Regio- and stereoselective addition of alkyl Grignard reagents to pyridine-N-oxides gave C2-alkylated N-hydroxy-1,2,5,6-tetrahydropyridines and trans-2,3-disubstituted N-hydroxy-1,2,5,6-tetrahydropyridines in good to excellent yields. These intermediates were aromatized or alternatively reduced in one-pot methodologies for efficient syntheses of alkylpyridines or piperidines, respectively. These reactions have a broad substrate scope and short reaction times.</p
The synthesis of optically active piperidines by enantioselective addition of aryl Grignard reagents...
Reported herein is an unprecedented base-promoted deborylative alkylation of pyridine N-oxides using...
Diastereoselective epoxidation and regioselective ring-opening methods were developed for the synthe...
Regio- and stereoselective addition of alkyl Grignard reagents to pyridine-N-oxides gave C2-alkylate...
Regio- and stereoselective addition of alkyl Grignard reagents to pyridine-N-oxides gave C2-alkylate...
Regio- and stereoselective addition of alkyl Grignard reagents to pyridine-N-oxides gave C2-alkylate...
Regio- and stereoselective addition of alkyl Grignard reagents to pyridine-<i>N</i>-oxides gave C2-a...
This thesis describes the development of new synthetic methodologies for preparation of bioactive in...
This thesis describes the development of new synthetic methodologies for preparation of bioactive in...
This thesis describes the development of new synthetic methodologies for preparation of bioactive in...
The unprecedented substitution of a nitro group with aryl or alkenyl groups of Grignard reagents aff...
A regioselective synthesis of pyridines by the addition of malonate anions to pyridine N-oxide deriv...
The first example of C alkylation of 1,2-dihydropyridines with alkyl triflates and Michael acceptors...
A facile arylation, alkenylation, and alkylation of functionalized 2-halopyridine <i>N</i>-oxides wi...
Treatment of salts 1a?b with Grignard reagents gives, after reduction of the resulting unstable dih...
The synthesis of optically active piperidines by enantioselective addition of aryl Grignard reagents...
Reported herein is an unprecedented base-promoted deborylative alkylation of pyridine N-oxides using...
Diastereoselective epoxidation and regioselective ring-opening methods were developed for the synthe...
Regio- and stereoselective addition of alkyl Grignard reagents to pyridine-N-oxides gave C2-alkylate...
Regio- and stereoselective addition of alkyl Grignard reagents to pyridine-N-oxides gave C2-alkylate...
Regio- and stereoselective addition of alkyl Grignard reagents to pyridine-N-oxides gave C2-alkylate...
Regio- and stereoselective addition of alkyl Grignard reagents to pyridine-<i>N</i>-oxides gave C2-a...
This thesis describes the development of new synthetic methodologies for preparation of bioactive in...
This thesis describes the development of new synthetic methodologies for preparation of bioactive in...
This thesis describes the development of new synthetic methodologies for preparation of bioactive in...
The unprecedented substitution of a nitro group with aryl or alkenyl groups of Grignard reagents aff...
A regioselective synthesis of pyridines by the addition of malonate anions to pyridine N-oxide deriv...
The first example of C alkylation of 1,2-dihydropyridines with alkyl triflates and Michael acceptors...
A facile arylation, alkenylation, and alkylation of functionalized 2-halopyridine <i>N</i>-oxides wi...
Treatment of salts 1a?b with Grignard reagents gives, after reduction of the resulting unstable dih...
The synthesis of optically active piperidines by enantioselective addition of aryl Grignard reagents...
Reported herein is an unprecedented base-promoted deborylative alkylation of pyridine N-oxides using...
Diastereoselective epoxidation and regioselective ring-opening methods were developed for the synthe...