Tetrahedron Letters p. 363 - 366 (1993)
Update date:2022-07-30
Topics: Reduction Diastereoselective Epoxides Functionalised Cyclic β-Ketosulphoxides
Armer, Richard
Simpkins, Nigel S.
A thiane oxide system 1, bearing a protected hydroxyl group, undergoes stereoselective acylation to give a range of β-ketosulphoxides 2a-e, which can then be reduced stereoselectively to give either of the corresponding hydroxysulphoxides 3 and 4.Further
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