Direct Access to Isotopically Labeled Aliphatic Ketones Mediated by Nickel(I) Activation-Reference-Cited by-同舟云学术

Direct Access to Isotopically Labeled Aliphatic Ketones Mediated by Nickel(I) Activation

Published:2020-03-02 Issue:21 Volume:59 Page:8099-8103
ISSN:1433-7851
Container-title:Angewandte Chemie International Edition
language:en
Short-container-title:Angew. Chem. Int. Ed.

Author:

Donslund Aske S.¹,Pedersen Simon S.¹,Gaardbo Cecilie¹,Neumann Karoline T.¹,Kingston Lee²,Elmore Charles S.²,Skrydstrup Troels¹^ORCID

Affiliation:

1. Carbon Dioxide Activation Center (CADIAC)Department of Chemistry and the Interdisciplinary Nanoscience Center (iNANO)Aarhus University Gustav Wieds Vej 14 8000 Aarhus C Denmark

2. Isotope ChemistryEarly Chemical DevelopmentPharmaceutical Sciences, R&DAstraZeneca Pharmaceuticals 43183 Gothenberg Sweden

Funder

Danmarks Grundforskningsfond

NordForsk

Naturvidenskab og Teknologi, Aarhus Universitet

Lundbeckfonden

Publisher

Wiley

Subject

General Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/anie.201916391

Reference61 articles.

1. Reaction of acyl chlorides with organometallic reagents: A banquet table of metals for ketone synthesis

2. For selected examples see:

3. Reduction of Aldehydes, Ketones and Acid Chlorides by Sodium Borohydride

4. Large-Scale Carbonyl Reductions in the Pharmaceutical Industry

5. Reductive Amination of Aldehydes and Ketones with Sodium Triacetoxyborohydride. Studies on Direct and Indirect Reductive Amination Procedures1

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