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X-ray and proton NMR analyses of the structure and conformation of 2-azacoformycin, a potent inhibitor of adenosine deaminase

✍ Scribed by Birnbaum, George I.; Brisson, Jean Robert; Krawczyk, Steven H.; Townsend, Leroy B.


Book ID
126883997
Publisher
American Chemical Society
Year
1985
Tongue
English
Weight
731 KB
Volume
107
Category
Article
ISSN
0002-7863

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A Conformational Study of [3.3](2,6)Pyri
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## Abstract A variable‐temperature ^1^H‐NMR study and X‐ray structural analysis show that the most stable conformational isomer of [3.3](2,6)pyridinophane 2 is the __syn__(boat‐boat) conformer, and the relative stability order of the three stable conformers is __syn__(boat‐boat) > __syn__(chair‐boa