Diastereoselective formation of chiral 2
โ
Jacek Gawronski; Krystyna Gawronska; Andrzej Katrusiak*
๐
Article
๐
1989
๐
Elsevier Science
๐
French
โ 614 KB
Condensation of optically active ketones, (3R)-methylcyclohexanone and 5~ cholestan-3-one. with 2-hydroxy-1-naphthaldehxde\* brings about formation of chiral 2,2'-spirobiben~d]chromene derivatives with diktertoselectivity 75% and lOO%, respectively. Absolute configuration of the newly formed chiral