Synthesis of (±) 1,2-dideoxy-1,2-diamino-myo-inositol

DOI: 10.1016/0040-4039(94)85318-5

Source and publish data:

Tetrahedron Letters p. 7375 - 7378 (1994)

Update date:2022-08-05

Topics:

Authors:

Guedat, Philippe

Spiess, Bernard

Schlewer, Gilbert

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Article abstract of DOI:10.1016/0040-4039(94)85318-5

Starting from myo-inositol, an isostere, diaminated in positions 1 and 2, was prepared. The key step of the synthesis was the simultaneous inversion of the dimesylate 6 with sodium azide leading to the global retention of the configuration.

Full text of DOI:10.1016/0040-4039(94)85318-5

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Product name:1D-2,3,4,5-tetra-O-benzyl-1,6-O-isopropylidene-myo-inositol

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