A review. Propanephosphonic acid anhydride (T3P) is a prevailing coupling and dehydrating agent with many desirable properties which render it a reagent of choice for a plethora of reactions and, befittingly, its application in org. synthesis is rapidly increasing. Since its introduction as a peptide coupling agent in 1980, the realm of applications of T3P expanded. Currently its use showed a broad range of reactions, including condensation, functional group transformation, heterocycles prepn., rearrangements, and catalysis. It offers several advantages over traditional reagents, such as high yield, chem. and optical purity, broad functional group tolerance and easy work-up. The reagent is attractive for large-scale synthesis as well...
Abstractl-Proline has been used as an organocatalyst for an efficient synthesis of (α-aminoalkyl) ph...
In peptide synthesis, the issues related to poor sustainability, long reaction times and high proces...
AbstractTwo decades of domination of benzotriazole-based chemistry stimulated the progress in peptid...
Amidation is the predominant reaction within the pharmaceutical setting, and it is attracting greate...
A general, mild, efficient, and environmentally benign protocol, which makes use of T3P® as an acid ...
Amidation is the predominant reaction within the pharmaceutical setting, and it is attracting greate...
The purpose of medicinal chemistry is to efficiently create a variety of compounds with potential fo...
The synthesis of hydroxamic acids starting from carbox- ylic acids employing 1-propanephosphonic...
New, practical approaches for the synthesis of α-amino (2-alkynylphenyl)-methylphosphonates and 1,2-...
The reactions of triphenylphosphoranylidenesuccinic anhydride with amines, hydrazines and dipolar ni...
A high yield and rapid synthesis of enantiomerically pure N (alpha) -protected amino/peptide acid ar...
A high yield and rapid synthesis of enantiomerically pure N α -protected amino/peptide acid arylamid...
A simple and efficient method for the synthesis of alcohols from the corresponding carboxylic acids ...
A novel and mild protocol for the synthesis of phosphonotripeptide 16 were achieved from novel formy...
Synthesis of short peptides using propargyloxycarbonyl amino acid chlorides as effective coupling re...
Abstractl-Proline has been used as an organocatalyst for an efficient synthesis of (α-aminoalkyl) ph...
In peptide synthesis, the issues related to poor sustainability, long reaction times and high proces...
AbstractTwo decades of domination of benzotriazole-based chemistry stimulated the progress in peptid...
Amidation is the predominant reaction within the pharmaceutical setting, and it is attracting greate...
A general, mild, efficient, and environmentally benign protocol, which makes use of T3P® as an acid ...
Amidation is the predominant reaction within the pharmaceutical setting, and it is attracting greate...
The purpose of medicinal chemistry is to efficiently create a variety of compounds with potential fo...
The synthesis of hydroxamic acids starting from carbox- ylic acids employing 1-propanephosphonic...
New, practical approaches for the synthesis of α-amino (2-alkynylphenyl)-methylphosphonates and 1,2-...
The reactions of triphenylphosphoranylidenesuccinic anhydride with amines, hydrazines and dipolar ni...
A high yield and rapid synthesis of enantiomerically pure N (alpha) -protected amino/peptide acid ar...
A high yield and rapid synthesis of enantiomerically pure N α -protected amino/peptide acid arylamid...
A simple and efficient method for the synthesis of alcohols from the corresponding carboxylic acids ...
A novel and mild protocol for the synthesis of phosphonotripeptide 16 were achieved from novel formy...
Synthesis of short peptides using propargyloxycarbonyl amino acid chlorides as effective coupling re...
Abstractl-Proline has been used as an organocatalyst for an efficient synthesis of (α-aminoalkyl) ph...
In peptide synthesis, the issues related to poor sustainability, long reaction times and high proces...
AbstractTwo decades of domination of benzotriazole-based chemistry stimulated the progress in peptid...