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Volumn , Issue 12, 2009, Pages 1863-1886

En route to new chiral ferrocene derivatives: Dead ends, detours, and avenues

Author keywords

Amino alcohols; Asymmetric catalysis; Epoxides; Ferrocenes; Palladacycles

Indexed keywords

3 FERROCENYLPROP 2 ENOATE; 4 FERROCENYL 1,3 OXAZOLINE; ALPHA FERROCENYL EPOXIDE; FERROCENE DERIVATIVE; HYDROXYL GROUP; NITROGEN; NUCLEOPHILE; PALLADIUM; UNCLASSIFIED DRUG;

EID: 67651211316     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0029-1217514     Document Type: Review
Times cited : (14)

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    • As far as we are aware, the only reference concerning β-amino-β-ferrocenyl carbonyl derivatives describes the low-yield (15%) formation of rac-4-ferrocenyl-4-(2-naphthyl)aminobutanone in the reaction between (2-naphthyl)ferrocenylimine and acetone catalyzed by p-toluenesulfonic acid. See: Kalenikov, E. A. Zh. Obshch. Khim. 1977, 43, 628.
    • As far as we are aware, the only reference concerning β-amino-β-ferrocenyl carbonyl derivatives describes the low-yield (15%) formation of rac-4-ferrocenyl-4-(2-naphthyl)aminobutanone in the reaction between (2-naphthyl)ferrocenylimine and acetone catalyzed by p-toluenesulfonic acid. See: Kalenikov, E. A. Zh. Obshch. Khim. 1977, 43, 628.
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    • When, under the same reaction conditions, the p-methoxy- phenylimine of benzaldehyde was reacted with butanone, a 1:1.2 mixture of diastereomers (linear/branched) was obtained.
    • When, under the same reaction conditions, the p-methoxy- phenylimine of benzaldehyde was reacted with butanone, a 1:1.2 mixture of diastereomers (linear/branched) was obtained.


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