Synthesis of New C2-Symmetric Six-Membered NHCs and Their Application for the Asymmetric Diethylzinc Addition of Arylaldehydes
A concise method for the preparation of new 3,4,5,6-tetrahydropyrimidinium salts was presented in this paper. Further application of these salts in asymmetric diethylzinc addition of arylaldehydes was explored, giving the corresponding chiral second alcohols in good yields and moderate enantioselect...
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doaj-95c49e86d0944adf9a198fe45e5299de2020-11-24T23:12:18ZengMDPI AGCatalysts2073-43442018-01-01824610.3390/catal8020046catal8020046Synthesis of New C2-Symmetric Six-Membered NHCs and Their Application for the Asymmetric Diethylzinc Addition of ArylaldehydesJie Li0Bihui Zhou1Yajie Jiang2Xiaoming Liu3School of Medicine, Zhejiang University City College, No. 48, Huzhou Road, Hangzhou 310015, ChinaSchool of Medicine, Zhejiang University City College, No. 48, Huzhou Road, Hangzhou 310015, ChinaSchool of Medicine, Zhejiang University City College, No. 48, Huzhou Road, Hangzhou 310015, ChinaDepartment of Dermatologry, The Third Affiliated Hospital of Soochow University, No. 185, Juqian Street, Changzhou 213000, ChinaA concise method for the preparation of new 3,4,5,6-tetrahydropyrimidinium salts was presented in this paper. Further application of these salts in asymmetric diethylzinc addition of arylaldehydes was explored, giving the corresponding chiral second alcohols in good yields and moderate enantioselectivities.http://www.mdpi.com/2073-4344/8/2/46N-heterocyclic carbenetetrahydropyrimidiniumenantioselectivityasymmetric additionchiral secondary alcohols |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jie Li Bihui Zhou Yajie Jiang Xiaoming Liu |
spellingShingle |
Jie Li Bihui Zhou Yajie Jiang Xiaoming Liu Synthesis of New C2-Symmetric Six-Membered NHCs and Their Application for the Asymmetric Diethylzinc Addition of Arylaldehydes Catalysts N-heterocyclic carbene tetrahydropyrimidinium enantioselectivity asymmetric addition chiral secondary alcohols |
author_facet |
Jie Li Bihui Zhou Yajie Jiang Xiaoming Liu |
author_sort |
Jie Li |
title |
Synthesis of New C2-Symmetric Six-Membered NHCs and Their Application for the Asymmetric Diethylzinc Addition of Arylaldehydes |
title_short |
Synthesis of New C2-Symmetric Six-Membered NHCs and Their Application for the Asymmetric Diethylzinc Addition of Arylaldehydes |
title_full |
Synthesis of New C2-Symmetric Six-Membered NHCs and Their Application for the Asymmetric Diethylzinc Addition of Arylaldehydes |
title_fullStr |
Synthesis of New C2-Symmetric Six-Membered NHCs and Their Application for the Asymmetric Diethylzinc Addition of Arylaldehydes |
title_full_unstemmed |
Synthesis of New C2-Symmetric Six-Membered NHCs and Their Application for the Asymmetric Diethylzinc Addition of Arylaldehydes |
title_sort |
synthesis of new c2-symmetric six-membered nhcs and their application for the asymmetric diethylzinc addition of arylaldehydes |
publisher |
MDPI AG |
series |
Catalysts |
issn |
2073-4344 |
publishDate |
2018-01-01 |
description |
A concise method for the preparation of new 3,4,5,6-tetrahydropyrimidinium salts was presented in this paper. Further application of these salts in asymmetric diethylzinc addition of arylaldehydes was explored, giving the corresponding chiral second alcohols in good yields and moderate enantioselectivities. |
topic |
N-heterocyclic carbene tetrahydropyrimidinium enantioselectivity asymmetric addition chiral secondary alcohols |
url |
http://www.mdpi.com/2073-4344/8/2/46 |
work_keys_str_mv |
AT jieli synthesisofnewc2symmetricsixmemberednhcsandtheirapplicationfortheasymmetricdiethylzincadditionofarylaldehydes AT bihuizhou synthesisofnewc2symmetricsixmemberednhcsandtheirapplicationfortheasymmetricdiethylzincadditionofarylaldehydes AT yajiejiang synthesisofnewc2symmetricsixmemberednhcsandtheirapplicationfortheasymmetricdiethylzincadditionofarylaldehydes AT xiaomingliu synthesisofnewc2symmetricsixmemberednhcsandtheirapplicationfortheasymmetricdiethylzincadditionofarylaldehydes |
_version_ |
1725601525989900288 |