ISBN: 9783845407586

Heterogeneous asymmetric catalysis remains as an exciting research field in chiral catalysis since the heterogeneous catalyst can be separated easily from the reaction mixture compare to … More...

Heterogeneous asymmetric catalysis remains as an exciting research field in chiral catalysis since the heterogeneous catalyst can be separated easily from the reaction mixture compare to conventional homogeneous catalyst. The aim of the research is to develop and investigate a novel heterogeneous asymmetric catalyst using amino acid as chiral promoter. The catalysts were synthesized by attachment of amino acids such as L-glutamic acid, L-leucine and L-phenylalanine onto the hydrophilic part of hydrolyzed octadecyltrichlorosilane (OTS). The amino acidhydrolyzed OTS materials were used as catalysts for the asymmetric hydration of epoxycyclohexene to yield two diastereoisomers, namely (1R,2R)-trans-1,2-cyclohexanediol, (1S,2S)-trans-1,2-cyclohexanediol and cis-1,2-cyclohexanediol. Bücher > Fremdsprachige Bücher > Englische Bücher 220 x 150 x 6 mm , LAP LAMBERT Academic Publishing, Taschenbuch, LAP LAMBERT Academic Publishing<

2011, ISBN: 9783845407586

Heterogeneous asymmetric catalysis remains as an exciting research field in chiral catalysis since the heterogeneous catalyst can be separated easily from the reaction mixture compare to … More...

Heterogeneous asymmetric catalysis remains as an exciting research field in chiral catalysis since the heterogeneous catalyst can be separated easily from the reaction mixture compare to conventional homogeneous catalyst. The aim of the research is to develop and investigate a novel heterogeneous asymmetric catalyst using amino acid as chiral promoter. The catalysts were synthesized by attachment of amino acids such as L-glutamic acid, L-leucine and L-phenylalanine onto the hydrophilic part of hydrolyzed octadecyltrichlorosilane (OTS). The amino acidhydrolyzed OTS materials were used as catalysts for the asymmetric hydration of epoxycyclohexene to yield two diastereoisomers, namely (1R,2R)-trans-1,2-cyclohexanediol, (1S,2S)-trans-1,2-cyclohexanediol and cis-1,2-cyclohexanediol. Buch (fremdspr.) Hadi Nur#Lim Kheng Wei Taschenbuch, LAP LAMBERT Academic Publishing, 04.07.2011, LAP LAMBERT Academic Publishing, 2011<

ISBN: 9783845407586

Paperback, [PU: LAP LAMBERT Academic Publishing], Heterogeneous asymmetric catalysis remains as an exciting research field in chiral catalysis since the heterogeneous catalyst can be sepa… More...

Paperback, [PU: LAP LAMBERT Academic Publishing], Heterogeneous asymmetric catalysis remains as an exciting research field in chiral catalysis since the heterogeneous catalyst can be separated easily from the reaction mixture compare to conventional homogeneous catalyst. The aim of the research is to develop and investigate a novel heterogeneous asymmetric catalyst using amino acid as chiral promoter. The catalysts were synthesized by attachment of amino acids such as L-glutamic acid, L-leucine and L-phenylalanine onto the hydrophilic part of hydrolyzed octadecyltrichlorosilane (OTS). The amino acidhydrolyzed OTS materials were used as catalysts for the asymmetric hydration of epoxycyclohexene to yield two diastereoisomers, namely (1R,2R)-trans-1,2-cyclohexanediol, (1S,2S)-trans-1,2-cyclohexanediol and cis-1,2-cyclohexanediol., Chemistry<

ISBN: 9783845407586

Paperback, [PU: LAP Lambert Academic Publishing], Heterogeneous asymmetric catalysis remains as an exciting research field in chiral catalysis since the heterogeneous catalyst can be sepa… More...

Paperback, [PU: LAP Lambert Academic Publishing], Heterogeneous asymmetric catalysis remains as an exciting research field in chiral catalysis since the heterogeneous catalyst can be separated easily from the reaction mixture compare to conventional homogeneous catalyst. The aim of the research is to develop and investigate a novel heterogeneous asymmetric catalyst using amino acid as chiral promoter. The catalysts were synthesized by attachment of amino acids such as L-glutamic acid, L-leucine and L-phenylalanine onto the hydrophilic part of hydrolyzed octadecyltrichlorosilane (OTS). The amino acidhydrolyzed OTS materials were used as catalysts for the asymmetric hydration of epoxycyclohexene to yield two diastereoisomers, namely (1R,2R)-trans-1,2-cyclohexanediol, (1S,2S)-trans-1,2-cyclohexanediol and cis-1,2-cyclohexanediol., Chemistry<

2011, ISBN: 3845407581

Kartoniert / Broschiert, mit Schutzumschlag 11, [PU:LAP LAMBERT Academic Publishing]