![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](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs00253-014-5635-5/MediaObjects/253_2014_5635_Fig1_HTML.gif)
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](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs00253-014-5635-5/MediaObjects/253_2014_5635_Fig3_HTML.gif)
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](https://ars.els-cdn.com/content/image/1-s2.0-S0379073813005185-sc2.jpg)
Investigation of the l-phenylacetylcarbinol process to substituted benzaldehydes of interest - ScienceDirect
![Figure 1 from Screening of Yeasts for Cell-Free Production of (R)- Phenylacetylcarbinol in a Shake Flask Condition | Semantic Scholar Figure 1 from Screening of Yeasts for Cell-Free Production of (R)- Phenylacetylcarbinol in a Shake Flask Condition | Semantic Scholar](https://d3i71xaburhd42.cloudfront.net/027b584b9c79f32924aa86b59f5c4f9c36afdf8a/2-Figure1-1.png)
Figure 1 from Screening of Yeasts for Cell-Free Production of (R)- Phenylacetylcarbinol in a Shake Flask Condition | Semantic Scholar
![Production of Ethanol and R-phenylacetylcarbinol from Whole Cell Biocatalyst Utilizes Carbon Source from Dried Longan Amalia S. Agustina, Poonsiri Phrathong, - ppt download Production of Ethanol and R-phenylacetylcarbinol from Whole Cell Biocatalyst Utilizes Carbon Source from Dried Longan Amalia S. Agustina, Poonsiri Phrathong, - ppt download](https://slideplayer.com/8421159/26/images/slide_1.jpg)
Production of Ethanol and R-phenylacetylcarbinol from Whole Cell Biocatalyst Utilizes Carbon Source from Dried Longan Amalia S. Agustina, Poonsiri Phrathong, - ppt download
Sciencemadness Discussion Board - Synthesis of Phenylacetylcarbinol by Alkyne Hydration and Subsequent Enamine formation - Powered by XMB 1.9.11
![Biotransformation of benzaldehyde to L‐phenylacetylcarbinol (L‐PAC) by Torulaspora delbrueckii and conversion to ephedrine by microwave radiation - Shukla - 2002 - Journal of Chemical Technology & Biotechnology - Wiley Online Library Biotransformation of benzaldehyde to L‐phenylacetylcarbinol (L‐PAC) by Torulaspora delbrueckii and conversion to ephedrine by microwave radiation - Shukla - 2002 - Journal of Chemical Technology & Biotechnology - Wiley Online Library](https://onlinelibrary.wiley.com/cms/asset/f6e0759f-3454-43e3-a782-df2dce8def3b/mfig001.jpg)
Biotransformation of benzaldehyde to L‐phenylacetylcarbinol (L‐PAC) by Torulaspora delbrueckii and conversion to ephedrine by microwave radiation - Shukla - 2002 - Journal of Chemical Technology & Biotechnology - Wiley Online Library
![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](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs00253-014-5635-5/MediaObjects/253_2014_5635_Fig4_HTML.gif)
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](https://media.springernature.com/lw685/springer-static/image/art%3A10.1007%2Fs00253-005-0063-1/MediaObjects/253_2005_63_Fig1_HTML.gif)
Enzymatic (R)-phenylacetylcarbinol production in a benzaldehyde emulsion system with Candida utilis cells | 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](https://ars.els-cdn.com/content/image/1-s2.0-S0379073813005185-sc1.jpg)