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Iron-Catalyzed Reactions in Organic Synthesis

✍ Scribed by Carsten Bolm; Julien Legros; Jacques Le Paih; Lorenzo Zani


Publisher
John Wiley and Sons
Year
2005
Weight
8 KB
Volume
36
Category
Article
ISSN
0931-7597

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πŸ“œ SIMILAR VOLUMES


Iron-Catalyzed Aziridination Reactions
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## Abstract A small quantity of iron(II) triflate (2.5 to 5 mol%) catalyzes the aziridination reactions of enol silyl ethers with tosylimino(iodo)benzene (PhINTs) in acetonitrile to give α‐__N__‐tosylamido ketones by subsequent aziridine ring opening. Olefins are converted into aziridines by 5 mol%

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Iron-catalyzed hydrosilylation reactions
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## Abstract Iron‐catalyzed hydrosilylation is one of the most popular reduction reactions owing to the high natural abundance, low cost and low toxicity of iron and silicon. This paper introduces an advance in iron‐catalyzed hydrosilylation of olefins, aldehydes, ketones and amides. Some reactions

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