𝔖 Bobbio Scriptorium
✦   LIBER   ✦

On the selectivity of stannylene-mediated alkylation and esterification of methyl 4,6-O-benzylidene α-d-glucopyranoside

✍ Scribed by David J. Jenkins; Barry V.L. Potter

Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
350 KB
Volume
265
Category
Article
ISSN
0008-6215

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Regioselective alkylation, benzoylation,
Regioselective alkylation, benzoylation, and p-toluenesulfonylation of methyl 4,6-O-benzylidene-β-d-glucopyranoside
✍ Ken'ichi Takeo; Kazuko Shibata 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 302 KB

The secondary hydroxyl groups in methyl 4,6-0-benzylidene-/3-Dglucopyranoside (1) show i, towards various reagents, little selectivity in partial etherification and esterification reactions, compared to those in the corresponding cr-D-glucopyranoside derivative. Most of the selective benzylatiorG,

The X-ray crystallographic structures of
The X-ray crystallographic structures of methyl 2-O-methyl-α-d-glucopyranoside and methyl 4,6-O-(S)-benzylidene-2-O-methyl-α-d-galactopyranoside
✍ Patrick McArdle; Desmond Cunningham; Elizabeth Lee; Margaret O'Gara 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 302 KB

As part of a programme involving X-ray crystallographic studies" of cis-and tpuns-fused hexopyranosides, we now report on the crystal structures of methyl 2-~-methyl-~-D-glucop~anoside\* (11, which was obtained by debe~lidenation of methyl 4,~-O-benzyIidene-2-O-methyI-3-O-~-tolylsulfonyl-~-~-glucopy