Jump to main content
Jump to site search

Issue 41, 2014
Previous Article Next Article

Molecular iodine-mediated reaction of 2-(2-phenylethynyl)-Morita–Baylis–Hillman adducts: an easy route to naphthyl ketones and iodo-substituted isochromenes

Author affiliations

Abstract

The molecular iodine-promoted reaction of 2-(2-phenylethynyl)-Morita–Baylis–Hillman adducts is reported. In the presence of I2, naphthyl ketone derivatives are produced, whereas in the presence of I2/K3PO4, iodo-substituted isochromene derivatives are produced.

Graphical abstract: Molecular iodine-mediated reaction of 2-(2-phenylethynyl)-Morita–Baylis–Hillman adducts: an easy route to naphthyl ketones and iodo-substituted isochromenes

Back to tab navigation

Supplementary files

Article information


Submitted
07 May 2014
Accepted
13 Aug 2014
First published
13 Aug 2014

Org. Biomol. Chem., 2014,12, 8247-8256
Article type
Paper
Author version available

Molecular iodine-mediated reaction of 2-(2-phenylethynyl)-Morita–Baylis–Hillman adducts: an easy route to naphthyl ketones and iodo-substituted isochromenes

D. Janreddy, V. Kavala, T. Kotipalli, R. R. Rajawinslin, C. Kuo, W. Huang and C. Yao, Org. Biomol. Chem., 2014, 12, 8247
DOI: 10.1039/C4OB00938J

Social activity

Search articles by author

Spotlight

Advertisements