Structural and stereochemical aspects of the enantioselective halogenation of 1,3-dicarbonyl compounds catalyzed by Ti(TADDOLato) complexes

Tetrahedron

Volumn 62, Issue 30, 2006, Pages 7180-7190

  Perseghini, Mauro ^a   Massaccesi, Massimo ^a   Liu, Yanyun ^a   Togni, Antonio ^a  

^a ETH ZURICH   (Switzerland)

Author keywords

Acyl lactams; Absolute configuration; Catalytic fluorination; Ti(TADDOLato) complexes

Indexed keywords

CARBONYL DERIVATIVE; ESTER DERIVATIVE; LACTAM DERIVATIVE; NAPHTHYL GROUP; TITANIUM DERIVATIVE;

ARTICLE; CATALYSIS; CATALYST; CHEMICAL STRUCTURE; COMPLEX FORMATION; DERIVATIZATION; DIASTEREOISOMER; ENANTIOSELECTIVITY; FLUORINATION; HALOGENATION; ISOMER; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PRIORITY JOURNAL; REACTION ANALYSIS; STEREOCHEMISTRY; STRUCTURE ANALYSIS; X RAY CRYSTALLOGRAPHY;

EID: 33744988187     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.12.071     Document Type: Article

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