Model Route to 5-Bromo-3,4-dihydro-4-hydroxy-7,9,10-trimethoxy-1,3-dimethyl-1H-naphtho[2,3-c]pyran: A Potential Precursor to Extended Quinones
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/00397911.2010.482039
Reference9 articles.
1. The stereoselective formation of naphtho[1,2-c]pyrans, angular analogues of the aphin-derived glucoside B, by an intramolecular version of the Mukaiyama reaction of 4-naphthyldioxolanes
2. Syntheses of 2,5-dimethyl-4-naphth-2'-yldioxolanes and their stereoselective isomerization to naphtho[1,2-c]pyrans, angular analogues of glucoside B, a cleavage product of the aphid insect pigments the protoaphins
3. Bromination Products of 2‐Substituted 5,7‐Dimethoxy‐4‐Naphthols
4. Palladium-Assisted (Z)-(E) Isomerization of Styrenes
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1. ChemInform Abstract: Model Route to 5-Bromo-3,4-dihydro-4-hydroxy-7,9,10-trimethoxy-1,3-dimethyl-1H-naphtho[ 2,3-c]pyran: A Potential Precursor to Extended Quinones.;ChemInform;2011-09-19
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