Novel TSAO Derivatives Modified at Positions 3′ and 4′ Of the Spiro Moiety
Article 1999 en
Authors
EL
Esther Lobatón
SV
Sonsoles Velázquez
AS
Ana San‐Félix
Abstract
1 min read
We have explored the introduction of different functional groups at positions 3" and 4" of the spiro moiety of TSAO-T. Alkylation of this spiro moiety afforded mixtures of N and/or C-alkylated derivatives, while acylation occurs, exclusively, on the amino group. Position 3" has been selectively functionalized by halogenation followed by Stille-cross coupling reaction with organostannanes under a variety of experimental conditions.
Sonia de Castro, Esther Lobatón, María‐Jesús Pérez‐Pérez, Ana San‐Félix, Alessandra Cordeiro, Graciela Andreï, Robert Snoeck, De Clercq Erik, Jan Balzarini, Marı́a-José Camarasa, Sonsoles Velázquez
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