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A convenient preparation of methyl 4,6-Di-O-acetyl-2,3-dideoxy-β-D-erythro-hex-2-enopyranoside

✍ Scribed by Andrew DeBoer; Christopher J. Thanel; Greg A. Wilson

Publisher
Elsevier Science
Year
1972
Tongue
French
Weight
96 KB
Volume
13
Category
Article
ISSN
0040-4039

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📜 SIMILAR VOLUMES

The preparation and oxyamination of 4,6-
The preparation and oxyamination of 4,6-di-O-acetyl-2,3-dideoxy-α-d-erythro-hex-2-enopyranosyl 4,6-di-O-acetyl-2,3-dideoxy-α-d-erythro-hex-2-enopyranoside. Synthesis of two new diamino derivatives of α-d-mannopyranosyl α-d-mannopyranoside
✍ Hans H. Baer; Lisa Siemsen; Jacques Defaye; Krzysztof Burak 📂 Article 📅 1984 🏛 Elsevier Science 🌐 English ⚖ 967 KB

4,6-Di-O-acetyl-2,3-dideoxy-D-erythro-hex-2-enopyranose (4,6-di-o-acetyl-D-pseudoglucal), prepared from 3,4,6-tri-O-acetyl-1,5-anhydro-2-deoxy-D-arubinohex-1-enitol (tri-0-acetyl-D-glucal), was condensed, by catalysis with boron trifluoride, with an equivalent of the original glycal, to give crystal

Benzotriazol-1-yl 4,6-di-O-acetyl-2,3-di
Benzotriazol-1-yl 4,6-di-O-acetyl-2,3-dideoxy-α-d-erythro-hex-2-enpyranoside
✍ Low, John Nicolson ;Cobo, Justo ;López, M. Dolores ;Nogueras, Manuel ;Sánchez, A 📂 Article 📅 2003 🏛 International Union of Crystallography 🌐 English ⚖ 298 KB

In the title compound {systematic name: [3(S)-acetyloxy-6(S)-(1H-1,2,3-benzotriazol-1-yl)-3,6-dihydro-2H-pyran-2(S)-yl]methyl acetate}, C 16 H 17 N 3 O 5 , weak CÐHÁ Á ÁO hydrogen bonds link the molecules to form a three-dimensional network consisting of linked helical chains.