Showing papers on "Ferrier carbocyclization published in 2013"
TL;DR: A review of recent developments in the use of promoters for the Ferrier rearrangement of O-, N-, C- and S-nucleophiles with glycals can be found in this paper.
121 citations
TL;DR: In this paper, the combination of α-zirconium sulfophenylphosphonate-methanphosphoneate and lithium bromide change the regioselectivity of this process affording 2-deoxy sugars in good yields.
Abstract: Layered α-zirconium sulfophenylphosphonate-methanphosphonate is a solid acid catalyst that catalyzes Ferrier rearrangement from d-glycals and alcoholic nucleophiles under mild reaction conditions in short time and good yields. Notably, the combination of α-zirconium sulfophenylphosphonate-methanphosphonate and lithium bromide change the regioselectivity of this process affording 2-deoxy sugars in good yields.
16 citations
TL;DR: The Ferrier rearrangement is performed with glucal (I) and a variety of structurally different alcohols as mentioned in this paper, and it is performed in the Ferrier re-arrangement.
Abstract: The Ferrier rearrangement is performed with glucal (I) and a variety of structurally different alcohols.