Cycloalkenyl nonaflates as electrophilic cross-coupling substrates for palladium catalyzed C–N bond forming reactions with enolizable heterocycles under microwave enhanced conditions-Reference-Cited by-同舟云学术

Cycloalkenyl nonaflates as electrophilic cross-coupling substrates for palladium catalyzed C–N bond forming reactions with enolizable heterocycles under microwave enhanced conditions

Published:2014 Issue:3 Volume:38 Page:1294
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Abdul Khader K. K.,Sajith Ayyiliath. M.,Syed Ali Padusha M.,Nagaswarupa H. P.,Muralidharan A.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2014/NJ/C3NJ01355C

Reference53 articles.

1. Palladium-Catalyzed Amination of Aryl Nonaflates

2. Diazonium Salts as Substrates in Palladium-Catalyzed Cross-Coupling Reactions

3. Applications of and alternatives to π-electron-deficient azine organometallics in metal catalyzed cross-coupling reactions

4. Palladium-Catalyzed Amination of Aryl and Heteroaryl Tosylates at Room Temperature

5. Zinc Trimethylsilylamide as a Mild Ammonia Equivalent and Base for the Amination of Aryl Halides and Triflates

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