Selective synthesis of Neu5Ac2en and its oxazoline derivative using BF3·Et2O
✍ Scribed by Goreti Ribeiro Morais; Rudi Santiago Oliveira; Robert A. Falconer
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- French
- Weight
- 298 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Application of the Lewis acid BF 3 ÁEt 2 O to the selective synthesis of 5-acetamido-2,6-anhydro-3,5-dideoxy-D-glycero-D-galacto-non-2-enonic acid (Neu5Ac2en) and the related oxazoline, methyl 7,8,9-tri-Oacetyl-2,3,4,5-tetradeoxy-2,3-didehydro-2,3-trideoxy-4 0 ,5 0 -dihydro-2 0 -methyloxazolo[5,4-d]-D-glycero-D-talo-non-2-enonate is described.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Alkyl iodides are prepared in high yields by treatment of allylic and benzylic alcohols with an equimolar amount of KI in the presence of BF 3 •Et 2 O in dioxane under mild conditions.