Regioselective monoalkylations of the vicinal cis-diol group in mannopyranosides using diaryldiazoalkanes-tin(II) chloride
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
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1. Tuneable regioselectivity during the mono-etherification of the 2,3-diol of a mannose derivative;Carbohydrate Research;2014-03
2. Diarylmethyl Ethers for the Protection of Polyols;Journal of Chemistry;2013
3. Monoallylation of 1,2-Diols by Pd/Sn Bimetallic Catalysis;Chemistry - A European Journal;2012-01-27
4. Mono-etherification of racemic propane-1,2-diol by a tin(II) bromide catalyzed reaction with diazofluorene and a study of the Pseudomonas cepacia lipase catalyzed acetylation of the mono-ethers;Tetrahedron: Asymmetry;2012-01
5. Resolution of a racemic 1,2-diol using triphenylmethyl protection of the primary hydroxyl group and Mucor miehei lipase (Lipozyme) for the kinetic resolution;Tetrahedron: Asymmetry;2011-10
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