Simple, One‐Pot, and Facile Synthesis of Angularly Fused [6‐7‐5], [6‐7‐6], [6‐7‐7], and [6,7] Ring Systems Using Baylis–Hillman Acetates | Zendy

Basavaiah Deevi | Zendy; Aravindu Kunche | Zendy; Kumar Katta Santosh | Zendy; Reddy Kanumuri Ramesh | Zendy

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Simple, One‐Pot, and Facile Synthesis of Angularly Fused [6‐7‐5], [6‐7‐6], [6‐7‐7], and [6,7] Ring Systems Using Baylis–Hillman Acetates

Author(s) -

Basavaiah Deevi,

Aravindu Kunche,

Kumar Katta Santosh,

Reddy Kanumuri Ramesh

Publication year - 2010

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.200901483

Subject(s) - chemistry , ring (chemistry) , intramolecular force , alkylation , michael reaction , friedel–crafts reaction , simple (philosophy) , organic chemistry , combinatorial chemistry , polymer chemistry , catalysis , philosophy , epistemology

A simple, convenient, and one‐pot synthesis of angularly fused [6‐7‐5], [6‐7‐6], [6‐7‐7], and [6,7] carbocyclic ring systems from Baylis–Hillman acetates through a strategy involving alkylation, formation of a vinyl chloride, and intramolecular cyclization (Friedel–Crafts or Michael reaction) is described.

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