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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

a–c Reactions catalyzed by pyruvate decarboxylase (PDC). a Pyruvate... |  Download High-Quality Scientific Diagram
a–c Reactions catalyzed by pyruvate decarboxylase (PDC). a Pyruvate... | Download High-Quality Scientific Diagram

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

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

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

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

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

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

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

Enhanced production of R-phenylacetylcarbinol (R-PAC) through enzymatic  biotransformation - ScienceDirect
Enhanced production of R-phenylacetylcarbinol (R-PAC) through enzymatic biotransformation - ScienceDirect

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

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

EP1240347B1 - Yeast-based process for production of l-pac - Google Patents
EP1240347B1 - Yeast-based process for production of l-pac - Google Patents

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

Phenylacetylcarbinol - Wikiwand
Phenylacetylcarbinol - Wikiwand

L-Phenylacetylcarbinol presentation
L-Phenylacetylcarbinol presentation

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

วิธีการผลิตไพรูเวตและการนาไพรูเวตไปประยุกต
วิธีการผลิตไพรูเวตและการนาไพรูเวตไปประยุกต

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

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

Manufacturing by-products from, and stereochemical outcomes of the  biotransformation of benzaldehyde used in the synthesis of methamphetamine  - ScienceDirect
Manufacturing by-products from, and stereochemical outcomes of the biotransformation of benzaldehyde used in the synthesis of methamphetamine - ScienceDirect

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

Phenylacetylcarbinol - Wikipedia
Phenylacetylcarbinol - Wikipedia

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

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

Enzymatic (R)-phenylacetylcarbinol production in a benzaldehyde emulsion  system with Candida utilis cells | SpringerLink
Enzymatic (R)-phenylacetylcarbinol production in a benzaldehyde emulsion system with Candida utilis cells | SpringerLink

L-phenylacetylcarbinol production by yeast petite mutants | Annals of  Microbiology | Full Text
L-phenylacetylcarbinol production by yeast petite mutants | Annals of Microbiology | Full Text

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

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

Phenylacetylcarbinol - Wikipedia
Phenylacetylcarbinol - Wikipedia