Enantioselective allylation of aldehydes catalyzed by chiral indium(III) complexes immobilized in ionic liquids

Jun Lu; Shun Jun Ji; Teck Peng Loh

doi:10.1039/b500086f

Enantioselective allylation of aldehydes catalyzed by chiral indium(III) complexes immobilized in ionic liquids

Jun Lu, Shun Jun Ji, Teck Peng Loh

科研成果: 期刊稿件 › 文章 › 同行评审

51 引用（Scopus）

摘要

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.

源语言	英语
页（从-至）	2345-2347
页数	3
期刊	Chemical Communications
期	18
DOI	https://doi.org/10.1039/b500086f
出版状态	已出版 - 14 5月 2005
已对外发布	是

访问文件

10.1039/b500086f

其它文件与链接

链接到 Scopus 的出版物

引用此

@article{d4cfb6795c2e4a03a6a61fff26e9d2ee,

title = "Enantioselective allylation of aldehydes catalyzed by chiral indium(III) complexes immobilized in ionic liquids",

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.",

author = "Jun Lu and Ji, {Shun Jun} and Loh, {Teck Peng}",

year = "2005",

month = may,

day = "14",

doi = "10.1039/b500086f",

language = "英语",

pages = "2345--2347",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "18",

}

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

PY - 2005/5/14

Y1 - 2005/5/14

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.

AB - 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.

UR - http://www.scopus.com/inward/record.url?scp=19944375130&partnerID=8YFLogxK

U2 - 10.1039/b500086f

DO - 10.1039/b500086f

M3 - 文章

C2 - 15877123

AN - SCOPUS:19944375130

SN - 1359-7345

SP - 2345

EP - 2347

JO - Chemical Communications

JF - Chemical Communications

IS - 18

ER -

Enantioselective allylation of aldehydes catalyzed by chiral indium(III) complexes immobilized in ionic liquids

摘要

访问文件

其它文件与链接

指纹

引用此