Journal article
2,5-Anhydro-N-benzyl-2-C-methyl-D-arabinonamide [(2S,3R,4R)-N-benzyl-3,4-dihydroxy-2-methyltetrahydrofuran-2-carboxamide]
- Abstract:
- The size of the ring and relative configuration of the chiral centres in the title compound, C13H17NO4, formed by the preferential formation of the hindered five-membered ring tetrahydrofuran rather than the expected three-membered ring epoxide, was established by X-ray crystallographic analysis; the absolute configuration was determined by the use of 2-C-methyl-D-arabinono-lactone as the starting material. The crystal structure consists of hydrogen-bonded layers lying with their hydrophobic surfaces in contact. © 2007 International Union of Crystallography All rights reserved.
- Publication status:
- Published
Actions
Authors
- Journal:
- ACTA CRYSTALLOGRAPHICA SECTION E-STRUCTURE REPORTS ONLINE More from this journal
- Volume:
- 63
- Issue:
- 2
- Pages:
- O574-O576
- Publication date:
- 2007-02-01
- DOI:
- EISSN:
-
1600-5368
- ISSN:
-
1600-5368
- Language:
-
English
- Pubs id:
-
pubs:40268
- UUID:
-
uuid:cfdfb83e-61c1-47a0-88c1-b7802b1728ca
- Local pid:
-
pubs:40268
- Source identifiers:
-
40268
- Deposit date:
-
2012-12-19
Terms of use
- Copyright date:
- 2007
If you are the owner of this record, you can report an update to it here: Report update to this record