Chemo-, regio- and stereoselective 1,3-dipolar cycloaddition of C-aryl-N-phenylnitrones over 3,5-bis(arylidene)-1-methylpiperidin-4-ones: synthesis of highly substituted novel spiro-isoxazolidines

Tetrahedron

Volumn 62, Issue 52, 2006, Pages 12380-12391

  Kumar, Raju Ranjith ^a   Perumal, Subbu ^a   Kagan, Henri B ^b   Guillot, Regis ^b  

^a MADURAI KAMARAJ UNIVERSITY   (India)

^b UNIVERSITÉ PARIS SUD   (France)

Author keywords

1,3 Dipolar cycloaddition; Nitrones; Piperidone; Spiro isoxazolidines; Transannular interaction

Indexed keywords

BENZYL DERIVATIVE; CARBON; ISOXAZOLIDINE DERIVATIVE; NITROGEN; NITRONE DERIVATIVE; OXYGEN; PIPERIDONE DERIVATIVE; SPIRO COMPOUND;

ARTICLE; CHEMICAL BOND; CHEMICAL REACTION; CYCLOADDITION; DIASTEREOISOMER; MOLECULAR INTERACTION; PRIORITY JOURNAL; STEREOCHEMISTRY; SYNTHESIS;

EID: 33750964906     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2006.09.106     Document Type: Article

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20. 1H NMR signal intensities.
21. For these compounds existing as mixture, identification of all signals of the aromatic carbons proved difficult.
22. The elemental analysis not done as they occur as mixture of compounds with different molecular formula.