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Protective groups benzoyl

In the second procedure13 (see Scheme 3), D-glucitol (10) was converted into 5-O-benzoyl-1,3 2,4-di-O-ethyl idene-6-O-trityl-D-glucitol (17) by successive treatment with acetaldehyde to produce 15, with chlorotriphenylmethane to provide 16, and with benzoyl chloride to afford 17. Selective removal of the trityl protecting group from 17, to give 18, followed by oxidation of 18, provided 19 which, on hydrolysis, afforded L-gulose (9). [Pg.291]

Besides acetyl, benzoyl, and benzyl protecting groups for the carbohydrate hydroxyl groups, silyl, isopropylidene, and p-methoxybcnzyl groups have also been employed in solid-phase glycopeptide synthesis. The synthesis of a glycopeptide... [Pg.267]

Furthermore, attempted cyclization of N-carboxymethyl meroquinene ethyl ester failed to afford any of the enone, suggesting that the carboxylic acid was an intermediate. The N-protecting groups, in addition to benzoyl, that are tolerated include CC Me, pivaloyl, acetyl, toluenesulfonyl, CBz, and alkyl. [Pg.117]


See other pages where Protective groups benzoyl is mentioned: [Pg.23]    [Pg.422]    [Pg.150]    [Pg.711]    [Pg.23]    [Pg.422]    [Pg.150]    [Pg.711]    [Pg.220]    [Pg.220]    [Pg.224]    [Pg.349]    [Pg.383]    [Pg.384]    [Pg.550]    [Pg.227]    [Pg.157]    [Pg.129]    [Pg.1114]    [Pg.556]    [Pg.3]    [Pg.265]    [Pg.1250]    [Pg.871]    [Pg.77]    [Pg.105]    [Pg.108]    [Pg.178]    [Pg.105]    [Pg.1014]    [Pg.52]    [Pg.52]    [Pg.101]    [Pg.195]    [Pg.211]    [Pg.218]    [Pg.224]    [Pg.233]    [Pg.342]    [Pg.367]    [Pg.80]    [Pg.222]    [Pg.49]    [Pg.4]    [Pg.10]    [Pg.203]    [Pg.260]    [Pg.66]    [Pg.84]    [Pg.221]    [Pg.70]   
See also in sourсe #XX -- [ Pg.17 ]




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Benzoyl group

Benzoyl protecting groups

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