Maleimide cycloadditions by sulfinyldienes: Is the sulfur configuration the only controller of the diastereofacial selectivity?

Tetrahedron

Volumn 61, Issue 32, 2005, Pages 7719-7726

  Aversa, Maria C ^a   Barattucci, Anna ^a   Bonaccorsi, Paola ^a   Faggi, Cristina ^b   Gacs Baitz, Eszter ^c   Marrocchi, Assunta ^d   Minuti, Lucio ^d   Taticchi, Aldo ^d  

^a UNIVERSITY OF MESSINA   (Italy)

^b UNIVERSITY OF FLORENCE   (Italy)

^c INSTITUTE OF EXPERIMENTAL MEDICINE   (Hungary)

^d UNIVERSITY OF PERUGIA   (Italy)

Author keywords

Cyclohexylsulfinyl dienes; Diastereofacial selectivity; Diels Alder cycloadditions; N Phenylmaleimide

Indexed keywords

ALKADIENE; CYCLOHEXANE DERIVATIVE; CYCLOHEXENE DERIVATIVE; MALEIMIDE; SULFENIC ACID DERIVATIVE; SULFUR; THIOL DERIVATIVE;

ARTICLE; CHEMICAL PROCEDURES; CHEMICAL REACTION; CYCLOADDITION; PRESSURE; PRIORITY JOURNAL; REACTION ANALYSIS;

BETULACEAE;

EID: 21844475102     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.05.089     Document Type: Article

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