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2-aryl-1-alkanol epoxide

Aliphatic aldehydes react with I in the presence of HMPT to form l-(trimethylsilyl)-l-alkanols, RCH(OH)Si(CH,), in 30-70% yield. Aryl aldehydes are converted into pin-acols by reaction with 1, generally in high yield. Ketones and epoxides are inert to 1. [Pg.461]

See other pages where 2-aryl-1-alkanol epoxide is mentioned: [Pg.2161] [Pg.2161] [Pg.2264] [Pg.2265] [Pg.2298] [Pg.1102] [Pg.607]

See also in sourсe #XX -- [ Pg.99 , Pg.133 , Pg.1046 , Pg.1047 , Pg.1048 , Pg.1052 ]

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Aryl epoxides