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9-Fluorenylmethyl carbamates

Methyl Carbamate 5. 9-Fluorenylmethyl Carbamate 8. 2,2,2-Trichloroethyl Carbamate 11. 2-Trimethylsilylethyl Carbamate 16. 1,1-Dimethylpropynyl Carbamate 20. 1-Methyl-1-phenylethyI Carbamate 22. 1-Methyl-l-(4-biphenylyl)ethyl Carbamate 24. 1,1 -Dimethy 1-2-haloethyl Carbamate 26. l,l-Dimethyl-2-cyanoethyl Carbamate 28. r-Butyl Carbamate... [Pg.441]

Fluorenylmethyl carbamate (Fmoc) is widely used in peptide chemistry and solid-phase peptide chemistry. Fmoc is often uniquely cleaved by amines and is stable under acidic conditions. [Pg.181]

Amine protection. Compared to simple 0-(9-fluorenylmethyl) carbamates, the t-butyl substituents make them more soluble. On deprotection by treatment with 20%... [Pg.161]

Moving ahead with this analysis, the retrosynthetic sword next cut the D-ring diketopiperazine ring of 6 (see Scheme 1) at the indicated amide linkage to reveal 7 as a protected amino acid precursor. Although the selection of a methyl ester and a 9-fluorenylmethyl carbamate (Fmoc) group to protect these new functionalities... [Pg.609]

Protecting groups commonly employed for masking amino groups include alkyl carbamates such as benzyl-, tert-butyl-, and 9-fluorenylmethyl carbamates. If used for the... [Pg.472]

See other pages where 9-Fluorenylmethyl carbamates is mentioned: [Pg.506]    [Pg.1082]    [Pg.69]    [Pg.412]    [Pg.166]    [Pg.241]    [Pg.452]    [Pg.202]    [Pg.69]    [Pg.711]    [Pg.1021]    [Pg.490]    [Pg.181]   


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9- fluorenylmethyl

9- fluorenylmethyl carbamates protect amines

Fluorenylmethyl Carbamates (Fmoc Protection)

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