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Internally neutral strategy

By introduction of an oxidizing directing group, Li and Wang demonstrated a regioselective ruthenium(ll)-catalyzed isoquinolone synthesis through oxidative cyclization of JV-methoxybenzamides with internal alkynes (Eq. (7.24)) [31]. This redox-neutral strategy circumvents the use of wasteful metal oxidants, and the reaction could take place at much milder conditions with broad substrate scope. [Pg.206]

Hand, B.M., Treagust, D.F. Application of a conceptual conflict strategy to enhance student learning of acids and bases. Research in Science Education 18 (1988), 53 Hawkes, S.J. Arrhenius confuses students. Journal of Chemical Education 69 (1992), 542 Ross, B., Munby, H. Concept mapping and misconceptions A study of high school students understandings of acids and bases. International Journal of Science Education 13 (1991), 11 Schmidt, H.-J. A label as a hidden persuader Chemists neutralization concept. International Journal of Science Education 13 (1991), 459... [Pg.204]

See other pages where Internally neutral strategy is mentioned: [Pg.104]    [Pg.92]    [Pg.134]    [Pg.113]    [Pg.44]    [Pg.33]    [Pg.409]    [Pg.112]    [Pg.172]    [Pg.10]    [Pg.621]    [Pg.433]    [Pg.433]    [Pg.268]    [Pg.483]    [Pg.141]    [Pg.632]    [Pg.401]    [Pg.357]    [Pg.5]    [Pg.299]    [Pg.357]    [Pg.2]    [Pg.28]    [Pg.27]   
See also in sourсe #XX -- [ Pg.52 ]



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Internal neutralization

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