TY - JOUR
T1 - An Easy Access to Benzofurans via DBU Induced Condensation Reaction of Active 2‐Hydroxy Acetophenones with Phenacyl Chlorides
T2 - A Novel Class of Antioxidant Agents
AU - Rangaswamy, J.
AU - Kumar, H. Vijay
AU - Harini, S. T.
AU - Naik, Nagaraja
N1 - Publisher Copyright:
© 2014 HeteroCorporation
PY - 2015/5
Y1 - 2015/5
N2 - A convenient and efficient one‐pot synthesis of benzofurans 3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, 3k, 3l, 3m, 3n, 3o, 3p, 3q, 3r, 3s, 3t has been described from 2‐hydroxy acetophenones and phenacyl chlorides in the presence of DBU. The procedure was applicable for a variety of phenacyl chlorides and provides a variety of benzofurans with higher yields. DBU acts as a base and as well as nucleophiles. All the derivatives were subjected to in vitro antioxidant screenings against representative 2,2′‐diphenyl‐1‐picryl‐hydrazyl and 2,2′‐azino‐bis(3‐ethylbenzthiazoline‐6‐sulfonic acid) radicals and results worth for further investigations.
AB - A convenient and efficient one‐pot synthesis of benzofurans 3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, 3k, 3l, 3m, 3n, 3o, 3p, 3q, 3r, 3s, 3t has been described from 2‐hydroxy acetophenones and phenacyl chlorides in the presence of DBU. The procedure was applicable for a variety of phenacyl chlorides and provides a variety of benzofurans with higher yields. DBU acts as a base and as well as nucleophiles. All the derivatives were subjected to in vitro antioxidant screenings against representative 2,2′‐diphenyl‐1‐picryl‐hydrazyl and 2,2′‐azino‐bis(3‐ethylbenzthiazoline‐6‐sulfonic acid) radicals and results worth for further investigations.
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U2 - 10.1002/jhet.1971
DO - 10.1002/jhet.1971
M3 - Article
AN - SCOPUS:85027921720
SN - 0022-152X
VL - 52
SP - 938
EP - 943
JO - Journal of Heterocyclic Chemistry
JF - Journal of Heterocyclic Chemistry
IS - 3
ER -