Quinoline β-lactams by Rh(II)-catalyzed highly steroselective intramolecular carbene insertion into a carbon-hydrogen bond

Arkivoc

Volumn 2005, Issue 13, 2005, Pages 1-7

  Muroni, Daniele ^a   Saba, Antonio ^a  

^a UNIVERSITY OF SASSARI   (Italy)

Author keywords

lactam; C H insertion; Chemoselectivity; Diazoamide; Intramolecular cyclization; Metal carbene; Stereoselectivity

Indexed keywords

2 DIAZO 1 (3,4 DIHYDRO 2H QUINOLIN 1 YL) BUTANE 1,3 DIONE; 2 DIAZO 3 (3,4 DIHYDRO 2H QUINOLIN 1 YL) 3 OXOPROPIONIC ACID ETHYL ESTER; 2 DIAZO 3 (3,4 DIHYDRO 2H QUINOLIN 1 YL) 3 OXOPROPIONIC ACID MENTHYL ESTER; AMIDE; BETA LACTAM DERIVATIVE; CARBENE; CARBON; QUINOLINE DERIVATIVE; REAGENT; RHODIUM TETRAACETATE; SULFADIAZINE; UNCLASSIFIED DRUG;

ARTICLE; CATALYSIS; CATALYST; CHEMOSENSITIVITY; CHIRALITY; DECOMPOSITION; HYDROGEN BOND; MOLECULAR DYNAMICS; MOLECULAR INTERACTION; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 15544377984     PISSN: 14246376     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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