How Can Fluctional Chiral Lanthanide (III) Complexes Achieve a High Stereoselectivity in Aqueous Mukaiyama-Aldol Reaction?-Reference-Cited by-同舟云学术

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How Can Fluctional Chiral Lanthanide (III) Complexes Achieve a High Stereoselectivity in Aqueous Mukaiyama-Aldol Reaction?

Published:2015-05-21 Issue:6 Volume:5 Page:3731-3739
ISSN:2155-5435
Container-title:ACS Catalysis
language:en
Short-container-title:ACS Catal.

Author:

Hatanaka Miho¹,Morokuma Keiji¹

Affiliation:

1. Fukui Institute for Fundamental Chemistry, Kyoto University, Kyoto 606-8103, Japan

Funder

Ministry of Education, Culture, Sports, Science, and Technology

Kyoto University

Publisher

American Chemical Society (ACS)

Subject

Catalysis,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acscatal.5b00438

Reference60 articles.

1. Green chemistry, green solvents, and free radical reactions in aqueous media

2. Acceleration of Organic Reactions through Aqueous Solvent Effects

3. Hydrophilic Ligands and Their Application in Aqueous-Phase Metal-Catalyzed Reactions

4. Water: Nature’s Reaction Enforcer—Comparative Effects for Organic Synthesis “In-Water” and “On-Water”

5. Green chemistry oriented organic synthesis in water

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2. Revealing the Strong Relationships between Ligand Conformers and Activation Barriers: A Case Study of Bisphosphine Reductive Elimination;ACS Catalysis;2020-06-03

3. Artificial Force-Induced Reaction Method for Systematic Elucidation of Mechanism and Selectivity in Organometallic Reactions;New Directions in the Modeling of Organometallic Reactions;2020

4. Trialkylsulfonium and Tetraalkylammonium Salts as Hydrogen-Bonding Catalysts in an Aza-Diels-Alder Reaction: Experimental and Computational Studies;HETEROCYCLES;2020

5. The Origins of the Stereoselectivity and Enantioswitch in the Rare‐Earth‐Catalyzed Michael Addition: A Computational Study;ChemCatChem;2019-06-13

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