Tandem Suzuki-Miyaura Coupling/Acid-Catalyzed Cyclization between Vinyl Ether Boronates and Vinyl Halides: A Concise Approach to Polysubstituted Furans | Zendy

Alexey N. Butkevich | Zendy; Lieven Meerpoel | Zendy; Ian Stansfield | Zendy; Patrick Angibaud | Zendy; Andrei Corbu | Zendy; Janine Cossy | Zendy

Open Access

Tandem Suzuki-Miyaura Coupling/Acid-Catalyzed Cyclization between Vinyl Ether Boronates and Vinyl Halides: A Concise Approach to Polysubstituted Furans

Author(s) -

Alexey N. Butkevich,

Lieven Meerpoel,

Ian Stansfield,

Patrick Angibaud,

Andrei Corbu,

Janine Cossy

Publication year - 2013

Publication title -

organic letters

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.94

H-Index - 239

eISSN - 1523-7060

pISSN - 1523-7052

DOI - 10.1021/ol4014574

Subject(s) - chemistry , tandem , dihydropyran , pinacol , catalysis , halide , organic chemistry , boronic acid , coupling (piping) , combinatorial chemistry , mechanical engineering , materials science , engineering , composite material

Polysubstituted 2-(ω-hydroxyalkyl)furans were prepared by tandem Suzuki-Miyaura coupling/acid-catalyzed cyclization starting from appropriately substituted 3-haloallylic alcohols and dihydrofuran-, dihydropyran- or glycal-derived pinacol boronates.

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