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Conformations of the antitumor agent 1-(2-chloroethyl)-3-cyclohexyl-1-nitroso-urea in solution studied by 15N-NMR

✍ Scribed by J. William Lown; Shive M.S. Chauhan


Book ID
103397568
Publisher
Elsevier Science
Year
1981
Tongue
French
Weight
201 KB
Volume
22
Category
Article
ISSN
0040-4039

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## Abstract The ^1^H, ^13^C and ^15^N NMR studies have shown that the __E__ and __Z__ isomers of pyrrole‐2‐carbaldehyde oxime adopt preferable conformation with the __syn__ orientation of the oxime group with respect to the pyrrole ring. The __syn__ conformation of __E__ and __Z__ isomers of pyrrol