Nucleophilic coupling of alkali 2-naphthoxides with 1-bromo-2 naphthols. Ion-pairing and halogen dance in the formation of 1,1′-binaphthalene-2,2′-diols
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1995/P2/P29950001853
Reference21 articles.
1. SYNTHETIC APPROACHES TO BINAPHTHALENES. A REVIEW
2. Modern methods of aryl-aryl bond formation
3. The Directed Synthesis of Biaryl Compounds: Modern Concepts and Strategies
4. The oxidative cross-coupling of substituted 2-naphthols, part I: The scope and limitations
5. Über β‐Binaphthol und β‐Oxy‐α,β‐naphthyläther
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1. ChemInform Abstract: Nucleophilic Coupling of Alkali 2-Naphthoxides with 1-Bromo-2- naphthols. Ion-Pairing and Halogen Dance in the Formation of 1,1′- Binaphthalene-2,2′-diols;ChemInform;2010-08-12
2. Some applications of zirconium(IV) tetrachloride (ZrCl4) and zirconium(IV) oxydichloride octahydrate (ZrOCl2.8H2O) as catalysts or reagents in organic synthesis;Journal of the Iranian Chemical Society;2008-06
3. Electrophilic Amination of 4-Fluorophenol with Diazenes: A Complete Removal of the Fluorine Atom;The Journal of Organic Chemistry;2004-02-24
4. Steric effects in the synthesis of ortho-substituted 1,1'-binaphthalene derivatives by the SRN1 and the Stille reaction;Arkivoc;2003-10-16
5. ZrCl4-promoted halogen migration during an electrophilic amination of halogenated phenolsElectronic supplementary information (ESI) available: spectroscopic data (1H NMR,13C NMR, IR, MS), mp and elemental analysis (or HRMS) for the products 3 and 4. See http://www.rsc.org/suppdata/cc/b2/b203622c/Dedicated to Professor Waldemar Adam, University of Würzburg, Germany, on the occasion of his 65th birthday.;Chemical Communications;2002-06-12
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