A simple route to polysubstituted benzofurans based on the domino reaction of commercial or easily available salicyl alcohols with N-protected furfurylamine has been designed and developed. The reaction was found to proceed with reasonable yields under heating of substrates in acetic acid in the presence of catalytic amount of conc. HCl when tosyl was used as protecting group. © 2017 Elsevier Lt
A convenient and efficient one-pot synthesis of benzofurans 3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, ...
The preparation of highly functionalized benzofurans by a unique and connective transformation is re...
A novel route for the synthesis of a variety of 2-trifluoromethylbenzofurans is reported. By selecti...
A simple route to polysubstituted benzofurans based on the domino reaction of commercial or easily a...
Reaction of O-arylhydroxylamine hydrochlorides with either cyclic or acyclic ketones in the presence...
An efficient, three-component strategy for the improved synthesis of multifunctionalized 6,7-dihydro...
Benzofuran itself is an oily chemical compound, extracted from coal tar, which is converted into a s...
Benzofurans are everywhere in nature and they have been extensively studied by medicinal chemists ov...
A novel copper(I)-catalyzed chemoselective reduction of the carbonyls of benzofuran-2-yl ketones ov...
Data, concerning condensation reactions of salicylaldehydes and 2-methylfuran are generalized. Durin...
An unusual Brønsted acid catalyzed benzofuran ring opening and furan ring closure sequence for the f...
A simple organocatalytic synthesis of substituted furans has been developed. The novel features of t...
A valuable Lewis-acid-catalysed domino reaction involving a Friedel–Crafts alkylation of variously s...
A convenient and efficient one-pot synthesis of benzofurans 3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, ...
Direct access to 3-trifluoromethyl-substituted benzofuranols is presented. The products are obtained...
A convenient and efficient one-pot synthesis of benzofurans 3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, ...
The preparation of highly functionalized benzofurans by a unique and connective transformation is re...
A novel route for the synthesis of a variety of 2-trifluoromethylbenzofurans is reported. By selecti...
A simple route to polysubstituted benzofurans based on the domino reaction of commercial or easily a...
Reaction of O-arylhydroxylamine hydrochlorides with either cyclic or acyclic ketones in the presence...
An efficient, three-component strategy for the improved synthesis of multifunctionalized 6,7-dihydro...
Benzofuran itself is an oily chemical compound, extracted from coal tar, which is converted into a s...
Benzofurans are everywhere in nature and they have been extensively studied by medicinal chemists ov...
A novel copper(I)-catalyzed chemoselective reduction of the carbonyls of benzofuran-2-yl ketones ov...
Data, concerning condensation reactions of salicylaldehydes and 2-methylfuran are generalized. Durin...
An unusual Brønsted acid catalyzed benzofuran ring opening and furan ring closure sequence for the f...
A simple organocatalytic synthesis of substituted furans has been developed. The novel features of t...
A valuable Lewis-acid-catalysed domino reaction involving a Friedel–Crafts alkylation of variously s...
A convenient and efficient one-pot synthesis of benzofurans 3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, ...
Direct access to 3-trifluoromethyl-substituted benzofuranols is presented. The products are obtained...
A convenient and efficient one-pot synthesis of benzofurans 3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, ...
The preparation of highly functionalized benzofurans by a unique and connective transformation is re...
A novel route for the synthesis of a variety of 2-trifluoromethylbenzofurans is reported. By selecti...