Preparation of 4,5-Dihydronaphth[2,1-c]isoxazoles from Dilithiated 2-Tetralone Oxime and Select Esters.

Autor: Choi, Emily, Knight, JohnD., Malatanos, MariaD., Rhett, J.Matthew, Walters, MatthewJ., Dunn, S.Patrick, Beam, CharlesF.
Předmět:
Zdroj: Synthetic Communications; 2008, Vol. 38 Issue 5, p713-722, 10p, 2 Diagrams
Abstrakt: Dilithiated 2-tetralone oxime, prepared in excess lithium diisopropylamide, was condensed with aromatic esters, such as methyl 4-methoxybenzoate, followed by cyclization of the C-acylated intermediate with aqueous acid to give dihydronaphthisoxazoles, 4,5-dihydronaphth[2,1-c]isoxazoles. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index
Nepřihlášeným uživatelům se plný text nezobrazuje