4-O-TfO-2,3-anhydro-β-L-ribopyranosides as chiron: A formal synthesis of canadensolide
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Total Synthesis of (−)-Dihydrosporothriolide Utilizing an Indium-Mediated Reformatsky–Claisen Rearrangement;The Journal of Organic Chemistry;2014-06-11
2. ChemInform Abstract: 4-O-Tf-2,3-Anhydro-β-L-ribopyranosides as Chiron: A Formal Synthesis of Canadensolide.;ChemInform;2010-08-04
3. Synthesis of β,γ-disubstituted-γ-lactones through a Johnson–Claisen rearrangement: a short route to xylobovide, nor-canadensolide, canadensolide, sporothriolide and santolinolide;Tetrahedron: Asymmetry;2009-12
4. Chiral vicinal diols as platforms for separable diastereomers in Johnson–Claisen rearrangement: a new short route to (−)-nor-canadensolide, (−)-canadensolide and (−)-sporothriolide;Tetrahedron Letters;2009-03
5. Addition/Oxidative Rearrangement of 3-Furfurals and 3-Furyl Imines: New Approaches to Substituted Furans and Pyrroles;Journal of the American Chemical Society;2008-03-01
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