Artigo Revisado por pares

Stereoselective synthesis of anti-1,3-diol units via Prins cyclisation: application to the synthesis of (−)-sedamine

2006; Elsevier BV; Volume: 47; Issue: 26 Linguagem: Inglês

10.1016/j.tetlet.2006.04.102

ISSN

1873-3581

Autores

J. S. Yadav, Maddi Sridhar Reddy, P. Purushothama Rao, A. R. Prasad,

Tópico(s)

Marine Sponges and Natural Products

Resumo

The scope of the Prins cyclisation, the higher stereoselective synthesis of multisubstituted tetrahydropyrans from aldehydes and homoallylic alcohols, is expanded. A new approach for the stereoselective synthesis of polyketide precursors containing anti-1,3-diols, flanked by a variety of alkyl branches and functional groups is described. The approach is successfully exploited for the synthesis of (−)-sedamine.

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