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Volumn , Issue 9, 2000, Pages 1387-1398

Furo[3,4-b]benzofurans: Synthesis and reactions

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYLIC ACIDS; DERIVATIVES; SYNTHESIS (CHEMICAL);

EID: 0034616461     PISSN: 14704358     EISSN: None     Source Type: Journal    
DOI: 10.1039/b000619j     Document Type: Article
Times cited : (11)

References (90)
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    • (1984) Comprehensive Heterocydic Chemistry , vol.4 , pp. 657
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    • J. B. Hendrickson and W. A. Wolf, J. Org. Chem., 1968, 33, 3610. This reagent is especially suitable for diazo group transfer reactions, as the 4-sulfamoylbenzoic acid can be separated quite easily from the reaction mixture.
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    • 13C NMR structure 8 is preferred (see Experimental section).
    • 13C NMR structure 8 is preferred (see Experimental section).
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    • The literature of intramolecular Diels-Alder reactions is extensive. For reviews and examples see ref. 21. 21 (a) W. Oppolzer, Angew. Chem., 1977,89, 10;
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    • note
    • 24 for 11a reveal that the total charge density at Cb is lower than at Ca), but can be explained when the corresponding intermediates are taken into consideration (see Computational results).
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    • For an unregioselective ring opening reaction of homophthalic anhydride see: W. V. Murray and S. K. Hadden, J. Chem. Res., 1991, 279.
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    • 30
    • 30
  • 88
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    • note
    • -1 as a result of a B3LYP/6-31G*//B3LYP/6-31G* treatment (Table 2)).


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