Diastereoselective Reductive Etherification Via High-Throughput Experimentation: Access to Pharmaceutically Relevant Alkyl Ethers-Reference-Cited by-同舟云学术

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Diastereoselective Reductive Etherification Via High-Throughput Experimentation: Access to Pharmaceutically Relevant Alkyl Ethers

Published:2023-09-07 Issue:19 Volume:88 Page:13454-13465
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Fu Jiantao¹^ORCID,Vaughn Zoe¹,Nolting Andrew F.²^ORCID,Gao Qi³^ORCID,Yang Dexi¹,Schuster Christopher H.²,Kalyani Dipannita¹^ORCID

Affiliation:

1. Discovery Chemistry, Merck & Co., Inc., Kenilworth, New Jersey 07033, United States

2. Process Research and Development, Merck & Co., Inc., Rahway, New Jersey 07065, United States

3. Analytical Research and Development, Merck & Co., Inc., Kenilworth, New Jersey 07033, United States

Funder

Merck

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c00822

Reference45 articles.

1. C–O Bond Formation through Transition Metal-mediated Etherification

2. XLV. Theory of ætherification

3. Selective Catalytic Synthesis of Unsymmetrical Ethers from the Dehydrative Etherification of Two Different Alcohols

4. Production of Biomass-Based Automotive Lubricants by Reductive Etherification

5. Chemoselective Formation of Unsymmetrically Substituted Ethers from Catalytic Reductive Coupling of Aldehydes and Ketones with Alcohols in Aqueous Solution

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1. Zinc-Catalyzed Cyclization of Alkynyl Derivatives: Substrate Scope and Mechanistic Insights;Inorganic Chemistry;2024-07-16

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