Novel Synthesis of 6‐Substituted 2‐Picolines from Aryl/heteroaryl β‐Enaminones and Meldrum's Acid Using CeCl 3 .7H 2 O/NaI | Zendy

Addla Dinesh | Zendy; Kantevari Srinivas | Zendy

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Novel Synthesis of 6‐Substituted 2‐Picolines from Aryl/heteroaryl β‐Enaminones and Meldrum's Acid Using CeCl 3 .7H 2 O/NaI

Author(s) -

Addla Dinesh,

Kantevari Srinivas

Publication year - 2014

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.1941

Subject(s) - chemistry , meldrum's acid , ammonium acetate , tandem , aryl , regioselectivity , condensation , combinatorial chemistry , ammonium , medicinal chemistry , stereochemistry , organic chemistry , catalysis , materials science , high performance liquid chromatography , alkyl , composite material , physics , thermodynamics

One‐pot condensation of aryl/heteroaryl β‐enaminones, Meldrum's acid, and ammonium acetate in the presence of CeCl 3 .7H 2 O/NaI via tandem Michael addition–cyclodehydration–elimination sequence led to the formation of novel regioselective 6‐substituted 2‐picolines.

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