ISSN:
0009-2940
Schlagwort(e):
Cobaloximes, alkyl-
;
5-Hexenyl, cyclization to cyclopentylmethyl
;
Radicals, alkyl
;
Abstraction of bromine and chlorine
;
Chemistry
;
Inorganic Chemistry
Quelle:
Wiley InterScience Backfile Collection 1832-2000
Thema:
Chemie und Pharmazie
Notizen:
Photochemical cyclization and halogen abstraction reactions of secondary alkylcobaloximes 1b and 1d compared to their primary counterparts 1a and 1c show an enhanced reactivity of secondary alkylcobaloximes: Thus, cyclohexylcobaloxime 1d reacts 13 times faster with CCl4 than n1-hexylcobaloxime 1c, 6-hepten-2-yl-cobaloxime 1b rearranges 58 times faster to its cyclopentylmethyl isomer 4b than 5-hexenylcobaloxime 1a. Although free alkyl radicals are reactive intermediates in photolytic conversions of alkylcobaloximes 1 in organic solvents, the presence of BrCCl3 or bromobenzene in photoreactions of primary alkylcobaloximes 1a and 1c seems to cause a more efficient homolytic cleavage of the Co - C bond.
Zusätzliches Material:
3 Tab.
Materialart:
Digitale Medien
URL:
http://dx.doi.org/10.1002/cber.19931260519
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