Copper‐Catalyzed Four‐Component Reaction of Baylis–Hillman Adducts with Alkynes, Sulfonyl Azides and Alcohols | Zendy

Song Wangze | Zendy; Lei Ming | Zendy; Shen Yang | Zendy; Cai Shuying | Zendy; Lu Wei | Zendy; Lu Ping | Zendy; Wang Yanguang | Zendy

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Copper‐Catalyzed Four‐Component Reaction of Baylis–Hillman Adducts with Alkynes, Sulfonyl Azides and Alcohols

Author(s) -

Song Wangze,

Lei Ming,

Shen Yang,

Cai Shuying,

Lu Wei,

Lu Ping,

Wang Yanguang

Publication year - 2010

Publication title -

advanced synthesis and catalysis

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 1.541

H-Index - 155

eISSN - 1615-4169

pISSN - 1615-4150

DOI - 10.1002/adsc.201000400

Subject(s) - chemistry , sulfonyl , adduct , catalysis , methylene , copper , component (thermodynamics) , organic chemistry , medicinal chemistry , alkyl , physics , thermodynamics

4‐(Alkoxycarbonyl)‐pent‐4‐enimidates were regioselectively synthesized via a copper‐catalyzed four‐component reaction of Baylis–Hillman adducts with terminal alkynes, sulfonyl azides and alcohols. The procedure is concise, general and efficient. The resulting pentenimidates could be further transformed to 3‐methylene‐2,3‐dihydroindene‐1‐imidates.

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