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A Versatile Method for the Elaboration of Diversely Substituted N-Alkylated and Free-NH Isoindolinones. Application to the Asymmetric Synthesis of the C3-Substituted Models
Published:
30 November 2007
by MDPI
in The 11th International Electronic Conference on Synthetic Organic Chemistry
session General Organic Synthesis
Abstract: Isoindolinones and their derivatives of generic structure 1, 2 have gained considerable attention due to their diverse physiological and chemotherapeutic activities [1] and for their importance as key intermediates for the construction of various drugs, biologically active compounds [2] and naturally occurring alkaloids [3].
Keywords: n/a
