Gas Chromatography

Building block for introduction of typtophan by Fmoc SPPS. Superceded by Fmoc-Trp(Boc)-OH.

Building block for introduction of typtophan by Fmoc SPPS. Superceded by Fmoc-Trp(Boc)-OH.

Building block for introduction of typtophan by Fmoc SPPS. Superceded by Fmoc-Trp(Boc)-OH.

The side-chain ClTrt group can be removed with 1% TFA/ 5% TIS in DCM, enabling the side-chain hydroxyl group to be selectively modified whilst the derivative is attached to the solid support during Fmoc SPPS. Associated Protocols and Technical

The side-chain ClTrt group can be removed with 1% TFA/ 5% TIS in DCM, enabling the side-chain hydroxyl group to be selectively modified whilst the derivative is attached to the solid support during Fmoc SPPS. Associated Protocols and Technical

Standard building block for introduction of O-methyl-tyrosine amino-acid residues by Fmoc SPPS Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Fmoc SPPS Linkage Replaces: 04-12-1118 Analysis Note Color (visual):

Fmoc-Tyr(PO(NMe 2 ) 2 )-OH is a useful derivative for the synthesis of phosphotyrosine-containing peptides by Fmoc SPPS [1] . As the side-chain phosphate group is fully protected, this derivative is compatible with all coupling methods.

An excellent building block for the preparation of phosphotyrosine-containing peptides [1] by Fmoc SPPS. This derivative can be introduced using standard activation methods, such as PyBOP &#174 and TBTU.

A useful derivative for the synthesis of phosphotyrosine peptides [1,2,3,4,5,67] by Fmoc SPPS. Pyrophosphate formation has been noted in peptides containing adjacent Tyr(PO 3 H 2 ) residues [4,5] .

A useful derivative for the synthesis of phosphotyrosine peptides [1,2,3,4,5,67] by Fmoc SPPS. Pyrophosphate formation has been noted in peptides containing adjacent Tyr(PO 3 H 2 ) residues [4,5] .

A useful derivative for the synthesis of phosphotyrosine peptides by the global Fmoc SPPS phosphorylation methodology [1] . Associated Protocols and Technical Articles Cleavage and Deprotection Protocols for Fmoc SPPS Literature references [1] E.

A cysteine-based pseudoproline dipeptide. It prevents aggregation during Fmoc SPPS and enhances product purity in an identical manner to standard pseuproline dipeptides.