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The conformational preference of 2-chloromethyl groups in saturated s1x-membered oxygen heterocycles

โœ Scribed by V.M. Gitins(Miss); J.A. Ladd; E. Wyn-Jones; Maxmo Baron


Publisher
Elsevier Science
Year
1973
Tongue
English
Weight
277 KB
Volume
15
Category
Article
ISSN
0022-2860

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X-ray crystallographic analyses are reported for the two title compounds (8 and 9), of which the former crystallized in two modifications (8n and 8b). In all three structures, the pyranose rings have the %, (D) conformation and the substituents at C-l are axial and those at C-24-4 are equatorial. Th