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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 41, 2011 - Issue 9
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Original Articles

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

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Pages 1348-1356 | Received 29 Sep 2009, Published online: 30 Mar 2011

REFERENCES

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  • Giles , R. G. F. ; Gruchlik , Y. 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 . Arkivoc 2004 , 134 – 151 .
  • Green , I. R. ; Giles , R. G. F. ; Gruchlik , Y. An investigation into steric factors in the stereoselective formation of naphthopyrans from 4-naphthyldioxolanes . S. Afr. J. Chem. 1997 , 50 ( 2 ), 75 – 81 .
  • Green , I. R. ; Hugo , V. I. ; Mei , M. N. Bromination products of 2-substituted 5,7-dimethoxy-4-naphthols . Synth. Commun. 2006 , 36 , 331 – 346 .
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  • Giles , R. G. F. ; Rickards , R. W. ; Senanayake , B. S. Stereoselective isomerisations of 4-(3′,5′-dimethoxyphenyl)-2,5-dimethyl-1,3-dioxolanes: Temperature-dependent formation of either isochromanes or dihydroisobenzofurans . J. Chem. Soc. Perkin Trans. 1 1996 , 2241 .
  • Aggarwal , A. ; Giles , R. G. F. ; Green , I. R. ; Oosthuizen , F. J. ; Taylor , C. P. Synthesis in enantiopure form of four diasterioisomeric naphthopyranquinones derived from aphid insect pigments . Org. Biomol. Chem. 2005 , 3 , 263 – 273 .

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