Chemistry–A European Journal

Controllable Cyclization Reactions of 2??(2′, 3′??Allenyl) acetylacetates Catalyzed by Gold and Palladium Affording Substituted Cyclopentene and 4, 5??Dihydrofuran …

X Jiang, X Ma, Z Zheng, S Ma

Index: Jiang, Xuefeng; Ma, Xiaojing; Zheng, Zilong; Ma, Shengming Chemistry - A European Journal, 2008 , vol. 14, # 28 p. 8572 - 8578

Full Text: HTML

Citation Number: 34

Abstract

Abstract Efficient room-temperature syntheses of cyclopentenes and 4, 5-dihydrofurans with different substitution patterns were performed starting from the same materials (ie, 2-(2′, 3′-allenyl) acetylacetates). Depending on the choice of metal catalyst, the Au-catalyzed reaction afforded C-attack-5-endo cyclization products 2, whereas the Pd-catalyzed one led to the formation of O-attack-5-exo cyclization products 3. The selectivity may be explained ...

Related Articles:

Improved selectivity in the preparation of some 1, 1-difunctionalized 3-cyclopentenes. High yield synthesis of 3-cyclopentenecarboxylic acid

[Depres, Jean-Pierre; Greene, Andrew E. Journal of Organic Chemistry, 1984 , vol. 49, # 5 p. 928 - 931]

More Articles...