78140-91-7Relevant academic research and scientific papers
Biocatalytic preparation and absolute configuration of enantiomerically pure fungistatic anti-2-benzylindane derivatives. Study of the detoxification mechanism by Botrytis cinerea
Pinedo-Rivilla, Cristina,Aleu, Josefina,Grande Benito, Manuel,Collado, Isidro G.
experimental part, p. 3784 - 3789 (2010/09/06)
Enantiomerically pure 2-benzylindane derivatives were prepared using biocatalytic methods and their absolute configuration determined. (1R,2S)-2-Benzylindan-1-ol ((1R,2S)-2) and (S)-2-benzylindan-1-one ((S)-3) were produced by fermenting baker's yeast. Li
Stereospecificity of Introduction of Hydride Ion during Double Bond Reduction of 2-Benzylidene-1-tetralone and Other Related Compounds
Chatterjee, Amareshwar,Dutta, Lakshmi N.,Chatterjee, Swapan K.
, p. 955 - 960 (2007/10/02)
Lithium aluminium hydride reduction of the benzylidene derivatives (1a-c) and (5) in refluxing THF is shown to be stereospecific, the saturated alcohol isolated in each case having the trans-stereochemistry.The benzyl ketones (30a, b, d) and (7) on sodium
