1,2:3,4‐Di‐ O ‐isopropylidene‐α‐ d ‐tagatofuranose | Zendy

Watkin David J. | Zendy; Glawar Andreas F. G. | Zendy; Soengas Raquel | Zendy; Skytte Ulla P. | Zendy; Wormald Mark R. | Zendy; Dwek Raymond A. | Zendy; Fleet George W. J. | Zendy

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1,2:3,4‐Di‐ O ‐isopropylidene‐α‐ d ‐tagatofuranose

Author(s) -

Watkin David J.,

Glawar Andreas F. G.,

Soengas Raquel,

Skytte Ulla P.,

Wormald Mark R.,

Dwek Raymond A.,

Fleet George W. J.

Publication year - 2005

Publication title -

acta crystallographica section e

Language(s) - English

Resource type - Journals

ISSN - 1600-5368

DOI - 10.1107/s1600536805025092

Subject(s) - isopropyl , chemistry , anomer , acetal , hydrogen bond , stereochemistry , crystal structure , crystal (programming language) , crystallography , medicinal chemistry , molecule , organic chemistry , computer science , programming language

The crystal structure of diacetone tagatose, C 12 H 20 O 6 , establishes the stereochemistry of the anomeric spiroacetal as 1,2:3,4‐di‐ O ‐isopropylidene‐α‐ d ‐tagatofuranose. Molecules are linked by O—H⋯O hydrogen bonds [O⋯O = 2.862 (2) Å] to form chains running parallel to the b axis.

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