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On the formation of the 1,2-acetonide of (+), (−), and (±) 1,2,4-butanetriol and its corresponding aldehyde

✍ Scribed by A.I. Meyers; Jon P. Lawson


Book ID
104219748
Publisher
Elsevier Science
Year
1982
Tongue
French
Weight
177 KB
Volume
23
Category
Article
ISSN
0040-4039

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✦ Synopsis


The acetonjdes 1 and 2 are components of a 9 1 equillbrlum establlshed during thelr formatlon

The acetonldes 1 and 2, in enantlomerlc or racemic form, have been utilized by a number


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L-(S)-Erythrulose: The synthesis of (R)-
✍ E. Van der Eycken; H. De Wilde; L. Deprez; M. Vandewalle 📂 Article 📅 1987 🏛 Elsevier Science 🌐 French ⚖ 151 KB

L-(S)-Erythrulose can easily be transformed into (R)-1,2,4-butanetriol and related C4 c\_hiral building blocks. A formal synthesis of (-)GABOB is presented. Also the formation o 3 methylene-1,2,4-butanetriol derivatives is described. Because L-(S)-erythrulose 1 recently became more readily availabl