Cycloaddition Reactions of Carbohydrate Derivatives. Part III. A New Route to Swainsonine Analogs.

DOI: 10.1016/S0040-4039(00)79832-7

Source and publish data:

Tetrahedron Letters p. 3133 - 3136 (1992)

Update date:2022-07-30

Topics:

Authors:

Herczegh, Pal

Kovacs, Imre

Szilagyi, Laszlo

Zsely, Martina

Sztaricskai, Ferenc

et al. et al.

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Article abstract of DOI:10.1016/S0040-4039(00)79832-7

Swainsonine analogs 10 and 12 have been synthesized from D- and L-arabinose, respectively, using cyclocondensation of azomethines with Danisthefsky's diene followed by stereoselective carbonyl and double bond reduction of the resulting pyridones, chain sh

Full text of DOI:10.1016/S0040-4039(00)79832-7

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