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Addition of lactate-derived chiral allyltrichlorostannanes to chiral aldehydes
(Pergamon-elsevier Science LtdOxfordInglaterra, 2004)
A comparative study on asymmetric reduction of ketones using the growing and resting cells of marine-derived fungi
(2018-02-01)
Whole-cell biocatalysts offer a highly enantioselective, minimally polluting route to optically active alcohols. Currently, most of the whole-cell catalytic performance involves resting cells rather than growing cell ...
Total Synthesis and Structural Validation of Phosdiecin A via Asymmetric Alcohol-Mediated Carbonyl Reductive Coupling
(American Chemical Society, 2019-09-21)
The first total synthesis and structural validation of phosdiecin A was accomplished in 13 steps through asymmetric iridium-catalyzed alcohol-mediated carbonyl reductive coupling. The present route is the shortest among ...
Asymmetric ketone reduction by immobilized Rhodotorula mucilaginosa
(2018-04-19)
In our previous study, Rhodotorula mucilaginosa (R. mucilaginosa) was selected via high throughput screening as a very active and selective whole-cell biocatalyst for the asymmetric reduction of ketones. In this study, the ...
Immobilized and free cells of geotrichum candidum for asymmetric reduction of ketones: Stability and recyclability
(2018-08-27)
Marine-derived fungus Geotrichum candidum AS 2.361 was previously reported by our group as an active strain for the enantioselective reduction of ketones. Although some other Geotrichum strains were also found from the ...
The asymmetric synthesis of (+)-sitophilure, the natural form of the aggregation pheromone of Sitophilus oryzae L-and Sitophilus zeamais M.
(Soc Brasileira QuimicaSao PauloBrasil, 1999)
Regio- and enantioselective reduction of a alpha-methyleneketone by Rhodotorula glutinis
(Arkat Usa IncGainesvilleEUA, 2003)
BAKERS-YEAST REDUCTION OF ALPHA-HALOACETOPHENONES
(Pergamon-elsevier Science LtdOxfordInglaterra, 1991)
The asymmetric synthesis of (+)-sitophilure, the natural form of the aggregation pheromone of Sitophilus oryzae L. and Sitophilus zeamais M.
(Sociedade Brasileira de Química, 1999)
Asymmetric reduction of prochiral ketones using 6 in situ generated oxazaborolidine derived from (1S,2S,3R,4R)-3-amino-7,7-dimethoxynorbornan-2-ol. An efficient synthesis of enantiopure (R)-tomoxetine
(Pergamon-elsevier Science LtdOxfordInglaterra, 2005)