Template‐Assisted meta‐C−H Alkylation and Alkenylation of Arenes. Issue 12 (16th February 2017)

• Record Type: Journal Article
• Authors: Bag, Sukdev; Jayarajan, Ramasamy; Mondal, Rahul; Maiti, Debabrata
• Is Part Of: Angewandte Chemie international edition. Volume 56:Issue 12(2017)
• Page Start: 3182
• Page End: 3186
• Publication Date: 2017-02-16
• Subjects: arenes -- alkenylation -- alkylation -- C−H activation -- palladium; Chemistry -- Periodicals; 540
• DOI: 10.1002/anie.201611360
• Languages: English
• ISSNs: 1433-7851

Abstract

Abstract: To expand the scope of meta ‐functionalization, a pyrimidine‐based template effective for the formation of β‐aryl aldehydes and ketones, using allyl alcohols, by meta ‐C−H activation of benzylsulfonyl esters is described. In addition, α, β‐unsaturated aldehydes were generated by in situ olefination and deprotection of allyl benzyl ethers. These new functionalizations at the meta ‐position of an arene have also been successfully implemented in benzylphosphonate, phenethyl carbonyl, and phenethylsulfonyl ester scaffolds. Key to these successful new functionalizations is the creation of an electropositive palladium center by accepting the electron cloud from the metal to the energetically low‐lying π‐orbitals of pyrimidine ring, and it favors coordination of allyl alcohol to the metal center. Abstract : On target : Pyrimidine‐based, template‐assisted meta ‐C−H alkylation and alkenylation with allyl alcohols and protected allyl alcohols has been developed. Sulfonyl, carbonyl, and phosphonyl esters were used as linkers between the directing group (DG) and target meta ‐C−H bond of arenes.