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Direct cycloauration reactions

One of the most facile, direct cycloauration reactions is that of an [AuC14] source with (commercially available) 2-anilinopyridine. Reaction of Na[AuCl4] with... [Pg.223]

As described in Section II.A, the complex 2-(3-thienyl)pyridineAuCl3 6 undergoes direct cycloauration in refluxing MeCN/H20, but the 2-thienyl isomer 7 does not.14 However, reaction of 7 with Ag[BF4] in dichloromethane did give the desired product 9. [Pg.211]

However, cycloauration is, sometimes, difficult to achieve with direct activation of a C—H bond and transmetallation reaction of organomercury or organotin compounds with the appropriate gold compounds is, hence, frequently used. This procedure has been used with azobenzene, 36 A, A -dimethylbenzilamine,1937,1938 4,4 -dimethyl-2-phenyl-l, 3-oxaazoline,1938 1 - (dii zene,... [Pg.1011]


See other pages where Direct cycloauration reactions is mentioned: [Pg.207]    [Pg.207]    [Pg.209]    [Pg.209]    [Pg.210]    [Pg.211]    [Pg.213]    [Pg.223]    [Pg.225]    [Pg.145]    [Pg.207]    [Pg.207]    [Pg.209]    [Pg.209]    [Pg.210]    [Pg.211]    [Pg.213]    [Pg.223]    [Pg.225]    [Pg.145]    [Pg.208]    [Pg.217]    [Pg.225]    [Pg.226]    [Pg.228]    [Pg.214]    [Pg.222]   
See also in sourсe #XX -- [ Pg.209 , Pg.210 , Pg.213 , Pg.223 ]




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Cycloauration

Direct reactions

Directed reactions

Reaction cycloauration

Reaction direct reactions

Reaction direction

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