FeCl3 catalysed regioselective allylation of phenolic substrates with (𝛼-hydroxy)allylphosphonates

Journal of Chemical Sciences

K C Kumara Swamy1¹  Ramesh Kotikalapudi¹  Mandala Anitha¹ 

[1] School of Chemistry, University of Hyderabad, Hyderabad 500 046, Telangana State, India$$

关键词: Allylation;    electrophilic aromatic substitution;    phosphorus;    phenols;    vinylphosphonates;    allylphosphonates.;   

DOI  :  

来源: Indian Academy of Sciences

【 摘 要 】

Electrophilic allylation of phenolic substrates including salicylaldehydes with (𝛼-hydroxy) allylphosphonates is presented. It is observed that catalytic FeCl3 is sufficient to accomplish the allylation. Interestingly, the reaction led to the formation of allylphosphonates in addition to vinylphosphonates, depending upon the substituent. The vinylphosphonates obtained here are 𝐸-isomers. More importantly, the reaction occurred regioselectively with respect to the phenolic substrates. Substituted allylphosphonates are formed when salicylaldehyde or (2-hydroxy-phenyl)arylmethanones are used. Conclusive proof for the formation of allylphosphontates as well as vinylphosphonates has been provided by single crystal X-ray crystallography.

【 授权许可】

Unknown