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EP1421055B1 - Methods for the synthesis of amines such as ephedrine and  intermediates - Google Patents
EP1421055B1 - Methods for the synthesis of amines such as ephedrine and intermediates - Google Patents

An N-methyltransferase from Ephedra sinica catalyzing the formation of  ephedrine and pseudoephedrine enables microbial phenylalkylamine production  - Journal of Biological Chemistry
An N-methyltransferase from Ephedra sinica catalyzing the formation of ephedrine and pseudoephedrine enables microbial phenylalkylamine production - Journal of Biological Chemistry

Biotransformation of benzaldehyde to L‐phenylacetylcarbinol (L‐PAC) by  Torulaspora delbrueckii and conversion to ephedrine by microwave radiation  | Semantic Scholar
Biotransformation of benzaldehyde to L‐phenylacetylcarbinol (L‐PAC) by Torulaspora delbrueckii and conversion to ephedrine by microwave radiation | Semantic Scholar

Validation of mathematical model with phosphate activation effect by batch  (R)-phenylacetylcarbinol biotransformation process utilizing Candida  tropicalis pyruvate decarboxylase in phosphate buffer | Scientific Reports
Validation of mathematical model with phosphate activation effect by batch (R)-phenylacetylcarbinol biotransformation process utilizing Candida tropicalis pyruvate decarboxylase in phosphate buffer | Scientific Reports

Potential of some yeast strains in the stereoselective synthesis of (R)-(−)- phenylacetylcarbinol and (S)-(+)-phenylacetylcarbinol and their reduced  1,2-dialcohol derivatives | SpringerLink
Potential of some yeast strains in the stereoselective synthesis of (R)-(−)- phenylacetylcarbinol and (S)-(+)-phenylacetylcarbinol and their reduced 1,2-dialcohol derivatives | SpringerLink

US7176332B2 - Methods for the synthesis of amines such as ephedrine and  intermediates - Google Patents
US7176332B2 - Methods for the synthesis of amines such as ephedrine and intermediates - Google Patents

Phenylacetylcarbinol - Wikipedia
Phenylacetylcarbinol - Wikipedia

Asymmetric synthesis of ( S )-phenylacetylcarbinol – closing a gap in C–C  bond formation - Green Chemistry (RSC Publishing) DOI:10.1039/C6GC01803C
Asymmetric synthesis of ( S )-phenylacetylcarbinol – closing a gap in C–C bond formation - Green Chemistry (RSC Publishing) DOI:10.1039/C6GC01803C

Potential of some yeast strains in the stereoselective synthesis of (R)-(−)- phenylacetylcarbinol and (S)-(+)-phenylacetylcarbinol and their reduced  1,2-dialcohol derivatives | SpringerLink
Potential of some yeast strains in the stereoselective synthesis of (R)-(−)- phenylacetylcarbinol and (S)-(+)-phenylacetylcarbinol and their reduced 1,2-dialcohol derivatives | SpringerLink

Selection of Yeasts for the Production of L-phenyl-acetil- carbinol  Bybiotransformation in Shake Flasks
Selection of Yeasts for the Production of L-phenyl-acetil- carbinol Bybiotransformation in Shake Flasks

Synthesis of novel β-amino alcohols from phenylacetylcarbinol: cytotoxicity  activity against A549 cells and molecular docking | SpringerLink
Synthesis of novel β-amino alcohols from phenylacetylcarbinol: cytotoxicity activity against A549 cells and molecular docking | SpringerLink

Phenylacetylcarbinol - Wikipedia
Phenylacetylcarbinol - Wikipedia

Synthesis of R-(−)-phenylacetylcarbinol by fermenting yeast and... |  Download High-Resolution Scientific Diagram
Synthesis of R-(−)-phenylacetylcarbinol by fermenting yeast and... | Download High-Resolution Scientific Diagram

The production of ephedrine and pseudoephedrine from ( R )PAC: ( R... |  Download Scientific Diagram
The production of ephedrine and pseudoephedrine from ( R )PAC: ( R... | Download Scientific Diagram

Raney-nickel-iron catalyst, its preparation and a method to produce  L-norephedrine by hydrogenating L-phenylacetylcarbinol-oxime with said  catalyst - Patent 2055379
Raney-nickel-iron catalyst, its preparation and a method to produce L-norephedrine by hydrogenating L-phenylacetylcarbinol-oxime with said catalyst - Patent 2055379

Improvement of the yeast based (R)-phenylacetylcarbinol production process  via reduction of by-product formation - ScienceDirect
Improvement of the yeast based (R)-phenylacetylcarbinol production process via reduction of by-product formation - ScienceDirect

DE60226038T2 - PROCESS FOR SYNTHESIS OF AMINES SUCH AS EPHEDRINE AND  INTERMEDIATE PRODUCTS - Google Patents
DE60226038T2 - PROCESS FOR SYNTHESIS OF AMINES SUCH AS EPHEDRINE AND INTERMEDIATE PRODUCTS - Google Patents

Sciencemadness Discussion Board - Synthesis of Phenylacetylcarbinol by  Alkyne Hydration and Subsequent Enamine formation - Powered by XMB 1.9.11
Sciencemadness Discussion Board - Synthesis of Phenylacetylcarbinol by Alkyne Hydration and Subsequent Enamine formation - Powered by XMB 1.9.11

Reductive Amination in the Synthesis of Pharmaceuticals | Chemical Reviews
Reductive Amination in the Synthesis of Pharmaceuticals | Chemical Reviews

Potential of some yeast strains in the stereoselective synthesis of (R)-(−)- phenylacetylcarbinol and (S)-(+)-phenylacetylcarbinol and their reduced  1,2-dialcohol derivatives | SpringerLink
Potential of some yeast strains in the stereoselective synthesis of (R)-(−)- phenylacetylcarbinol and (S)-(+)-phenylacetylcarbinol and their reduced 1,2-dialcohol derivatives | SpringerLink

Investigation of the l-phenylacetylcarbinol process to substituted  benzaldehydes of interest - ScienceDirect
Investigation of the l-phenylacetylcarbinol process to substituted benzaldehydes of interest - ScienceDirect

Catalytic Cycle of Rhodium-Catalyzed Asymmetric 1,4-Addition of  Organoboronic Acids. Arylrhodium, Oxa-π-allylrhodium, and Hydroxorhodium  Intermediates | Journal of the American Chemical Society
Catalytic Cycle of Rhodium-Catalyzed Asymmetric 1,4-Addition of Organoboronic Acids. Arylrhodium, Oxa-π-allylrhodium, and Hydroxorhodium Intermediates | Journal of the American Chemical Society

L-Phenylacetylcarbinol presentation
L-Phenylacetylcarbinol presentation

US20090112025A1 - Catalytic hydrogenation process and novel catalyst for it  - Google Patents
US20090112025A1 - Catalytic hydrogenation process and novel catalyst for it - Google Patents

Mechanistic study of the biosynthesis of R-phenylacetylcarbinol by  acetohydroxyacid synthase enzyme using hybrid quantum mechanics/molecular  mechanics simulations - ScienceDirect
Mechanistic study of the biosynthesis of R-phenylacetylcarbinol by acetohydroxyacid synthase enzyme using hybrid quantum mechanics/molecular mechanics simulations - ScienceDirect

US7176332B2 - Methods for the synthesis of amines such as ephedrine and  intermediates - Google Patents
US7176332B2 - Methods for the synthesis of amines such as ephedrine and intermediates - Google Patents

Synthesis of Chiral Catalyst Modifiers by Hydrosilylation of Cinchonidine  and Their Application in the Hydrogenation of 1‐Phenylpropane‐1,2‐dione and  Ethyl Pyruvate on a Supported Pt/Al2O3 Catalyst - Busygin - 2005 - European  Journal
Synthesis of Chiral Catalyst Modifiers by Hydrosilylation of Cinchonidine and Their Application in the Hydrogenation of 1‐Phenylpropane‐1,2‐dione and Ethyl Pyruvate on a Supported Pt/Al2O3 Catalyst - Busygin - 2005 - European Journal