Passerini and Ugi reactions of anomeric glucosyl isonitriles
✍ Scribed by Thomas Ziegler; Rolf Schlömer; Christoph Koch
- Book ID
- 104259642
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 198 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Acetyl and benzyl protected 13-D-glucopyranosyl isonitriles were treated with various aldehydes and acetic acid to give the corresponding Passerini reaction products and with i-butanal, carboxylic acids and amines to give the corresponding Ugi reaction products, respectively. No significant diastereoselectivity was observed for both reactions.
📜 SIMILAR VOLUMES
Acetyl and benzyl protected anomeric [~-D-glucopyrunosyl isonitriles and 1,3,4,6-tetra-Oacetyl-2-dcoxy-2-isocyano-13-D-glucopyranose were treated with various carbonyl compounds and, carboxylic acids to give the corresponding Passerini reaction products and with i-butanal, carboxylic acids and amine