Efficient Solvent-Free Selective Monoalkylation of Arylacetonitriles with Mono-, Bis-, and Tris-primary Alcohols Catalyzed by a Cp*Ir Complex-Reference-Cited by-同舟云学术

Efficient Solvent-Free Selective Monoalkylation of Arylacetonitriles with Mono-, Bis-, and Tris-primary Alcohols Catalyzed by a Cp*Ir Complex

Published:2006-09-09 Issue:21 Volume:71 Page:8023-8027
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Löfberg Christian¹,Grigg Ronald¹,Whittaker Mark A.¹,Keep Ann¹,Derrick Andrew¹

Affiliation:

1. Molecular, Innovation, Diversity, and Automated Synthesis (MIDAS) Centre, Department of Chemistry, University of Leeds, LS2 9JT, United Kingdom, Johnson Matthey, Orchard Road, Royston, Hertz, SG8 5HE, United Kingdom, and Pfizer, Ramsgate Road, Sandwich, Kent, CT13 9NJ, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo061113p

Reference35 articles.

1. Oxidation of alcohols by transition metal complexes part V. Selective catalytic monoalkylation of arylacetonitriles by alcohols

2. Ruthenium-catalyzed aldol and Michael reactions of activated nitriles

3. Ruthenium-catalyzed aldol and Michael reactions of nitriles. Carbon-carbon bond formation by .alpha.-C-H activation of nitriles.

4. Low-Valent Ruthenium and Iridium Hydride Complexes as Alternatives to Lewis Acid and Base Catalysts

5. Oxidative decyanation of benzyl and benzhydryl cyanides. A simplified procedure

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