Diastereomerically Pure 1,2-Diols by Nucleophilic Displacement Reactions of 3-Oxetanols – A Study Directed Towards the Identification of Suitable Nucleophiles and the Elucidation of Possible Side Reactions
Author:
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/(SICI)1099-0690(199810)1998:10%3C2161::AID-EJOC2161%3E3.0.CO;2-L/fullpdf
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1. The Paternò-Büchi Reaction of 3-Heteroatom-Substituted Alkenes as A Stereoselective Entry to Polyfunctional Cyclic and Acyclic Molecules
2. 3-Trimethylsilyloxy-oxetanes via a highly selective paterno-büchi reaction
3. Diastereomerically Pure 3‐(Silyloxy)oxetanes by a Selective Paternò‐Büchi Reaction
4. Stereoselective photocycloaddition of silyl enol ethers to aldehydes. Configurational control of three stereogenic centers in oxetanes
5. Silyl enol ethers in Paternò-Büchi reactions. Functional group tolerance and the effect of β-alkyl substitution
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1. Stereoselective and Regioselective Pinacol-Type Rearrangement of a Fused Bicyclic Oxetanol Scaffold;European Journal of Organic Chemistry;2017-10-18
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3. Stereoselective synthesis of 2,3,4-highly substituted oxetanes by intramolecular C–C bond forming Michael addition;Chemical Communications;2016
4. Facile Perhydrolysis of Oxetanes Catalyzed by Molybdenum Species;Organic Letters;2014-10-15
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