578020-31-2Relevant academic research and scientific papers
Regio- and stereo-selectively kinetic resolution of four stereoisomers of 1-phenylbutan-1,3-diol by Candida rugosa lipase
Chen, Yi-Hui,Joly,Huang, Pin-Mei,Sung, Kuangsen
, p. 1031 - 1035 (2007/10/03)
Regio- and stereo-selective Candida rugosa lipase (CRL)-catalyzed acetylations of (±)-syn-1-phenylbutan-1,3-diols ((±)-syn-1) generated two monoacetates, (+)-syn-2 and (-)-syn-3, whereas that of (±)-anti-1 produced a monoacetate, (+)-anti-3, and an unreacted (-)-anti-1.
Enzyme-mediated preparation of chiral 1,3-dioxane odorants
Abate, Agnese,Brenna, Elisabetta,Fronza, Giovanni,Fuganti, Claudio,Ronzani, Sabrina,Serra, Stefano
, p. 592 - 606 (2007/10/03)
The enantiomerically enriched diastereoisomers of the chiral 1,3-dioxane odorants Floropal (1) and Magnolan (2) were prepared by an enzyme-mediated approach. Their olfactory properties were evaluated to investigate differences in the odor perception for the stereoisomers.
