Issue 4, 1990

Photocyclization of (ω-dialkylamino)alkyl β-oxoesters via remote hydrogen transfer

Abstract

The (ω-dialkylamino)alkyl β-oxoesters (1) undergo photocyclization via remote hydrogen transfer to give the medium-sized azalactones (2) and/or aminolactones (3). Intramolecular electron transfer from nitrogen to the excited carbonyl group of (1) occurs prior to the remote hydrogen transfer.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1990, 901-905

Photocyclization of (ω-dialkylamino)alkyl β-oxoesters via remote hydrogen transfer

T. Hasegawa, T. Ogawa, K. Miyata, A. Karakizawa, M. Komiyama, K. Nishizawa and M. Yoshioka, J. Chem. Soc., Perkin Trans. 1, 1990, 901 DOI: 10.1039/P19900000901

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