ORTHOESTER CLAISEN REARRANGEMENT OF AD-GLUCOSE-DERIVED SPIROCYCLIC SUBSTRATE
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry,Biochemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/10256018808623883
Reference14 articles.
1. Claisen Rearrangements
2. The thermal, aliphatic Claisen rearrangement
3. The Claisen Rearrangement in Organic Synthesis; 1967 to January 1977
4. Ortho ester Claisen rearrangements of three 3-C-(hydroxymethyl)methylene derivatives of hexofuranose: stereoselective introduction of a quaternary center on C-3 of D-ribo-, L-lyxo-, and D-arabino-hexofuranoses
5. Claisen rearrangement of (Z)-3-deoxy-3-C-[(hydroxymethyl)methylene]-1,2:5,6-di-O-isopropylidene-.alpha.-D-ribo-hexofuranose with triethyl orthopropionate
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1. Applications of alkyl orthoesters as valuable substrates in organic transformations, focusing on reaction media;RSC Advances;2020
2. Enantioselective Total Synthesis of (+)-Neostenine;Chemistry - A European Journal;2016-02-02
3. ChemInform Abstract: Orthoester Claisen Rearrangement of a D-Glucose-Derived Spirocyclic Substrate.;ChemInform;2010-05-25
4. One or More CH, CC, and/or CC Bond(s) Formed by Rearrangement;Comprehensive Organic Functional Group Transformations II;2005
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