A Highly Efficient Catalyst for the Suzuki‐Miyaura Cross‐Coupling Reaction of 5‐(5‐chloropyridin‐3‐yl)‐3‐methyl‐1,3,4‐oxadiazol‐2(3 H )‐one | Zendy

Savitha Bhaskaran | Zendy; Koti Reddy Eeda | Zendy; Parthasarathi D. | Zendy; Pakkath Rajeesh | Zendy; Sajith Ayyiliath M. | Zendy; Ananda kumar C. S. | Zendy; Haridas Karickal R. | Zendy; Syed Ali Padusha M. | Zendy

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A Highly Efficient Catalyst for the Suzuki‐Miyaura Cross‐Coupling Reaction of 5‐(5‐chloropyridin‐3‐yl)‐3‐methyl‐1,3,4‐oxadiazol‐2(3 H )‐one

Author(s) -

Savitha Bhaskaran,

Koti Reddy Eeda,

Parthasarathi D.,

Pakkath Rajeesh,

Sajith Ayyiliath M.,

Ananda kumar C. S.,

Haridas Karickal R.,

Syed Ali Padusha M.

Publication year - 2018

Publication title -

journal of heterocyclic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.321

H-Index - 59

eISSN - 1943-5193

pISSN - 0022-152X

DOI - 10.1002/jhet.3280

Subject(s) - chemistry , aryl , catalysis , combinatorial chemistry , boronic acid , suzuki reaction , coupling reaction , coupling (piping) , organic chemistry , medicinal chemistry , palladium , mechanical engineering , alkyl , engineering

A highly efficient protocol for the synthesis of diverse aryl (heteroaryl) substituted pyridyl oxadiazol‐2(3 H )‐one analogues using Suzuki‐Miyaura cross‐coupling strategy under microwave enhanced conditions is developed. The method is found to be compatible with a wide range of aryl (heteroaryl) boronic acids.

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