
Bulletin of the Chemical Society of Japan p. 180 - 184 (1989)
Update date:2022-09-26
Kanemasa, Shuji
Nakagawa, Norihiko
Suga, Hiroyuki
Tsuge, Otohiko
Under acid catalysis, α-hydroxy-γ-oxo acetals which are readily available from the nitrile oxide cycloaddition route are smoothly convrted into γ-oxo esters.This unusual and high-yield transformation involves rare acid-catalyzed deconjugation of the inter
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Doi:10.1021/jm100095x
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(1989)Doi:10.1021/ol1006295
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