» Articles » PMID: 34237201

Catalytic Reductive Alcohol Etherifications with Carbonyl-Based Compounds or CO and Related Transformations for the Synthesis of Ether Derivatives

Overview
Journal ChemSusChem
Specialty Chemistry
Date 2021 Jul 8
PMID 34237201
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Ether derivatives have myriad applications in several areas of chemical industry and academia. Hence, the development of more effective and sustainable protocols for their production is highly desired. Among the different methodologies reported for ether synthesis, catalytic reductive alcohol etherifications with carbonyl-based moieties (aldehydes/ketones and carboxylic acid derivatives) have emerged in the last years as a potential tool. These processes constitute appealing routes for the selective production of both symmetrical and asymmetrical ethers (including O-heterocycles) with an increased molecular complexity. Likewise, ester-to-ether catalytic reductions and hydrogenative alcohol etherifications with CO to dialkoxymethanes and other acetals, albeit in less extent, have undergone important advances, too. In this Review, an update of the recent progresses in the area of catalytic reductive alcohol etherifications using carbonyl-based compounds and CO have been described with a special focus on organic synthetic applications and catalyst design. Complementarily, recent progress made in catalytic acetal/ketal-to-ether or ester-to-ether reductions and other related transformations have been also summarized.

Citing Articles

Direct carbonyl reductive functionalizations by diphenylphosphine oxide.

Liu F, Dong J, Cheng R, Yin S, Chen L, Su L Sci Adv. 2025; 11(6):eads4626.

PMID: 39919176 PMC: 11804924. DOI: 10.1126/sciadv.ads4626.


Selective reductive conversion of CO to CH-bridged compounds by using a Fe-functionalized graphene oxide-based catalyst.

Ghosh S, Ariya P Commun Mater. 2024; 5(1):196.

PMID: 39430061 PMC: 11488465. DOI: 10.1038/s43246-024-00639-5.


Enable biomass-derived alcohols mediated alkylation and transfer hydrogenation.

Liu X, Huang L, Ma Y, She G, Zhou P, Zhu L Nat Commun. 2024; 15(1):7012.

PMID: 39147765 PMC: 11327299. DOI: 10.1038/s41467-024-51307-8.


Novel chalcone-based crown ethers: synthesis, characterization, antioxidant activity, biological evaluations, and wastewater remediation.

Ahmad M, Hawaiz F RSC Adv. 2024; 14(4):2369-2379.

PMID: 38213971 PMC: 10783163. DOI: 10.1039/d3ra08133h.


Hydrophobic Drug Carrier from Polycaprolactone--Poly(Ethylene Glycol) Star-Shaped Polymers Hydrogel Blend as Potential for Wound Healing Application.

Ahmad Shariff S, Daik R, Haris M, Ismail M Polymers (Basel). 2023; 15(9).

PMID: 37177238 PMC: 10181117. DOI: 10.3390/polym15092072.


References
1.
Chen C, Wang C, Li X, Witek H, Mong K . Sub-stoichiometric reductive etherification of carbohydrate substrates and one-pot protecting group manipulation. Org Biomol Chem. 2020; 18(16):3135-3141. DOI: 10.1039/d0ob00252f. View

2.
Rorrer J, Pindi S, Toste F, Bell A . Effect of Alcohol Structure on the Kinetics of Etherification and Dehydration over Tungstated Zirconia. ChemSusChem. 2018; 11(18):3104-3111. DOI: 10.1002/cssc.201801067. View

3.
Wang W, Wang S, Ma X, Gong J . Recent advances in catalytic hydrogenation of carbon dioxide. Chem Soc Rev. 2011; 40(7):3703-27. DOI: 10.1039/c1cs15008a. View

4.
Lange J, van der Heide E, van Buijtenen J, Price R . Furfural--a promising platform for lignocellulosic biofuels. ChemSusChem. 2012; 5(1):150-66. DOI: 10.1002/cssc.201100648. View

5.
Thenert K, Beydoun K, Wiesenthal J, Leitner W, Klankermayer J . Ruthenium-Catalyzed Synthesis of Dialkoxymethane Ethers Utilizing Carbon Dioxide and Molecular Hydrogen. Angew Chem Int Ed Engl. 2016; 55(40):12266-9. DOI: 10.1002/anie.201606427. View