Stereoselective synthesis of new classes of atropisomeric compounds through a tandem Michael reaction-azacyclization process. Part 2

Tetrahedron Asymmetry

Volumn 15, Issue 1, 2004, Pages 139-145

  Le Gac, Stéphane ^a   Monnier Benoit, Nicolas ^a   Metoul, Lionel Doumampouom ^a   Petit, Samuel ^b   Jabin, Ivan ^a  

^a UNIVERSITÉ DU HAVRE   (France)

^b UNIVERSITÉ DE ROUEN   (France)

Author keywords

[No Author keywords available]

Indexed keywords

IMINE; KETONE DERIVATIVE; PYRROLE DERIVATIVE;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; CHIRALITY; CYCLIZATION; MICHAEL ADDITION; PRIORITY JOURNAL; REACTION ANALYSIS; ROTATION; STEREOCHEMISTRY; STRUCTURE ANALYSIS; SYNTHESIS;

EID: 0347418208     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetasy.2003.10.025     Document Type: Article

References (18)

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15. In both cases (i.e., under heating conditions or with a Lewis acid catalysis), the obtained major diastereomer was identical.
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