4.5 Article

Multi-component Heterocycle Syntheses via Catalytic Generation of Alkynones

Journal

CURRENT ORGANIC CHEMISTRY
Volume 13, Issue 18, Pages 1777-1790

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/138527209789630479

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Funding

  1. Deutsche Forschungsgemeinschaft (DFG)
  2. MORPHOCHEM AG
  3. Fonds der Chemischen Industrie
  4. BASF SE, MERCK Serono
  5. CEM GmbH

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Alkynones are versatile three-carbon building blocks in heterocyclic chemistry. They are easily and efficiently prepared by a modified Sonogashira coupling of acid chlorides and terminal alkynes. As a consequence of the mild reaction conditions the stage is set for new diversity-oriented routes to heterocycles by sequential and consecutive transformations. Hence, isoxazoles, indolizines, pyrazoles, pyridimines, 1,5-benzoheteroazepines, furans, oxazoles, pyrroles, tetrahydro-beta-carbolines, 4H-thiochromen-4-ones and 4H-thiopyrano[2,3-b]pyridin-4-ones are readily accessible by multicomponent coupling-cycloaddition, coupling-addition-cyclocondensation, or coupling-addition-substitution reactions in a one-pot fashion.

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