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Allyloxycarbonyl

Allylamines are difficult to cleave with Pd catalysts. Therefore, amines are protected as carbamates, but not as allylamines. Also, allyl ethers used for the protection of alcohols cannot be cleaved smoothly, hence alcohols are protected as carbonates. In other words, amines and alcohols are protected by an allyloxycarbonyl (AOC or Alloc) group. [Pg.382]

PdCl2(Ph3P)2, dimedone, THF, 95% yield. This method is also effective for removing the allyloxycarbonyl group from alcohols and amines. [Pg.248]

A Noble Metal-Sensitive Alternative Allyl Ester (All) and the Allyloxycarbonyl (Aloe) Croup... [Pg.374]

The selectivity and mildness of the Pd(0)-catalyzed deprotection of allyl (All) esters and the allyloxycarbonyl (Aloe) urethanes117 181 reaction also allowed for the successful and efficient application of this blocking group technology in the synthesis of acid- and base-labile lipidated pepti-... [Pg.374]

The combination of the N-terminal allyloxycarbonyl (Aloe) group (34) with the tert-butyl ester proved to be a particularly efficient tool in the synthesis of complex glycopeptides, as has been demonstrated in the synthesis of sensitive fucosyl chitobiose glycopeptides (19). The Aloe group was... [Pg.285]

H Kuntz, C Unverzagt. The allyloxycarbonyl (Aloe) moiety — conversion of an unsuitable into a valuable amino protecting group for peptide synthesis. Angew Chem Int Edn Engl 23, 436, 1984. [Pg.78]

O Dangles, F Guibe, G Balavoine, S Lavielle. A Marquet. Selective cleavage of the allyl and allyloxycarbonyl groups through palladium-catalyzed hydrostannolysis with tributyltin hydride. Application of the selective protection-deprotection of amino acid derivatives and in peptide synthesis. J Org Chem 52, 4984, 1987. [Pg.79]

T Vorherr, A Trzeciak, W Bannwart. Application of the allyloxycarbonyl protecting group for the indole of Trp in solid-phase peptide synthesis. Int J Pept Prot Res 48, 553, 1996. [Pg.169]

Synthesis of l,2-frans-2-Acetamido-2-deoxyglycosyl Amino Acids Using Carbamate (2,2,2-Trichloroethoxycarbonyl or Allyloxycarbonyl) Protection of the Amine... [Pg.268]


See other pages where Allyloxycarbonyl is mentioned: [Pg.335]    [Pg.382]    [Pg.44]    [Pg.481]    [Pg.481]    [Pg.793]    [Pg.793]    [Pg.797]    [Pg.272]    [Pg.315]    [Pg.629]    [Pg.161]    [Pg.381]    [Pg.109]    [Pg.294]    [Pg.100]    [Pg.66]    [Pg.78]    [Pg.90]    [Pg.161]    [Pg.168]    [Pg.547]    [Pg.578]    [Pg.187]    [Pg.180]    [Pg.181]    [Pg.234]    [Pg.282]    [Pg.316]    [Pg.79]    [Pg.294]    [Pg.372]    [Pg.711]   
See also in sourсe #XX -- [ Pg.345 , Pg.346 , Pg.436 , Pg.468 , Pg.540 ]

See also in sourсe #XX -- [ Pg.345 , Pg.346 , Pg.436 , Pg.468 , Pg.540 , Pg.575 ]




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Alcohols allyloxycarbonyl

Allyl Ethers and Allyloxycarbonyl Derivatives

Allyloxycarbonyl (Aloe)

Allyloxycarbonyl -protecting groups

Allyloxycarbonyl acetate

Allyloxycarbonyl group

Allyloxycarbonyl palladium

Allyloxycarbonyl protecting groups, cleavage

Allyloxycarbonyl, removal

Amines allyloxycarbonyl

Deprotection allyloxycarbonyl protecting groups

Deprotections allyloxycarbonyl groups

Esters allyloxycarbonyl

N-allyloxycarbonyl

Protecting allyloxycarbonyl

Protective groups allyloxycarbonyl

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