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Structure of 1-amino-1,3-diazaazulene hydrobromide monohydrate

✍ Scribed by Shimanouchi, H. ;Sasada, Y. ;Singh, B.


Book ID
114526504
Publisher
International Union of Crystallography
Year
1979
Weight
282 KB
Volume
35
Category
Article
ISSN
0567-7408

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Recently it has become possible to functionalize the cycloheptatrienone nucleus specifically at either C(2) or C(7).' Briefly, cycloheptatrienones carrying a displaceable group at C(2) react with nucleophiles by competitive paths a and & (Scheme).' Path a is favoured by both mesomerically electron