The reagent Fmoc–OSu was proven to be the source of Fmoc–β-Ala–OH, following a mechanism that involved many deprotonation and elimination steps and a Lossen-type rearrangement as key sequence. The impurity Fmoc–β-Ala-OH was found in a variety of reactions in which Fmoc–OSu was ...
2,7-Di-tert-butyl-Fmoc-P-OSu: a new polymer-supported reagent for the protection of the amino group.Amino AcidsFluorenesOrganic ChemicalsPolymersSuccinimides2,7-di tert butyl-9-fluorenyl)methyl succinimidyl carbonate氨基酸类芴类有机化学品
The mechanism of action in peptide synthesis involves the selective deprotection of the Fmoc and Boc groups, allowing for the coupling of the protected amino acid to form a peptide chain. Storage Conditions: Store in a cool and dry place. View all ...
The mechanism of action in peptide synthesis involves the removal of the Fmoc protecting group and subsequent coupling reactions with other amino acids. Drug Discovery: This compound is also used in drug discovery research as a starting material for the synthesis of potential therapeutic agents. ...
The mechanism of action in organic synthesis involves the selective protection of the valine amino acid, allowing for specific reactions to occur without affecting the valine residue. Storage Conditions: Store in a cool and dry place. View all ...
The mechanism of action involves the FMOC group temporarily blocking the reactive amino group, allowing for selective reactions with other amino acids. This protects the cysteine residue and ensures the desired peptide sequence is obtained. Storage ConditionsStore FMOC-D-CYS(ACM)-OH in a cool ...