Palladium‐Catalyzed Chemo‐ and Regioselective Oxidative Cross‐Dehydrogenative Coupling of Acetanilides with Benzothiazole | Zendy

Kianmehr Ebrahim | Zendy; Fardpour Maryam | Zendy; Kharat Ali Nemati | Zendy

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Palladium‐Catalyzed Chemo‐ and Regioselective Oxidative Cross‐Dehydrogenative Coupling of Acetanilides with Benzothiazole

Author(s) -

Kianmehr Ebrahim,

Fardpour Maryam,

Kharat Ali Nemati

Publication year - 2017

Publication title -

european journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.825

H-Index - 155

eISSN - 1099-0690

pISSN - 1434-193X

DOI - 10.1002/ejoc.201700290

Subject(s) - acetanilide , benzothiazole , chemistry , regioselectivity , palladium , catalysis , oxidative phosphorylation , combinatorial chemistry , oxidative coupling of methane , coupling (piping) , organic chemistry , metallurgy , biochemistry , materials science

A practical, versatile, and efficient method for the palladium‐catalyzed direct heteroarylation of acetanilides was developed. In this method, a wide range of acetanilides bearing electron‐donating and electron‐withdrawing groups are well tolerated, and the desired 2‐arylbenzothiazoles are generated in good to high yields through a cross‐dehydrogenative coupling process.

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