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Furo 3,4-<7 oxazole, Diels-Alder reactions

Reck and Friedrichsen reported a synthesis of furo[3,4-, oxazole 218 from diazo derivative 217. Furoxazole 218 can undergo Diels-Alder reaction with dienophiles such as naphthoquinone 219 to give, in this case, the adduct 220 in a modest yield (Scheme 65) <1998JOC7680>. [Pg.523]

See other pages where Furo 3,4-<7 oxazole, Diels-Alder reactions is mentioned: [Pg.20] [Pg.67] [Pg.70] [Pg.42] [Pg.23]

See also in sourсe #XX -- [ Pg.20 , Pg.81 ]

See also in sourсe #XX -- [ Pg.20 , Pg.81 ]

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Furo oxazoles

Oxazole Diels-Alder reactions

Oxazole reactions

Oxazoles reactions

Oxazoles, Diels-Alder reaction