HALOGEN AS A READILY CLEAVABLE PROTECTIVE GROUP FOR REACTIVE POSITIONS IN PHENOLS AND PHENOLIC COMPOUNDS
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00304947609355637
Reference8 articles.
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3. Das kondensationsverhalten bromierter phenole, der aufbau linearer und bromierter phenolischer mehrkernverbindungen
4. Darstellung und spektroskopische analyse von oligo{[4-(1,1,3,3-tetramethylbutyl) (bzw. 4-octyl)-2-hydroxy-1,3-phenylen]methylen}en und ihrer Ausgangsverbindungen
5. Kämmerer, H. and Happel, G. Unpublished results
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1. Synthesis and Characterization of Structurally Uniform Model Oligomers of Polybenzoxazine;Macromolecules;1998-03-26
2. 1,3-Diphenylpropane-1,3-diamines, III: Synthesis of 1,3-Bis(hydroxy-halogenophenyl)-propane-1,3-diamines and their Pt(II) ComplexesPart A: Synthesis of the Ligands;Archiv der Pharmazie;1994
3. Annelated calix[4]arenes, a new type of oligomeric calixarenes;Tetrahedron Letters;1992-02
4. The photochemistry of indomethacin;Journal of Photochemistry and Photobiology A: Chemistry;1991-09
5. Synthesis and structural characterization of regio-controlled oligomers from 2-naphthalensulfonic acid and formaldehyde;Tetrahedron;1990-01
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