Cholic and deoxycholic acids were found to form inclusion compounds with various racemic cyclic ketones enabling direct and straightforward enantiomer separation. The X-ray structure of the 2:1 inclusion complex between (-)-bicyclo[3.2.0]-hept-2-en-6-one and cholic acid is reported. © 2001 Elsevier Science Ltd. All rights reserved.
Enantioselective inclusion in bile acids: Resolution of cyclic ketones
BERTOLASI, Valerio;BORTOLINI, Olga;FOGAGNOLO, Marco;FANTIN, Giancarlo;PEDRINI, Paola
2001
Abstract
Cholic and deoxycholic acids were found to form inclusion compounds with various racemic cyclic ketones enabling direct and straightforward enantiomer separation. The X-ray structure of the 2:1 inclusion complex between (-)-bicyclo[3.2.0]-hept-2-en-6-one and cholic acid is reported. © 2001 Elsevier Science Ltd. All rights reserved.File in questo prodotto:
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