Issue 0, 1972

Experiments on the synthesis of tetracyclines. Part XII. Extension of the acetal photocyclisation process

Abstract

In analogy to earlier work, the acid-catalysed photocyclisation of 3-[2-(dioxolan-2-yl)benzyl]chromone (II; XX = O·CH2·CH2·O) to give 6,6-ethylenedioxy-5aα6,11,11aα-tetrahydro-12H-benzo[b]xanthen-12-one (III) and its trans-(5aαH,11aβH)isomer (IV) has been effected. It is suggested that this photocyclisation process will be of general synthetic utility.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1972, 1103-1105

Experiments on the synthesis of tetracyclines. Part XII. Extension of the acetal photocyclisation process

D. H. R. Barton, P. D. Magnus and J. I. Okogun, J. Chem. Soc., Perkin Trans. 1, 1972, 1103 DOI: 10.1039/P19720001103

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