Asymmetric Synthesis of Spiro-epoxyoxindoles by the Catalytic Darzens Reaction of Isatins with Phenacyl Bromides
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https://figshare.com/articles/dataset/Asymmetric_Synthesis_of_Spiro_epoxyoxindoles_by_the_Catalytic_Darzens_Reaction_of_Isatins_with_Phenacyl_Bromides/2264326
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资源简介:
The asymmetric Darzens reaction between
phenacyl bromides and N-protected isatins was developed
to synthesize potentially bioactive spiro-epoxyoxindoles. The
optically active products were obtained in moderate to good yields
and enantioselectivities catalyzed by chiral N,N′-dioxide-Co(acac)2 complexes.
A retro-aldol process accompanying the ring-closure step was observed
in the process. A chiral control step was determined to be the initial
aldol addition.
创建时间:
2016-02-17



