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The Journal of organic chemistry

Reaction of nitro anions with N, N-dimethyl-p-hydroxybenzylamine. New synthesis of. alpha.-methyltyrosine

WS Saari

文献索引:Saari,W.S. Journal of Organic Chemistry, 1967 , vol. 32, p. 4074 - 4076

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被引用次数: 6

摘要

Isolation of predominately C-alkylation products in these reactions may be due in part to a dissociation of the less stable 0-alkylation product, the nitronic ester 7, to the original nitro anion and 6 and eventual realkylation at carbon to give the more stable C-alkylated product. loaSb