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Thiol Group Protection

4-aminobutyric acids where the N-protecting group can potentially [Pg.172]

Oppolzer, P.Dudfield, T.Stevenson, and T.Godel, Helv. Chim. Acta, 1985, [Pg.173]

For a general discussion of the RUO4 cleavage step, see S.Torii, T.Inokuchi, and K.Kondo, ibid., p. 4980. [Pg.173]

Helmchen, U.Leikauf, and I.Taufer-Knopfel, Angew, Chem., Int.Ed. Engl., 1985, 2, 874. [Pg.173]

Davies, l.M.Dordor-fledgecock, and P.Wamer, Tetrahedron Lett., 1985, 26, 2125. [Pg.173]

The base-catalyzed reaction of thiothreitol with methyl dithiobenzoate selectively protects a thiol group as an 5-thiobenzoyl derivative in the presence of a hydroxyl group.-... [Pg.298]

At pH 4-5, the reaction is selective for protection of thiol groups in the presence of oc- or e-amino groups. [Pg.301]

Meaciivny unart /. Protection for the Thiol Group Continued)... [Pg.439]

See other pages where Thiol Group Protection is mentioned: [Pg.77]    [Pg.303]    [Pg.172]    [Pg.552]    [Pg.270]    [Pg.270]    [Pg.77]    [Pg.303]    [Pg.172]    [Pg.552]    [Pg.270]    [Pg.270]    [Pg.203]    [Pg.239]    [Pg.104]    [Pg.490]    [Pg.277]    [Pg.278]    [Pg.279]    [Pg.279]    [Pg.280]    [Pg.282]    [Pg.284]    [Pg.286]    [Pg.288]    [Pg.290]    [Pg.292]    [Pg.294]    [Pg.296]    [Pg.298]    [Pg.299]    [Pg.300]    [Pg.302]    [Pg.304]    [Pg.306]    [Pg.308]    [Pg.437]    [Pg.438]    [Pg.455]    [Pg.456]    [Pg.456]    [Pg.457]    [Pg.458]    [Pg.460]    [Pg.462]    [Pg.464]    [Pg.466]   
See also in sourсe #XX -- [ Pg.647 ]



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