Novel formal [2+3] cycloaddition between substituted phenols and furan

Tetrahedron Letters

Volumn 48, Issue 46, 2007, Pages 8238-8241

  Bérard, Didier ^a   Jean, Alexandre ^a   Canesi, Sylvain ^a  

^a UNIVERSITÉ DU QUÉBEC À MONTRÉAL   (Canada)

Author keywords

Cycloaddition 2+3 ; Furan; Hypervalent iodine; Phenols

Indexed keywords

FURAN; IODOBENZENE DIACETATE; PHENOL DERIVATIVE; TRIFLUOROETHANOL; UNCLASSIFIED DRUG;

ARTICLE; CYCLOADDITION; OXIDATION; QUANTUM YIELD; REACTION ANALYSIS; SUBSTITUTION REACTION;

EID: 35348829739     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.09.062     Document Type: Article

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42. 3 and 3 mL of brine. The solution is concentrated under vacuum and the residue is purified by silica gel chromatography with an appropriate mixture of ethyl acetate/hexane.
43. 3) δ = 160.1, 151.2, 136.5, 131.8, 131.4, 124.4, 110.5, 99.9, 88.9, 85.1, -0.8.
44. 3) δ = 150.5, 133.8, 129.7, 128.5, 125.0, 123.9, 100.5, 87.8, 85.3, 34.0, 29.1, 20.8.
45. 3) δ = 150.1, 143.3, 141.1, 131.1, 126.5, 122.8, 116.7, 115.7, 111.6, 106.3, 34.1, 31.4.