New chiral block for cyclopentanoids synthesis


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Hydroxymethylation of bicyclic allylsilane, (3aR,6R,6aS)-3,3a,6,6a-tetrahydro-6-(trimethylsilyl)-cyclopenta[c]furan-1-one with formaldehyde by Prins reaction proceeds via SE2' mechanism with the formation of anti-addition product. Some reactions of obtained (3aS,4S,6aR)-4-(hydroxymethyl)-3,3a,4,6a-tetrahydro-1H-cyclopenta[c]furan-1-one were investigated.

作者简介

A. Gimazetdinov

Ufa Institute of Chemistry

Email: bioreg@anrb.ru
俄罗斯联邦, pr. Oktyabrya 71, Ufa, 450054

V. Almukhametov

Ufa Institute of Chemistry

Email: bioreg@anrb.ru
俄罗斯联邦, pr. Oktyabrya 71, Ufa, 450054

V. Loza

Ufa Institute of Chemistry

Email: bioreg@anrb.ru
俄罗斯联邦, pr. Oktyabrya 71, Ufa, 450054

M. Miftakhov

Ufa Institute of Chemistry

编辑信件的主要联系方式.
Email: bioreg@anrb.ru
俄罗斯联邦, pr. Oktyabrya 71, Ufa, 450054

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