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The synthesis of some novel stilbene dimers incorporating diamide tethers: studies in single electron transfer oxidation (FeCl3).


ABSTRACT: The FeCl3 oxidative cascade reaction of the acetamido stilbene 1 which we reported some years ago produced the first atropodiastereomeric indolostilbene hybrid 3. By contrast, recent investigation of the oxidation of the stilbene succinamide dimer 72 (FeCl3/CH2Cl2) appears, on the basis of spectroscopic evidence, to have produced the bridged macrocyclic indoline 73.

SUBMITTER: Alehashem MS 

PROVIDER: S-EPMC9077395 | biostudies-literature | 2018 Jan

REPOSITORIES: biostudies-literature

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The synthesis of some novel stilbene dimers incorporating diamide tethers: studies in single electron transfer oxidation (FeCl<sub>3</sub>).

Alehashem Maryam Sadat MS   Ariffin Azhar A   Qatran Al-Khdhairawi Amjad Ayad AA   Thomas Noel F NF  

RSC advances 20180111 5


The FeCl<sub>3</sub> oxidative cascade reaction of the acetamido stilbene 1 which we reported some years ago produced the first atropodiastereomeric indolostilbene hybrid 3. By contrast, recent investigation of the oxidation of the stilbene succinamide dimer 72 (FeCl<sub>3</sub>/CH<sub>2</sub>Cl<sub>2</sub>) appears, on the basis of spectroscopic evidence, to have produced the bridged macrocyclic indoline 73. ...[more]

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