反応式
[S-][C:2]#[N:3].[NH4+].[C:5]([OH:8])(=[O:7])[CH3:6].F[C:10](F)(F)[C:11]([OH:13])=O.[C:16](OC(=O)C)(=O)[CH3:17]>C(N(CC)CC)C>[C:11]([N:3]1[CH2:2][CH2:17][CH2:16][C@H:6]1[C:5]([OH:8])=[O:7])(=[O:13])[CH3:10]参加物
6
実験手順
ammonium thiocyanate (BDH, Analar), Aristar acetic acid (BDH), eptide synthesis grades of trifluoroacetic acid and acetic anhydride (Applied Biosystems) were used without further purification. Reagents for amino acid analysis of phenylthiocarbamyl amino acids were all of the highest possible purity (Inglis et al Biochem. Biophys. Methods 15:249, 1988). Pierce 6M constant boiling HC1 and Analar phenol (BDH) were used for hydrolysis and N,N-diisopropylethylamine (DIEA, Peptide Synthesis Grade, Applied Biosystems) replaced triethylamine in the drying reagent and in the coupling buffer.
後処理
- customwere used without further purification
- customand Analar phenol (BDH) were used for hydrolysis and N,N-diisopropylethylamine (DIEA, Peptide Synthesis Grade, Applied Biosystems)
出典と根拠
- ORDレコード
- ord-34e412f94b714d90839c31b45566e546
- 出典データセット
- uspto-grants-1998_05
- 特許番号
- US05756667
関連ノート
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