Enhanced Activity and Enantioselectivity of Henry Reaction by the Postsynthetic Reduction Modification for a Chiral Cu(salen)-Based Metal–Organic Framework-Reference-Cited by-同舟云学术

Enhanced Activity and Enantioselectivity of Henry Reaction by the Postsynthetic Reduction Modification for a Chiral Cu(salen)-Based Metal–Organic Framework

Published:2018-09-10 Issue:19 Volume:57 Page:11986-11994
ISSN:0020-1669
Container-title:Inorganic Chemistry
language:en
Short-container-title:Inorg. Chem.

Author:

Fan Yamei¹,Ren Yanwei¹^ORCID,Li Jiawei¹,Yue Chenglong¹,Jiang Huanfeng¹^ORCID

Affiliation:

1. Key Laboratory of Functional Molecular Engineering of Guangdong Province, School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, 510641, P. R. China

Funder

Ministry of Science and Technology of the People's Republic of China

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.inorgchem.8b01551

Reference67 articles.

1. [Ln(binolam)3]⋅(OTf)3, a New Class of Propeller-Shaped Lanthanide(III) Salt Complexes as Enantioselective Catalysts: Structure, Dynamics and Mechanistic Insight

2. Probing the evolution of an Ar-BINMOL-derived salen–Co(iii) complex for asymmetric Henry reactions of aromatic aldehydes: salan–Cu(ii) versus salen–Co(iii) catalysis