Studies towards a biomimetic synthesis of α-cyclopiazonic acid: Synthesis of 5-substituted isoxazole-4-carboxylic esters

Autor:	Rachel A. Stenson, Eoghan M. McGarrigle, Vijayalakshmi A. Moorthie, Varinder K. Aggarwal
Předmět:	Tosylhydrazone Sulfonium Organic Chemistry Acetoacetic ester synthesis Chloroacetyl chloride lcsh:QD241-441 chemistry.chemical_compound chemistry lcsh:Organic chemistry Biomimetic synthesis Ethyl acetoacetate Organic chemistry Isoxazole Tetrahydrothiophene
Zdroj:	University of Bristol-PURE ARKIVOC, Vol 2007, Iss 5, Pp 139-151 (2006)
Popis:	An efficient, high yielding synthesis of ethyl 5-hydroxymethyl-3-methylisoxazole-4-carboxylate has been developed, based on a procedure by Gelin which involves reaction of ethyl acetoacetate with chloroacetyl chloride followed by treatment with hydroxylamine hydrochloride. The product of this reaction was then converted into the bromide and reacted with tetrahydrothiophene to give sulfonium salts in up to 71% overall yield (from ethyl acetoacetate). The synthesis is suitable for use with a chiral sulfide and for large-scale use. The synthesis of ethyl 5-formyl-3-methyl-4-isoxazolecarboxylate and the corresponding tosylhydrazone are also reported. These isoxazoles are starting materials for a proposed convergent, biomimetic synthesis of α-cyclopiazonic acid.
Databáze:	OpenAIRE
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