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Hetero Diels-Alder reaction using nitroso dienophiles

Efficient hetero Diels-Alder reactions have been carried out using a-chloronitroso saccharides as dienophiles and various symmetrical and unsymmetrical dienes. Thus, 2,3 5,6-di-0-isopropyli-dene-l-C-nitroso-a-D-mannofuranosyl chloride 122, easily prepared from hydroximolactone 121 and tert-butyIhypochlorite, was proven to be a stable and highly reactive dienophilic compound [92]. [Pg.462]


See other pages where Hetero Diels-Alder reaction using nitroso dienophiles is mentioned: [Pg.269]    [Pg.144]    [Pg.144]    [Pg.283]    [Pg.361]    [Pg.452]    [Pg.452]    [Pg.452]    [Pg.231]    [Pg.1217]    [Pg.172]   
See also in sourсe #XX -- [ Pg.378 ]

See also in sourсe #XX -- [ Pg.378 ]




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Diels hetero

Diels-Alder Dienophile

Diels-Alder dienophiles

Diels-Alder reaction hetero-dienophiles

Diels-Alder reactions nitroso dienophiles

Dienophil

Dienophile

Dienophiles

Hetero-Diels-Alder

Hetero-Diels-Alder reaction

Hetero-dienophiles

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