Studies on the Tandem Reaction of 4‐Aryl‐2,3‐allenoates with Organozinc Reagents: A Facile Route to Polysubstituted Naphthols | Zendy

Chai Guobi | Zendy; Lu Zhan | Zendy; Fu Chunling | Zendy; Ma Shengming | Zendy

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Studies on the Tandem Reaction of 4‐Aryl‐2,3‐allenoates with Organozinc Reagents: A Facile Route to Polysubstituted Naphthols

Author(s) -

Chai Guobi,

Lu Zhan,

Fu Chunling,

Ma Shengming

Publication year - 2009

Publication title -

chemistry – a european journal

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.687

H-Index - 242

eISSN - 1521-3765

pISSN - 0947-6539

DOI - 10.1002/chem.200901779

Subject(s) - tandem , reagent , aryl , combinatorial chemistry , computer science , scheme (mathematics) , chemistry , database , organic chemistry , engineering , mathematics , mathematical analysis , alkyl , aerospace engineering

Diversified polysubstituted α‐naphthols have been efficiently constructed through a tandem reaction of easily available 2,3‐allenoates and organozinc reagents in moderate to excellent yields (see scheme). Some of the products may undergo a couple of sequential coupling reactions to afford polysubstituted naphthalenes.

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