The highly stereoselective tandem Pummerer reaction/alpha-hydroxy imine rearrangement of E.P. alpha-fluoroalkyl-beta-sulfinylenamines affording chiral non-racemic fluoropyruvaldehydes N,S-ketals is described.
Highly stereoselective tandem Pummerer reaction alpha-hydroxy imine rearrangement of EP beta-sulfinylenamines
CRUCIANELLI, MARCELLO;
1997-01-01
Abstract
The highly stereoselective tandem Pummerer reaction/alpha-hydroxy imine rearrangement of E.P. alpha-fluoroalkyl-beta-sulfinylenamines affording chiral non-racemic fluoropyruvaldehydes N,S-ketals is described.File in questo prodotto:
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