Bioorganic and Medicinal Chemistry Letters p. 199 - 202 (1997)
Update date:2022-08-11
Topics:
Iriye, Ryozo
Takai, Katsuki
Noguchi, Masakazu
(R)-1-(2-oxocyclopentyliden)-2-alkanols (1r-a and 1r-b) and the (S)-forms, 1s-a and 1s-b, were enantiomerically synthesized from (R)-2-[(R)-O-MEMmandelyloxy]alkanals (6r-a and 6r-b) and the (S)-alkanals, 6s-a and 6s-b. The (R)-isomers (1r-a and 1r-b) showed bio-antimutagenic acitivity against UV-induced Eschericia coli WP2 B/r Trp-.
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