Stereoselective synthesis of 1,3-disaccharides through diels-alder reactions: Part 2[ ]: Convenient protecting groups for heterodienes and conformational evaluations

Journal of Carbohydrate Chemistry

Volumn 28, Issue 3, 2009, Pages 124-141

  Gabrielli, Gabriele ^a   Melani, Fabrizio ^a   Bernasconi, Sara ^a   Lunghi, Carlotta ^a   Richichi, Barbara ^a   Rollin, Patrick ^b   Venturi, Chiara ^a   Nativi, Cristina ^a  

^a UNIVERSITY OF FLORENCE   (Italy)

^b Université d'Orléans   (France)

Author keywords

Conformational studies; Diels alder; Disaccharides; Stereoselective synthesis

Indexed keywords

ALNUS;

EID: 68149137675     PISSN: 07328303     EISSN: 15322327     Source Type: Journal    
DOI: 10.1080/07328300902752223     Document Type: Article

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23. As most Diels-Alder reactions involving nonsymmetrical cycloaddents, these cycloadditions are nonsynchronous. The model of diradicaloids for the transition states of these reactions might contribute for the differential electronic factors intervening in reported cycloadditions.