New rhenium(III) semiclathrochelates with biorelevant apical substituents: Synthesis, X-ray structure and reactivity
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文摘

Tris-dioximate rhenium(III) semiclathrochelates underwent reduction domino-reactions.

These ligand-centered reactions gave the reduced diimine-iminoximate derivatives.

Template condensation on Re3 + ion afforded its formylphenylboron-capped tris-dioximate.

This semiclathrochelate undergoes a further H+-catalyzed condensation with isoniazid.

The obtained semiclathrochelate hydrazone contains an apical vector substituent.

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