TY - JOUR
T1 - Molecular iodine-mediated reaction of 2-(2-phenylethynyl)-Morita-Baylis-Hillman adducts
T2 - An easy route to naphthyl ketones and iodo-substituted isochromenes
AU - Janreddy, Donala
AU - Kavala, Veerababurao
AU - Kotipalli, Trimurtulu
AU - Rajawinslin, R. R.
AU - Kuo, Chun Wei
AU - Huang, Wen Chang
AU - Yao, Ching Fa
PY - 2014/11/7
Y1 - 2014/11/7
N2 - 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. This journal is
AB - 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. This journal is
UR - http://www.scopus.com/inward/record.url?scp=84907646518&partnerID=8YFLogxK
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U2 - 10.1039/c4ob00938j
DO - 10.1039/c4ob00938j
M3 - Article
C2 - 25203199
AN - SCOPUS:84907646518
VL - 12
SP - 8247
EP - 8256
JO - Organic and Biomolecular Chemistry
JF - Organic and Biomolecular Chemistry
SN - 1477-0520
IS - 41
ER -