Stereoselective synthesis of substituted γ-butyrolactones from γ-hydroxy-α,β-unsaturated phenyl sulfones
- 1 January 1993
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 49 (43) , 9787-9800
- https://doi.org/10.1016/s0040-4020(01)80181-2
Abstract
No abstract availableThis publication has 32 references indexed in Scilit:
- Nitro alkanes in organic synthesis: An efficient stereoselective synthesis of (+)-trans whisky lactone and (+)-eldanolide from nitro alkane synthons and using bakers' yeast reduction as the key stepTetrahedron, 1993
- A novel stereoselective synthesis of substituted γ-butyrolactonesTetrahedron Letters, 1992
- A convenient synthesis of .gamma.-hydroxy .alpha.,.beta.-unsaturated sulfonesThe Journal of Organic Chemistry, 1991
- A practical route to (E)-γ-hydroxy-αβ-unsaturated phenyl sulfonesTetrahedron, 1990
- Enantioselective synthesis of hydroxy α-amino acids. (-)-- and (-) --γ-hydroxynorvalinesTetrahedron, 1990
- Facile synthesis of E-γ-hydroxy-α,β-unsaturated sulfones from aldehydesTetrahedron Letters, 1990
- Conformational Analyses of Stegobinone and 1'-Epi-stegobinoneHETEROCYCLES, 1990
- New general asymmetric synthesis of versatile .gamma.-alkylated butenolides and its application to expeditious synthesis of the chiral Geissman-Waiss lactones useful for (+)-retronecine synthesisThe Journal of Organic Chemistry, 1989
- Stereoselective reactions. 14. Efficient enantioselective construction of quaternary carbon centers by the sequential dialkylation of (S)-.gamma.-[(trityloxy)methyl]-.gamma.-butyrolactone. Synthesis of optically active .beta.,.beta.-disubstituted .gamma.-butyrolactonesThe Journal of Organic Chemistry, 1988
- A tactically novel alternative to acyclic stereoselection based on the concept of a replicating chiron - 1,5-C-methyl substitutionTetrahedron Letters, 1985