Highly diastereoselective synthesis of 3-hydroxy-2,2,3-trisubstituted indolines via intramolecular trapping of ammonium ylides with ketones

Changcheng Jing; Dong Xing; Wenhao Hu

doi:10.1039/c3cc48067d

Highly diastereoselective synthesis of 3-hydroxy-2,2,3-trisubstituted indolines via intramolecular trapping of ammonium ylides with ketones

Changcheng Jing
, Dong Xing
, Wenhao Hu^*

^*此作品的通讯作者

化学与分子工程学院

East China Normal University

科研成果: 期刊稿件 › 文章 › 同行评审

42 引用（Scopus）

摘要

A Rh₂(OAc)₄-catalyzed diazo decomposition reaction of diazo esters with 2-aminophenyl ketones is reported. A series of 3-hydroxy-2,2,3-trisubstituted indolines are produced in good yields with excellent diastereoselectivities via an intramolecular aldol-type trapping of ammonium ylides with ketone units.

源语言	英语
页（从-至）	951-953
页数	3
期刊	Chemical Communications
卷	50
期	8
DOI	https://doi.org/10.1039/c3cc48067d
出版状态	已出版 - 19 12月 2014

访问文件

10.1039/c3cc48067d

其它文件与链接

链接到 Scopus 的出版物

引用此

@article{0e6a8ced71194f45ad61ae91c3809ed5,

title = "Highly diastereoselective synthesis of 3-hydroxy-2,2,3-trisubstituted indolines via intramolecular trapping of ammonium ylides with ketones",

abstract = "A Rh2(OAc)4-catalyzed diazo decomposition reaction of diazo esters with 2-aminophenyl ketones is reported. A series of 3-hydroxy-2,2,3-trisubstituted indolines are produced in good yields with excellent diastereoselectivities via an intramolecular aldol-type trapping of ammonium ylides with ketone units.",

author = "Changcheng Jing and Dong Xing and Wenhao Hu",

year = "2014",

month = dec,

day = "19",

doi = "10.1039/c3cc48067d",

language = "英语",

volume = "50",

pages = "951--953",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "8",

}

TY - JOUR

T1 - Highly diastereoselective synthesis of 3-hydroxy-2,2,3-trisubstituted indolines via intramolecular trapping of ammonium ylides with ketones

AU - Jing, Changcheng

AU - Xing, Dong

AU - Hu, Wenhao

PY - 2014/12/19

Y1 - 2014/12/19

N2 - A Rh2(OAc)4-catalyzed diazo decomposition reaction of diazo esters with 2-aminophenyl ketones is reported. A series of 3-hydroxy-2,2,3-trisubstituted indolines are produced in good yields with excellent diastereoselectivities via an intramolecular aldol-type trapping of ammonium ylides with ketone units.

AB - A Rh2(OAc)4-catalyzed diazo decomposition reaction of diazo esters with 2-aminophenyl ketones is reported. A series of 3-hydroxy-2,2,3-trisubstituted indolines are produced in good yields with excellent diastereoselectivities via an intramolecular aldol-type trapping of ammonium ylides with ketone units.

UR - https://www.scopus.com/pages/publications/84890854942

U2 - 10.1039/c3cc48067d

DO - 10.1039/c3cc48067d

M3 - 文章

C2 - 24302029

AN - SCOPUS:84890854942

SN - 1359-7345

VL - 50

SP - 951

EP - 953

JO - Chemical Communications

JF - Chemical Communications

IS - 8

ER -

Highly diastereoselective synthesis of 3-hydroxy-2,2,3-trisubstituted indolines via intramolecular trapping of ammonium ylides with ketones

摘要

访问文件

其它文件与链接

学术指纹

引用此