DIVERISITY ORIENTED APPROACH TO SPIROBARBITURIC ACID DERIVATIVES VIA A [2+2+2] CYCLOADDITION AND DIELS-ALDER REACTION AS KEY STEPS

KOTHA, S
ALI, R

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Publication date

January 2014

DOI

10.3987/COM-13-S(S)48

Publisher

Japan Institute of Heterocyclic Chemistry

Journal

Heterocycles

Abstract

Spirobarbituric acid derivatives are assembled via a [2+2+2] cycloaddition and the Diels-Alder (DA) reaction as key steps. A transient diene 13 containing spiribarbituric acid suitable for DA reaction has been generated in situ from the sultine derivative 12, which in turn was obtained by the usage of rongalite

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DIVERISITY ORIENTED APPROACH TO SPIROBARBITURIC ACID DERIVATIVES VIA A [2+2+2] CYCLOADDITION AND DIELS-ALDER REACTION AS KEY STEPS

Abstract

Extracted data

DIVERISITY ORIENTED APPROACH TO SPIROBARBITURIC ACID DERIVATIVES VIA A [2+2+2] CYCLOADDITION AND DIELS-ALDER REACTION AS KEY STEPS

Abstract

Extracted data

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