Enantioselective allylation of aldehydes catalyzed by chiral indium(III) complexes immobilized in ionic liquids.Chem Commun (Camb). 2005 May 14CC
Abstract
In the presence of chiral catalytic complexes prepared from In(OTf)3 and chiral PYBOX ligands, allytributylstannane reacted with aldehydes in ionic liquids to afford the corresponding homoallylic alcohols in high enantioselectivities (86-94% ee) and good yields (68-89%); the chiral catalysts immobilized in ionic liquids could be reused with comparable enantioselectivities and yields.
Links
MeSH
Pub Type(s)
Journal Article
Research Support, Non-U.S. Gov't
Language
eng
PubMed ID
15877123
Citation
Lu, Jun, et al. "Enantioselective Allylation of Aldehydes Catalyzed By Chiral indium(III) Complexes Immobilized in Ionic Liquids." Chemical Communications (Cambridge, England), 2005, pp. 2345-7.
Lu J, Ji SJ, Loh TP. Enantioselective allylation of aldehydes catalyzed by chiral indium(III) complexes immobilized in ionic liquids. Chem Commun (Camb). 2005.
Lu, J., Ji, S. J., & Loh, T. P. (2005). Enantioselective allylation of aldehydes catalyzed by chiral indium(III) complexes immobilized in ionic liquids. Chemical Communications (Cambridge, England), (18), 2345-7.
Lu J, Ji SJ, Loh TP. Enantioselective Allylation of Aldehydes Catalyzed By Chiral indium(III) Complexes Immobilized in Ionic Liquids. Chem Commun (Camb). 2005 May 14;(18)2345-7. PubMed PMID: 15877123.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - Enantioselective allylation of aldehydes catalyzed by chiral indium(III) complexes immobilized in ionic liquids.
AU - Lu,Jun,
AU - Ji,Shun-Jun,
AU - Loh,Teck-Peng,
Y1 - 2005/03/15/
PY - 2005/5/7/pubmed
PY - 2007/3/14/medline
PY - 2005/5/7/entrez
SP - 2345
EP - 7
JF - Chemical communications (Cambridge, England)
JO - Chem Commun (Camb)
IS - 18
N2 - In the presence of chiral catalytic complexes prepared from In(OTf)3 and chiral PYBOX ligands, allytributylstannane reacted with aldehydes in ionic liquids to afford the corresponding homoallylic alcohols in high enantioselectivities (86-94% ee) and good yields (68-89%); the chiral catalysts immobilized in ionic liquids could be reused with comparable enantioselectivities and yields.
SN - 1359-7345
UR - https://www.unboundmedicine.com/medline/citation/15877123/Enantioselective_allylation_of_aldehydes_catalyzed_by_chiral_indium_III__complexes_immobilized_in_ionic_liquids_
L2 - https://doi.org/10.1039/b500086f
DB - PRIME
DP - Unbound Medicine
ER -