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Addition of alkyl radicals, generated from carboxylic acids via photochemical decarboxylation, to glyoxylic oxime ether: a mild and efficient route to α-substituted α-aminoesters

✍ Scribed by Yasuharu Yoshimi; Kosuke Kobayashi; Hayato Kamakura; Keisuke Nishikawa; Yoshiki Haga; Kousuke Maeda; Toshio Morita; Tatsuya Itou; Yutaka Okada; Minoru Hatanaka


Publisher
Elsevier Science
Year
2010
Tongue
French
Weight
505 KB
Volume
51
Category
Article
ISSN
0040-4039

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✦ Synopsis


Radical addition to a glyoxylic oxime ether was accomplished under mild conditions using an alkyl radical generated from a free carboxylic acid via photochemical decarboxylation. The photoreaction provided an efficient route to a-substituted a-aminoesters from carboxylic acids and oxime ether.


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