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2.2.2- Trichloroethyl carbamates protect amines

Troc protecting groups are easy to remove, which is an advantage associated with the use of 2,2,2-trichloroethyl-A/-tosyloxy-carbamate as a nitrene precursor cort5)ared to arylsulfamate, which require harsh reaction conditions to obtain the free amine. Both amantadine (R = H) and memantine (R = Me) hydrochloride were prepared in quantitative yields from the corresponding Troc-protected amino compounds (eq 5). ... [Pg.571]


See other pages where 2.2.2- Trichloroethyl carbamates protect amines is mentioned: [Pg.156]    [Pg.407]    [Pg.509]   
See also in sourсe #XX -- [ Pg.510 , Pg.617 ]




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2- carbamates protect amines

2.2.2- Trichloroethyl carbamates

Amine protection carbamate

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