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Aldol-like intramolecular cyclization

Aldol Reactions.— Baldwin has extended the nomenclature for classifying ring-closures to include intramolecular aldol reactions. Observations of the modes of cyclization of polyketonic substrates have shown that, for example, 6-(enolendo)-exo-trig cyclizations are indeed favoured whereas the five-membered version is disfavoured (Scheme 50). Such generalizations may prove powerful aids to recognition of likely pathways that cyclizations may follow when a multitude of cyclization modes are formally possible, and to the evaluation of the likelihood of success in aldol reactions by which complex cyclic targets are prepared. [Pg.90]


See other pages where Aldol-like intramolecular cyclization is mentioned: [Pg.865]    [Pg.1982]    [Pg.1982]    [Pg.980]    [Pg.56]    [Pg.58]    [Pg.715]    [Pg.110]    [Pg.175]    [Pg.715]    [Pg.715]    [Pg.715]    [Pg.585]    [Pg.35]    [Pg.636]    [Pg.379]   
See also in sourсe #XX -- [ Pg.168 ]




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Aldol cyclizations

Aldol-like intramolecular

Cyclizations intramolecular

Intramolecular Aldolizations

Intramolecular aldol

Intramolecular aldol cyclization

Intramolecular aldol cyclizations

Intramolecular cyclization

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