. alpha.-Nitroarylation of ketones and esters: an exceptionally facile synthesis of indoles, 2-indolinones and arylacetic acids

TV RajanBabu, BL Chenard…

文献索引：RajanBabu, T. V.; Chenard, Bertrand L.; Petti, Michael A. Journal of Organic Chemistry, 1986 , vol. 51, # 10 p. 1704 - 1712

全文：HTML全文

被引用次数: 83

摘要

Silyl enol ethers and ketene silyl acetals add to aromatic nitro compounds in the presence of fluoride ion sources to give dihydroaromatic nitronates which are readily oxidized to a- nitroaryl carbonyl compounds by DDQ or Br,. These versatile intermediates are readily converted into indoles or 2-indolinones by reductive cyclization. Since halogen substituents on the aromatic ring are not displaced in the initial alkylation reaction, nucleophilic ...