E. V. Buravlev, I. Chukicheva, A. V. Churakov
Feb 15, 2012
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0
Influential Citations
4
Citations
Journal
Russian Journal of Organic Chemistry
Abstract
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.