Stereoselective synthesis of hydroxypyrrolidines and hydroxypiperidines by cyclization of γ-oxygenated-α,β-unsaturated sulfones

[1]  J. Carretero,et al.  EFFICIENT STEREOSELECTIVE ACCESS TO POLYHYDROXYLATED INDOLIZIDINE COMPOUNDS BASED ON GAMMA -HYDROXY-ALPHA ,BETA -UNSATURATED SULFONES , 1995 .

[2]  M. Francis,et al.  The diastereofacial selectivity in the intramolecular 1,4-conjugate additions generating substituted tetrahydrothiopyrans follows the Cieplak model , 1995 .

[3]  J. Carretero,et al.  Stereoselective approach to optically pure syn 2-amino alcohol derivatives , 1994 .

[4]  K. Maeda,et al.  Stereoselective total syntheses of (−)-desoxoprosopinine and (−)-desoxoprosophylline : palladium(O)-catalyzed intramolecular N-alkylation for the key piperidine ring formation , 1994 .

[5]  M. Fujita,et al.  Highly stereoselective 6-exo ring-closure of 5-substituted hept-6-enyl radicals , 1993 .

[6]  M. Francis,et al.  Diastereofacial selectivity in intramolecular 1,4-conjugate additions: conclusive evidence for the importance of ground-state conformations and the .sigma.* orbital effect , 1993 .

[7]  P. Fuchs,et al.  Regiospecific silver[I] promoted, palladium[O]-catalyzed intramolecular addition of aryl iodides to vinyl sulfones. , 1993 .

[8]  N. Simpkins Sulphones in organic synthesis , 1993 .

[9]  Y. Nagao,et al.  Recent progress in asymmetric synthesis of pyrrolizidines , 1990 .

[10]  J. Carretero,et al.  A practical route to (E)-γ-hydroxy-αβ-unsaturated phenyl sulfones , 1990 .

[11]  M. Hirama,et al.  Conjugate addition of internal nucleophile to chiral vinyl sulfoxides with stereogenic center at the allylic carbon. “intramolecular” double asymmetric induction , 1988 .

[12]  D. Spellmeyer,et al.  Force-field model for intramolecular radical additions , 1987 .

[13]  P. Fuchs,et al.  Multiply convergent syntheses via conjugate-addition reactions to cycloalkenyl sulfones , 1986 .