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Concise route to defined stereoisomers of the hydroxy acid of the chondramides.

ABSTRACT: The use of Kobayashi vinylogous aldol reaction in the reaction with acetaldehyde led to anti-aldol product 11. After reductive removal of the chiral auxiliary, the primary alcohol was converted to the allyliodide 14. This compound could be engaged in an Evans alkylation reaction, leading eventually to hydroxy acid 19. Inclusion of a Mitsunobu inversion reaction on the sequence starting with ent-11 led to hydroxy ester 30, featuring a 6,7-syn-configuration. These hydroxy acids should help to elucidate the correct stereostructure of the chondramide depsipeptides.

SUBMITTER: Schmauder A

PROVIDER: S-EPMC3228260 | biostudies-literature | 2008 Jun

REPOSITORIES: biostudies-literature

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Concise route to defined stereoisomers of the hydroxy acid of the chondramides.

Schmauder Anke A Müller Sven S Maier Martin E ME

Tetrahedron 20080601 27

The use of Kobayashi vinylogous aldol reaction in the reaction with acetaldehyde led to anti-aldol product 11. After reductive removal of the chiral auxiliary, the primary alcohol was converted to the allyliodide 14. This compound could be engaged in an Evans alkylation reaction, leading eventually to hydroxy acid 19. Inclusion of a Mitsunobu inversion reaction on the sequence starting with ent-11 led to hydroxy ester 30, featuring a 6,7-syn-configuration. These hydroxy acids should help to eluc ...[more]

PMID: 22140278

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