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ID 52538
File
language
eng
Author
Watanabe, Mirai Department of Chemistry, Graduate School of Natural Science and Technology, Shimane University, 1060 Nishikawatsu, Matsue, 690-8504 Japan
Sakai, Takuya Department of Chemistry, Graduate School of Natural Science and Technology, Shimane University, 1060 Nishikawatsu, Matsue, 690-8504 Japan
Oka, Marina Department of Chemistry, Graduate School of Natural Science and Technology, Shimane University, 1060 Nishikawatsu, Matsue, 690-8504 Japan
Makinose, Yuki Department of Chemistry, Graduate School of Natural Science and Technology, Shimane University, 1060 Nishikawatsu, Matsue, 690-8504 Japan
Miyazaki , Hidetoshi Department of Chemistry, Graduate School of Natural Science and Technology, Shimane University, 1060 Nishikawatsu, Matsue, 690-8504 Japan
Description
A heterogeneous chiral imidazolodinone catalyst was synthesized by immobilization on a sulfated
chitin through non-covalent ionic interactions. The chitin-based organocatalyst promoted the asymmetric Diels-Alder reaction with high enantioselectivity under heterogeneous conditions and was successfully reused multiple times without apparent loss of catalytic activity and enantioselectivity.
Subject
Organocatalysis
heterogeneous catalysis
asymmetric Diels-Alder reaction
imidazolidinone
chitin
Journal Title
Advanced Synthesis & Catalysis
Volume
162
Issue
1
ISSN
1615-4169
Published Date
2019-11-12
DOI
Publisher
Wiley
NII Type
Journal Article
Format
PDF
Relation
Rights
This is the peer reviewed version of the following article: https://onlinelibrary.wiley.com/doi/full/10.1002/adsc.201901036, which has been published in final form at https://doi.org/10.1002/adsc.201901036. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions.
Text Version
著者版
Gyoseki ID
e37159
OAI-PMH Set
Faculty of Science and Engineering