19719-96-1Relevant articles and documents
Conversion of γ-substituted bicyclo[2.2.1] (Z)-vinylsulfones to the corresponding (E)-allylsulfones
Cossu, Sergio,Peluso, Paola,Moretto, Flavio,Marchetti, Mauro
, p. 2253 - 2256 (2007/10/03)
The preparation of bicyclo[2.2.1] (E)-allylsulfones starting from the corresponding (Z)-vinylsulfones is described. Starting from 2,3- bis(phenylsulfonyl)norbornadiene 1, the Michael addition of organometallic reagents followed by the base catalyzed isome
1,3-Bis(phenylsulfonyl)allene as a new reagent for cycloaddition methodology
Bull, James R.,Desmond-Smith, Nicholas S.,Heggie, Steven J.,Hunter, Roger,Tien, Feng-Chang
, p. 900 - 902 (2007/10/03)
1,3-Bis(phenylsulfonyl)allene 2 has been synthesised as a new reagent for cycloaddition methodology. In contrast to phenylsulfonylallene 1, thermal reaction of 2 with substituted 1,3-dienes gave both [2+2] as well as [2+4] cycloaddition products.
Stereochemistry of Diels-Alder Reactions of Allenic Sulphones; Transfer of Assymetry from Allenic to Norbornene Systems
Barbarella, Giovanna,Cinquini, Mauro,Colonna, Stefano
, p. 1646 - 1649 (2007/10/02)
Diels-Alder reactions of chiral allenic sulphones afford as main products the diastereomers derived by attack of the diene from the less hindered side of the double bond α to the sulphonyl group; starting from menthyl sulphinate, asymmetry is transmitted