One-pot synthesis of 1-allyl- and 1-allenyl-6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glycosides from methyl tetra-O-benzyl-α-D-glycosides
✍ Scribed by Shang-Cheng Hung; Chun-Cheng Lin; Chi-Huey Wong
- Book ID
- 104257559
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 180 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
A one-pot synthesis of 1-allyl-and 1-allenyl-6-O-acetyl-2,3,4-tri-O-benzyl-ot-D-glycosides from the corresponding methyl per-benzyl-tx-D-glycosides and allyl trimethylsilane or propargyl trimethylsilane in the presence of trimethylsilyl trifluoromethanesulfonate followed by addition of acetic anhydride in good yields was described
📜 SIMILAR VOLUMES
Benzyl 2-acetamido-2-deoxy-3-O-methyl-alpha-D-glucopyranoside (3) was obtained by deacetalation of its 4,6-O-benzylidene derivative (2). Compound 2 was prepared by methylation of benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-alpha-D-glucopyranoside with methyl iodide-silver oxide in N,N-dimethylforma
Acylated ]3-o-xylopyranose derivatives are known to exist as a mixture of the 1C 4 and 4C I conformers in rapid equilibrium in solution [3]. Several conformations have also been reported for/3-D-xylopyranose derivatives in the solid state [4]. In the course of our study to investigate the functions