Abstract:An efficient iron-catalyzed hydroarylation of 1,3-dienes with indoles has been developed for the first time. This protocol is the use of green and inexpensive earth-abundant metal iron as the catalyst....
The azidocyanation and diazidation were carried out on 1,3-dienes compounds, using TMSN3 as the azide source and MeCN as the cyanoalkylation reagent. This method exhibits excellent functional group tolerance, a...
The azidocyanation and diazidation were carried out on 1,3-dienes compounds, using TMSN3 as the azide source and MeCN as the cyanoalkylation reagent. This method exhibits excellent functional group tolerance, a...
A Fe(OTf)3 and γ-cyclodextrin catalyzed hydroarylation of alkenes with 1-naphthols and 2-naphthols is demonstrated. This efficient and general method could deliver a wide range of benzyl-naphthols from readily available starting materials with high chemo- and regioselectivity in up to 99% yield with no need for a strong base or additive.
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