The hindered nonionic phosphazene base P4-t-Bu efficiently deprotonates o-arylmethoxy benzaldehydes, leading to a direct synthesis of benzofurans. Strong ionic bases such as LDA, LiTMP, and KH failed
© The Royal Society of Chemistry 2020. An expedient synthesis of highly substituted tetrahydrobenzof...
A novel, convenient procedure has been described for the construction of fluorine-containing benzaze...
Palladium-catalyzed oxidative annulations between phenols and alkenylcarboxylic acids produced a lib...
The hindered nonionic phosphazene base P4-t-Bu efficiently deprotonates o-arylmethoxy benzaldehydes,...
The 19th International Electronic Conference on Synthetic Organic Chemistry session General Organic ...
3-Benzoyl[b]benzofurans are structural cores to a host of bioactive molecules in pharmaceutical use ...
A convenient and efficient one-pot synthesis of benzofurans 3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, ...
A convenient and efficient one-pot synthesis of benzofurans 3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, ...
The reaction of o-acyloxybenzylidenetriphenylphosphoranes with substituted benzoyl chlorides in an a...
Reaction of O-arylhydroxylamine hydrochlorides with either cyclic or acyclic ketones in the presence...
This review describes the progress of the last decade on the synthesis of substituted benzofurans, w...
A novel type of deprotonative functionalization of aromatics was accomplished with a phosphazene bas...
In the last years we largely investigated a method for oxy-functionalize the aromatic ring of natura...
This thesis describes the synthesis of bioactive benzofuran compounds using the halogen-metal exchan...
An efficient methodology for the synthesis of benzofuropyridines and dibenzofurans from fluoropyridi...
© The Royal Society of Chemistry 2020. An expedient synthesis of highly substituted tetrahydrobenzof...
A novel, convenient procedure has been described for the construction of fluorine-containing benzaze...
Palladium-catalyzed oxidative annulations between phenols and alkenylcarboxylic acids produced a lib...
The hindered nonionic phosphazene base P4-t-Bu efficiently deprotonates o-arylmethoxy benzaldehydes,...
The 19th International Electronic Conference on Synthetic Organic Chemistry session General Organic ...
3-Benzoyl[b]benzofurans are structural cores to a host of bioactive molecules in pharmaceutical use ...
A convenient and efficient one-pot synthesis of benzofurans 3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, ...
A convenient and efficient one-pot synthesis of benzofurans 3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, ...
The reaction of o-acyloxybenzylidenetriphenylphosphoranes with substituted benzoyl chlorides in an a...
Reaction of O-arylhydroxylamine hydrochlorides with either cyclic or acyclic ketones in the presence...
This review describes the progress of the last decade on the synthesis of substituted benzofurans, w...
A novel type of deprotonative functionalization of aromatics was accomplished with a phosphazene bas...
In the last years we largely investigated a method for oxy-functionalize the aromatic ring of natura...
This thesis describes the synthesis of bioactive benzofuran compounds using the halogen-metal exchan...
An efficient methodology for the synthesis of benzofuropyridines and dibenzofurans from fluoropyridi...
© The Royal Society of Chemistry 2020. An expedient synthesis of highly substituted tetrahydrobenzof...
A novel, convenient procedure has been described for the construction of fluorine-containing benzaze...
Palladium-catalyzed oxidative annulations between phenols and alkenylcarboxylic acids produced a lib...