A direct functionalization of tertiary alkyl bromides with O-, N-, and C-nucleophiles
P Vachal, JM Fletcher, WK Hagmann
Index: Vachal, Petr; Fletcher, Joan M.; Hagmann, William K. Tetrahedron Letters, 2007 , vol. 48, # 33 p. 5761 - 5765
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Citation Number: 5
Abstract
Silver oxide used in stoichiometric amounts promoted the direct functionalization of tert-alkyl bromides and provided the desired adducts in 39–96% isolated yield. Reaction of tert- bromides with carboxylic acids yielded esters, with alcohols and phenols yielded alkyl and aryl ethers, with amines and anilines yielded selectively mono-alkylated amines and anilines, and with a C-nucleophile yielded an all-carbon quaternary hydrocarbon. The ...
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