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Epoxy alcohol ring opening intramolecular nucleophile

The site of attack can also be directed by functionality on the substrate itself, as in the phenyl-boronate-mediated C-2 selective azide ring-opening reaction of trans-2,3-epoxy alcohols (82) by sodium azide. In this reaction, the nucleophile is delivered intramolecularly fiom the azidoboronate intermediate 83. Yields are generally good to excellent <99TL4589>. [Pg.66]

See other pages where Epoxy alcohol ring opening intramolecular nucleophile is mentioned: [Pg.301] [Pg.272] [Pg.207] [Pg.282] [Pg.338] [Pg.338] [Pg.255] [Pg.357] [Pg.58] [Pg.67] [Pg.68] [Pg.338]

See also in sourсe #XX -- [ Pg.207 , Pg.208 , Pg.209 ]

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Alcohols epoxy, ring opening

Alcohols nucleophiles

Alcohols nucleophilicity

Alcohols opening

Epoxy alcohols

Epoxy ring

Intramolecular nucleophilic ring-opening

Intramolecular opening

Nucleophile alcohols

Nucleophile intramolecular

Nucleophiles opening

Nucleophilic alcohols

Nucleophilic intramolecular

Nucleophilic ring opening