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GRIECO Reagent

A. Krief, A.-M. Laval, Ortho-Nitrophenyl Selenocyanate, a Valuable Reagent in Organic Synthesis Application to One of the Most Powerful Routes to Terminal Olefins from Primary-Alcohols (The Grieco-Sharpless Olefination Reaction) and to the Regioselective Isomerization of Allyl Alcohols), ... [Pg.101]

A. Krief and A.-M. Laval, u-Nitrophenyl selenocyanate, a valuable reagent in organic synthesis Application to one of the most powerful routes to terminal olefins from primary-alcohols (the Grieco-Sharpless olefination reaction) and to the regioselective isomerization of allyl alcohols, Bull. Soc. Chim. Fr. 1997,13, 869-874. [Pg.84]

In 1977, Grieco et al. employed benzeneperoxyseleninic acid (495) generated in situ from benzeneseleninic acid (494) and hydrogen peroxide (541). The peroxy acid was employed in overstoichiometric amounts as reagent for the Baeyer-Villiger reaction (Scheme 7.84) [355],... [Pg.297]

See other pages where GRIECO Reagent is mentioned: [Pg.79]    [Pg.453]    [Pg.137]    [Pg.79]    [Pg.79]    [Pg.137]    [Pg.385]    [Pg.79]    [Pg.453]    [Pg.137]    [Pg.79]    [Pg.79]    [Pg.137]    [Pg.385]    [Pg.1165]    [Pg.1367]    [Pg.307]    [Pg.866]    [Pg.1022]    [Pg.383]    [Pg.131]    [Pg.9]    [Pg.1234]    [Pg.1028]    [Pg.62]    [Pg.84]    [Pg.239]    [Pg.236]    [Pg.375]    [Pg.208]    [Pg.410]    [Pg.227]    [Pg.104]    [Pg.105]    [Pg.253]    [Pg.91]   
See also in sourсe #XX -- [ Pg.150 ]

See also in sourсe #XX -- [ Pg.137 ]

See also in sourсe #XX -- [ Pg.150 ]

See also in sourсe #XX -- [ Pg.150 ]

See also in sourсe #XX -- [ Pg.137 ]

See also in sourсe #XX -- [ Pg.385 ]



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