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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  and for their importance as key intermediates for the construction of various drugs, biologically active compounds  and naturally occurring alkaloids .