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2- ethyl carbamate protect amines

Alkyl carbamates are generally more stable towards nucleophiles than amides, and are therefore of limited utility as protective groups. Amines lacking other base-sensitive functionalities can, however, be protected as alkyl carbamates. An illustrative example of the use of ethyl carbamate as a protective group is sketched in Figure 10.11 [188]. [Pg.293]

N, N-Dicyclohexylcarboxamido)ethyl carbamates, to protect amines, 326-327 /V-Diethoxymethylamines, to protect amines, 292... [Pg.236]

Ethyl disulfides, to protect thiols, 302 /V-(Ethyldithio) carbamates, to protect amines, 334... [Pg.238]

Methyl-1 -(4-biphenylyl)ethyl carbamates, to protect amines, 324-325, 326, 335 ( )-2-MethyI-2-butenoate (Tigloate) esters, to protect alcohols, 114 3-Methylbut-2-enyl ethers, to protect alcohols, 44, 45... [Pg.239]

See other pages where 2- ethyl carbamate protect amines is mentioned: [Pg.451]    [Pg.292]    [Pg.238]    [Pg.239]    [Pg.243]    [Pg.169]    [Pg.165]    [Pg.59]    [Pg.638]    [Pg.383]    [Pg.8]    [Pg.42]   
See also in sourсe #XX -- [ Pg.326 , Pg.342 ]

See also in sourсe #XX -- [ Pg.540 ]

See also in sourсe #XX -- [ Pg.326 ]



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1- Methyl-1- ethyl carbamates protect amines

2- carbamates protect amines

2- ethyl carbamates

2- ethyl carbamates, to protect amines

Amine protection carbamate

Ethyl amine

Ethyl protection

Ethyl, amine carbamate

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