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Chemistry of carbonnitrogen multiple bonds. The useful synthon CF2NBr

✍ Scribed by D.D. DesMarteau; B.A. O'Brien; C.W. Bauknight Jr.; S. Singh; S. Hwang; W. Storzer


Book ID
104150057
Publisher
Elsevier Science
Year
1985
Tongue
English
Weight
26 KB
Volume
29
Category
Article
ISSN
0022-1139

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✦ Synopsis


Improvements in the synthesis of g-bromo-difluoromethanimine, CF2=NBr. will be described along with some reaction chemistry. The imine undergoes thermal addition with a variety of olefins, leading to the simple addition product and to the formation of telomers. Photolysis with CO forms the isocyanate BrCF2tJ=C=0, in high yield. Pyrolysis of CF2=UBr at -450°C gives high yields of tetrafluoro-2,3-diara-1,3butadiene, CF24WJ=CF2. making this compound readily available for the first time. Some new reaction chemistry of the diene will be discussed.


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