A versatile synthetic route to indolizidines, (+)-7-deoxy-6- epicastanospermine, (-)-7,8-dideoxy-6-epicastanospermine and (-)-N- acetylslaframine

DOI: 10.1016/S0040-4039(98)02051-6

Source and publish data:

Tetrahedron Letters p. 9047 - 9050 (1998)

Update date:2022-08-03

Topics:

Authors:

Kang, Sung Ho

Kim, Joon Seop

Youn, Joo-Hack

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Article abstract of DOI:10.1016/S0040-4039(98)02051-6

(+)-7-Deoxy-6-epicastanospermine 1, (-)-7,8-dideoxy-6- epicastanospermine 2 and (-)-N-acetylslaframine 4 have been synthesized via the stereoselective intramolecular iodocyclization of trichloroacetimidates generated from cis-olefinic allylic alcohols 7 a

Full text of DOI:10.1016/S0040-4039(98)02051-6

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Product name:((1S,6S,8aS)-1-Hydroxy-octahydro-indolizin-6-yl)-carbamic acid tert-butyl ester

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