Enantioselective synthesis of trifluoromethylated tertiary thioethers through organocatalytic sulfa-Michael addition of thiols to β-trifluoromethyl β,β-disubstituted enones

Yao Feng Wang; Shaoxiang Wu; Pran Gopal Karmaker; Muhammad Sohail; Qi Wang; Fu Xue Chen

doi:10.1055/s-0034-1380138

Enantioselective synthesis of trifluoromethylated tertiary thioethers through organocatalytic sulfa-Michael addition of thiols to β-trifluoromethyl β,β-disubstituted enones

Yao Feng Wang
, Shaoxiang Wu
, Pran Gopal Karmaker
, Muhammad Sohail
, Qi Wang
, Fu Xue Chen^*

^*此作品的通讯作者

化学与化工学院

Beijing Institute of Technology
Nutrichem Company Limited Building D-1

科研成果: 期刊稿件 › 文章 › 同行评审

14 引用（Scopus）

摘要

An organocatalytic asymmetric sulfa-Michael addition of thiols to β-trifluoromethyl β,β-disubstituted (E)-enones in the presence of 10 mol% of a cinchona alkaloid-derived thiourea catalyst provides direct and simple access to chiral trifluoromethyl tertiary thioethers in high yields and up to 76% ee.

源语言	英语
页（从-至）	1147-1153
页数	7
期刊	Synthesis
卷	47
期	8
DOI	https://doi.org/10.1055/s-0034-1380138
出版状态	已出版 - 1 4月 2015

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@article{d3c3a81e62da463bb0e4e9a8a9ab9e15,

title = "Enantioselective synthesis of trifluoromethylated tertiary thioethers through organocatalytic sulfa-Michael addition of thiols to β-trifluoromethyl β,β-disubstituted enones",

abstract = "An organocatalytic asymmetric sulfa-Michael addition of thiols to β-trifluoromethyl β,β-disubstituted (E)-enones in the presence of 10 mol\% of a cinchona alkaloid-derived thiourea catalyst provides direct and simple access to chiral trifluoromethyl tertiary thioethers in high yields and up to 76\% ee.",

keywords = "Michael additions, asymmetric catalysis, enones, organocatalysis, sulfides, thiols",

author = "Wang, \{Yao Feng\} and Shaoxiang Wu and Karmaker, \{Pran Gopal\} and Muhammad Sohail and Qi Wang and Chen, \{Fu Xue\}",

note = "Publisher Copyright: {\textcopyright} Georg Thieme Verlag Stuttgart · New York.",

year = "2015",

month = apr,

day = "1",

doi = "10.1055/s-0034-1380138",

language = "English",

volume = "47",

pages = "1147--1153",

journal = "Synthesis",

issn = "0039-7881",

publisher = "Georg Thieme Verlag",

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TY - JOUR

T1 - Enantioselective synthesis of trifluoromethylated tertiary thioethers through organocatalytic sulfa-Michael addition of thiols to β-trifluoromethyl β,β-disubstituted enones

AU - Wang, Yao Feng

AU - Wu, Shaoxiang

AU - Karmaker, Pran Gopal

AU - Sohail, Muhammad

AU - Wang, Qi

AU - Chen, Fu Xue

N1 - Publisher Copyright: © Georg Thieme Verlag Stuttgart · New York.

PY - 2015/4/1

Y1 - 2015/4/1

N2 - An organocatalytic asymmetric sulfa-Michael addition of thiols to β-trifluoromethyl β,β-disubstituted (E)-enones in the presence of 10 mol% of a cinchona alkaloid-derived thiourea catalyst provides direct and simple access to chiral trifluoromethyl tertiary thioethers in high yields and up to 76% ee.

AB - An organocatalytic asymmetric sulfa-Michael addition of thiols to β-trifluoromethyl β,β-disubstituted (E)-enones in the presence of 10 mol% of a cinchona alkaloid-derived thiourea catalyst provides direct and simple access to chiral trifluoromethyl tertiary thioethers in high yields and up to 76% ee.

KW - Michael additions

KW - asymmetric catalysis

KW - enones

KW - organocatalysis

KW - sulfides

KW - thiols

UR - https://www.scopus.com/pages/publications/84926382730

U2 - 10.1055/s-0034-1380138

DO - 10.1055/s-0034-1380138

M3 - Article

AN - SCOPUS:84926382730

SN - 0039-7881

VL - 47

SP - 1147

EP - 1153

JO - Synthesis

JF - Synthesis

IS - 8

ER -

Enantioselective synthesis of trifluoromethylated tertiary thioethers through organocatalytic sulfa-Michael addition of thiols to β-trifluoromethyl β,β-disubstituted enones

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