Tetrahedron Letters p. 4389 - 4392 (1993)
Update date:2022-09-26
Topics:
Paterson, Ian
Tillyer, Richard D.
Ryan, Glen R.
The β-hydroxyketones 7, 20 and 22 were prepared by stereocontrolled aldol reactions of (S)- and (R)-18 with the enal 8.Acetonide hydrolysis gave the bicyclic acetals 23-25, while the benzoate 26 gave the tetrahydropyran 6, corresponding to an A-ring subun
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Doi:10.1016/j.tet.2018.05.016
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