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Unexpected formation of a d-chiro inositol from a l-chiro precursor

✍ Scribed by Ralf Miethchen; Christian Sowa; Manfred Michalik

Publisher
Elsevier Science
Year
2001
Tongue
French
Weight
153 KB
Volume
42
Category
Article
ISSN
0040-4039

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πŸ“œ SIMILAR VOLUMES

Enantiospecific synthesis of a different
Enantiospecific synthesis of a differentially protected L-chiro-inositol from D-xylose
✍ Alexander Kornienko; Marc d'Alarcao πŸ“‚ Article πŸ“… 1997 πŸ› Elsevier Science 🌐 French βš– 201 KB

A convenient synthesis of diffenmfially protected L-ch/ro-inositol 7 from 2,3,4-tri-Obenzyl-D-xylopyranose is describod. The stmcUa~ of 7 was confnmcd by its W~asformation to the pentabenzylated derivative of(-)-quetrachitoi.

Stereoselective Synthesis of myo-, neo-,
Stereoselective Synthesis of myo-, neo-, L-chiro, D-chiro, allo-, scyllo-, and epi-Inositol Systems via Conduritols Prepared from p-Benzoquinone
✍ Michael Podeschwa; Oliver Plettenburg; Jochen vomΒ Brocke; Oliver Block; Stephan πŸ“‚ Article πŸ“… 2003 πŸ› John Wiley and Sons 🌐 English βš– 280 KB

## Abstract A practical route is described for the flexible preparation of a wide variety of inositol stereoisomers and their polyphosphates. The potential of this approach is demonstrated by the synthesis of __myo__‐, L‐__chiro__‐, D‐__chiro__‐, __epi__‐, __scyllo__‐, __allo__‐, and __neo__‐inosit