Diastereoselective access to polyoxygenated polycyclic spirolactones through a rhodium-catalyzed [3+2] cycloaddition reaction: Experimental and theoretical studies

Chemistry - A European Journal

Volumn 19, Issue 7, 2013, Pages 2467-2477

  Rodier, Fabien ^a   Rajzmann, Michel ^a   Parrain, Jean Luc ^a   Chouraqui, Gaëlle ^a   Commeiras, Laurent ^a  

^a AIX MARSEILLE UNIVERSITÉ   (France)

Author keywords

azo compound; cycloaddition; density functional calculations; spiro compounds; ylides

Indexed keywords

1 ,3-DIPOLARCYCLOADDITION; AZO COMPOUND; BIOSYNTHETIC PATHWAY; COMPUTATIONAL STUDIES; CYCLOADDITION REACTION; DIASTEREOSELECTIVE; FUNCTIONALIZED; LACTONE MOIETY; POLYCYCLIC SYSTEMS; RHODIUM-CATALYZED; SCHISANDRA; SPIRO COMPOUNDS; STEREOCENTERS; SYNTHETIC UTILITY; THEORETICAL STUDY; THEORETICAL TREATMENTS; TOTAL SYNTHESIS; YLIDES;

CATALYSIS; CYCLOADDITION; DENSITY FUNCTIONAL THEORY; ESTERS; RHODIUM; STEREOSELECTIVITY;

RHODIUM COMPOUNDS;

LACTONE; LIGAND; POLYCYCLIC HYDROCARBON; RHODIUM; SPIRO COMPOUND;

ARTICLE; CHEMICAL STRUCTURE; CHEMISTRY; CYCLOADDITION; STEREOISOMERISM; THEORETICAL MODEL;

CYCLOADDITION REACTION; LACTONES; LIGANDS; MODELS, THEORETICAL; MOLECULAR STRUCTURE; POLYCYCLIC COMPOUNDS; RHODIUM; SPIRO COMPOUNDS; STEREOISOMERISM;

EID: 84873375029     PISSN: 09476539     EISSN: 15213765     Source Type: Journal    
DOI: 10.1002/chem.201203155     Document Type: Article

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