1,2-Aminothioethers Derived from Ephedrine and Pseudoephedrine: Heterobidentate Ligands for the Palladium-Catalysed Asymmetric Allylic Substitution Reaction
1
School of chemistry
Publication type: Journal Article
Publication date: 2002-12-18
scimago Q3
wos Q3
SJR: 0.437
CiteScore: 3.3
Impact factor: 1.4
ISSN: 09365214, 14372096
Organic Chemistry
Abstract
Heterobidentate sulfide-tertiary amine ligands incorporating 1,2-aminothioethers derived from ephedrine and pseudoephedrine have been prepared and used successfully in the palladium-catalysed asymmetric allylic substitution reaction, giving ees of up to 89%. The stereoelectronic effects operating in the reactions are discussed.
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Page P. 1,2-Aminothioethers Derived from Ephedrine and Pseudoephedrine: Heterobidentate Ligands for the Palladium-Catalysed Asymmetric Allylic Substitution Reaction // Synlett. 2002. Vol. 1. pp. 22-28.
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Page P. 1,2-Aminothioethers Derived from Ephedrine and Pseudoephedrine: Heterobidentate Ligands for the Palladium-Catalysed Asymmetric Allylic Substitution Reaction // Synlett. 2002. Vol. 1. pp. 22-28.
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TY - JOUR
DO - 10.1055/s-2003-36221
UR - https://doi.org/10.1055/s-2003-36221
TI - 1,2-Aminothioethers Derived from Ephedrine and Pseudoephedrine: Heterobidentate Ligands for the Palladium-Catalysed Asymmetric Allylic Substitution Reaction
T2 - Synlett
AU - Page, Philip
PY - 2002
DA - 2002/12/18
PB - Georg Thieme Verlag KG
SP - 22-28
IS - 1
SN - 0936-5214
SN - 1437-2096
ER -
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@article{2002_Page,
author = {Philip Page},
title = {1,2-Aminothioethers Derived from Ephedrine and Pseudoephedrine: Heterobidentate Ligands for the Palladium-Catalysed Asymmetric Allylic Substitution Reaction},
journal = {Synlett},
year = {2002},
publisher = {Georg Thieme Verlag KG},
month = {dec},
url = {https://doi.org/10.1055/s-2003-36221},
number = {1},
pages = {22--28},
doi = {10.1055/s-2003-36221}
}
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