3,4-O-Isopropyl-idene-2-C-methyl-d-galactonolactone
X-ray crystallography unequivocally confirmed the stereochemistry of the 2-C-methyl group in the title mol-ecule, C(10)H(16)O(6), in which the 1,5-lactone ring exists in a boat conformation. The use of d-galactose in the synthesis determined the absolute stereochemistry. The crystal exists as O-H⋯O...
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Veröffentlicht in: | Acta crystallographica. Section E, Structure reports online Structure reports online, 2010-01, Vol.66 (Pt 2), p.o406-o407 |
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container_title | Acta crystallographica. Section E, Structure reports online |
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creator | Dai, N Jenkinson, S F Fleet, G W J Watkin, D J |
description | X-ray crystallography unequivocally confirmed the stereochemistry of the 2-C-methyl group in the title mol-ecule, C(10)H(16)O(6), in which the 1,5-lactone ring exists in a boat conformation. The use of d-galactose in the synthesis determined the absolute stereochemistry. The crystal exists as O-H⋯O hydrogen-bonded layers in the ab plane, with each mol-ecule acting as a donor and acceptor for two hydrogen bonds. |
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title | 3,4-O-Isopropyl-idene-2-C-methyl-d-galactonolactone |
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