Crystal structure of 1,2,3,4-di-O-methylene-α-D-galactopyranose
2015 ◽
Vol 71
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pp. o961-o962
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The title compound, C8H12O6, was synthesized by deacetylation of 6-acetyl-1,2,3,4-di-O-methylene-α-D-galactose with sodium methoxide. The central part of the molecule consists of a six-membered C5O pyranose ring with a twist-boat conformation. Both fused dioxolane rings adopt an envelope conformation with C and O atoms as the flap. In the crystal, O—H...O and C—H...O hydrogen bonds are present between adjacent molecules, generating a three-dimensional network.
2012 ◽
Vol 68
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pp. o2546-o2546
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2016 ◽
Vol 72
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pp. 1219-1222
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2014 ◽
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pp. o1130-o1130
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2015 ◽
Vol 71
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pp. o719-o720
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2014 ◽
Vol 70
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pp. o1029-o1030
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2014 ◽
Vol 70
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pp. o1106-o1106
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2009 ◽
Vol 65
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pp. m683-m683
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2014 ◽
Vol 70
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pp. m53-m53
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2015 ◽
Vol 71
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pp. o492-o493
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2015 ◽
Vol 71
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pp. o477-o478
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