1358613-89-4Relevant academic research and scientific papers
Optical resolution of racemic 4-hydroxy-3-isobornyl-5-methylbenzaldehyde
Buravlev,Yu Chukicheva,Churakov,Kutchin
, p. 64 - 68 (2012/05/20)
Racemic 4-hydroxy-3-isobornyl-5-methylbenzaldehyde was separated into particular enantiomers via transformation into diastereoisomeric Schiff bases by reaction with (R)-1-phenylethanamine. The absolute configuration of the products was determined on the basis of the X-ray diffraction data for camphanate derived from one enantiomer of 4-hydroxy-3-isobornyl-5- methylbenzaldehyde. Pleiades Publishing, Ltd., 2012.
