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Photochemistry of threeN-acetoacetyl amino acid methyl esters: structure elucidation of the radiation products by gas chromatography/mass spectrometry

✍ Scribed by Budzikiewicz, H.; Dallakian, P.; Griesbeck, A. G.; Heckroth, H.


Publisher
John Wiley and Sons
Year
1998
Tongue
English
Weight
115 KB
Volume
33
Category
Article
ISSN
1076-5174

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✦ Synopsis


The photochemistry of three N-acetoacetyl a-amino acid (valine, tert-leucine, isoleucine) methyl esters was investigated. The products after UV irradiation in acetonitrile at 300 nm (direct excitation) were analyzed by gas chromatography coupled with chemical ionization mass spectrometry. In all cases a complex product mixture was found as the result of the np* excitation of the substrates. The major reaction paths were Norrish type I reactions and hydrogen atom abstractions with concomitant radical cleavage and radical recombination steps. John