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1,6:3,4-Dian­hydro-2-azido-2-deoxy-β-d-galactopyran­ose

✍ Scribed by Barnes, John C. ;Brimacombe, John S. ;Paterson, Michael J.


Publisher
International Union of Crystallography
Year
2002
Tongue
English
Weight
188 KB
Volume
58
Category
Article
ISSN
1600-5368

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✦ Synopsis


In the title compound, C 6 H 7 N 3 O 3 , the presence of the epoxide group modi®es the bonding in the sugar ring so that the ®ve C atoms within it are coplanar, with a shortening of the formally single CÐC bonds to an average of 1.475 (8) A Ê .


📜 SIMILAR VOLUMES


Crystal and molecular structure of 1,6:3
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The opening ot" oxirane rings o1' dianhydro sugars with high regiosclectivily can afford many chiral intermediates Ibr controlling asymmetric syntheses [I-5]. Here, wc report the crystal structure o1' 1,6:3,4~diallhydro-2-Ool~-lolylsullbnyl-~-D°galactopyranose (!) which may provide helpl'ul i111' o1

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The molecular structure of the title compound, C 6 H 9 IO 4 , is similar to that of 1,6-anhydro--d-glucopyranose. The crystal packing shows strong intermolecular O-HÁ Á ÁO and C-HÁ Á ÁI hydrogen bonds.

3-Azido-3-deoxy-2,2′:5,6-di-O-iso­propyl
✍ Harding, Christopher C. ;Shallard-Brown, Howard ;Watkin, David J. ;Soengas, Raqu 📂 Article 📅 2004 🏛 International Union of Crystallography 🌐 English ⚖ 897 KB

Single-crystal X-ray study T = 120 K Mean '(C±C) = 0.005 A Ê R factor = 0.045 wR factor = 0.108 Data-to-parameter ratio = 9.3 For details of how these key indicators were automatically derived from the article, see http://journals.iucr.org/e.