Abstract
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The synthesis of (+)-(S)-(E)-γ-hydroxy-α,β-enoates 4 in moderate enantiomeric purities (36-54%) from the reaction of the camphor-derived α-sulfinyl acetate ester 3 with aldehydes is described.
The synthesis of (+)-(S)-(E)-γ-hydroxy-α,β-enoates 4 in moderate enantiomeric purities (36-54%) from the reaction of the camphor-derived α-sulfinyl acetate ester 3 with aldehydes is described.
The synthesis of (+)-(S)-(E)-γ-hydroxy-α,β-enoates 4 in moderate enantiomeric purities (36-54%) from the reaction of the camphor-derived α-sulfinyl acetate ester 3 with aldehydes is described.