The Acrylamide Moiety as an Activated Alkene Component in the Intramolecular Baylis–Hillman Reaction: Facile Synthesis of Functionalized α‐Methylene Lactam and Spirolactam Frameworks | Zendy

Basavaiah Deevi | Zendy; Reddy Guddeti Chandrashekar | Zendy; Bharadwaj Kishor Chandra | Zendy

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The Acrylamide Moiety as an Activated Alkene Component in the Intramolecular Baylis–Hillman Reaction: Facile Synthesis of Functionalized α‐Methylene Lactam and Spirolactam Frameworks

Author(s) -

Basavaiah Deevi,

Reddy Guddeti Chandrashekar,

Bharadwaj Kishor Chandra

Publication year - 2014

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.201301526

Subject(s) - moiety , chemistry , alkene , methylene , intramolecular force , baylis–hillman reaction , combinatorial chemistry , acrylamide , organic chemistry , adduct , catalysis , polymer , copolymer

A facile strategy for the intramolecular Baylis–Hillman reaction by utilizing an acrylamide moiety as an activated alkene component was developed, which thus provides a convenient protocol for obtaining five‐ and six‐membered α‐methylene lactam and spirolactam derivatives.

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