Synthesis of toxyloxanthone B

Tetrahedron

Volumn 70, Issue 6, 2014, Pages 1283-1288

  Giallombardo, Daniele ^a,b   Nevin, Adam C ^a   Lewis, William ^a   Nawrat, Christopher C ^a   Kitson, Russell R A ^a   Moody, Christopher J ^a  

^a UNIVERSITY OF NOTTINGHAM   (United Kingdom)

^b UNIVERSITY OF PALERMO   (Italy)

Author keywords

Benzyne addition; Claisen rearrangement; Natural products; Oxygen heterocycle; Xanthones

Indexed keywords

1,3,6 TRIBENZYLOXY 7 METHOXYMETHOXY 9H XANTHEN 9 ONE; 3,6 DIBENZYLOXY 1,7 DIHYDROXY 9H XANTHEN 9 ONE; 5,9,11 TRIBENZYLOXY 3,3 DIMETHYLPYRANO[3,2 A]XANTHEN 12(3H) ONE; 5,9,11 TRIBENZYLOXY 3,3 DIMETHYLPYRANO[3,2 A]XANTHEN 12(3H) ONE (TOXYLOXANTHONE B TRIMETHYL ETHER); 5,9,11 TRIBENZYLOXY 3,3 DIMETHYLPYRANO[3,2 A]XANTHEN 12(3H) ONE (TOXYLOXANTHONE B); 7 (2,2 DIMETHYLBUT 3 YNYL) 1,3,6 TRIBENZYLOXY 9H XANTHEN 9 ONE; 7 HYDROXY 1,3,6 TRIBENZYLOXY 9H XANTHEN 9 ONE; ANION; HYDROXYL GROUP; SALICYLIC ACID METHYL ESTER; TOXYLOXANTHONE B; TRIFLUOROACETIC ANHYDRIDE; UNCLASSIFIED DRUG; XANTHONE DERIVATIVE;

ARTICLE; CHROMATOGRAPHY; CYCLIZATION; DRUG SYNTHESIS; ELECTROSPRAY; INFRARED SPECTROSCOPY; MACLURA POMIFERA; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; NUCLEOPHILICITY; PRIORITY JOURNAL; PROTON TRANSPORT; X RAY CRYSTALLOGRAPHY;

EID: 84892798720     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2013.12.055     Document Type: Article

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