Chemical and Biomedical Engineering New highly constrained chiral C1-1,10-bisisoquinoline ligands were examined in the enantioselective conjugate addition of Grignard reagents to cyclohexenone and cyclopentenone. The desired 1,4-adducts were obtained in excellent yield and moderate enantiomeric excess (up to 35%). 2013-07-17T07:26:43Z 2019-12-06T19:26:18Z 2013-07-17T07:26:43Z 2019-12-06T19:26:18Z 2012 2012 Journal Article Qi, G., & Judeh, Z. M. A. (2012). Catalytic Enantioselective Conjugate Addition of Grignard Reagents to Cyclic Enones Using C 1 -1,1′-Bisisoquinoline-Based Chiral Ligands. Synthetic Communications: An International Journal for Rapid Communication of Synthetic Organic Chemistry, 42(11), 1585-1592. https://hdl.handle.net/10356/96144 http://hdl.handle.net/10220/11770 10.1080/00397911.2010.541969 en Synthetic communications: an international journal for rapid communication of synthetic organic chemistry © 2012 Taylor & Francis Group, LLC.
institution Nanyang Technological University
building NTU Library
country Singapore
collection DR-NTU
language English
description New highly constrained chiral C1-1,10-bisisoquinoline ligands were examined in the enantioselective conjugate addition of Grignard reagents to cyclohexenone and cyclopentenone. The desired 1,4-adducts were obtained in excellent yield and moderate enantiomeric excess (up to 35%).
author2 School of Chemical and Biomedical Engineering
author_facet School of Chemical and Biomedical Engineering
Judeh, Zaher M. A.
Qi, Gao
format Article
author Judeh, Zaher M. A.
Qi, Gao
spellingShingle Judeh, Zaher M. A.
Qi, Gao
Catalytic enantioselective conjugate addition of grignard reagents to cyclic enones using C 1 -1,1′-bisisoquinoline-based chiral ligands
author_sort Judeh, Zaher M. A.
title Catalytic enantioselective conjugate addition of grignard reagents to cyclic enones using C 1 -1,1′-bisisoquinoline-based chiral ligands
title_short Catalytic enantioselective conjugate addition of grignard reagents to cyclic enones using C 1 -1,1′-bisisoquinoline-based chiral ligands
title_full Catalytic enantioselective conjugate addition of grignard reagents to cyclic enones using C 1 -1,1′-bisisoquinoline-based chiral ligands
title_fullStr Catalytic enantioselective conjugate addition of grignard reagents to cyclic enones using C 1 -1,1′-bisisoquinoline-based chiral ligands
title_full_unstemmed Catalytic enantioselective conjugate addition of grignard reagents to cyclic enones using C 1 -1,1′-bisisoquinoline-based chiral ligands
title_sort catalytic enantioselective conjugate addition of grignard reagents to cyclic enones using c 1 -1,1′-bisisoquinoline-based chiral ligands
publishDate 2013
url https://hdl.handle.net/10356/96144
http://hdl.handle.net/10220/11770
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