Current affiliation: Niigata UniversitySubject: ChemistryPrimary location: Japan
Published in:Organic & Biomolecular ChemistryPublication date:2012-01-01
Published in:Chemical CommunicationsPublication date:2014-01-01
The base-induced asymmetric [2,3] Stevens rearrangement of N-cinnamyl tetraalkylammonium ylides derived from L-alanine amides that proceeds via a d...
Published in:Chemical CommunicationsPublication date:2008-01-01
Published in:Angewandte Chemie International EditionPublication date:2007-11-26
Published in:Organic & Biomolecular ChemistryPublication date:2008-01-01
Published in:TetrahedronPublication date:2010-11-01
Published in:Tetrahedron LettersPublication date:2012-03-01
Published in:HeterocyclesPublication date:2013-01-01
Published in:HeterocyclesPublication date:2005-01-01
Published in:Chemical CommunicationsPublication date:2016-01-01
The base-promoted [1,4] Wittig rearrangement of alkyl allylic ethers to generate enolates is a unique transformation in organic synthesis; however,...
Published in:HeterocyclesPublication date:2016-01-01
Published in:European Journal of Organic ChemistryPublication date:2010-11-02
Published in:European Journal of Organic ChemistryPublication date:2016-06-27
Ring-Strain Effects in Base-Induced Sommelet-Hauser Rearrangement: Application to Successive Stereocontrolled Transformations
The reaction proceeded in good yield to afford the desired alpha-aryl azetidinic acid esters without any detectable amount of the competitive [1,2]...
Published in:Organic & Biomolecular ChemistryPublication date:2018-01-01
The dearomative [2,3] sigmatropic rearrangement followed by 1,4-elimination of ammonium ylides to provide alpha-(ortho-vinylphenyl)amino acid ester...
Published in:Organic & Biomolecular ChemistryPublication date:2017-01-01