The morpholine and piperazine with their remarkable physical and biochemical properties are popular heterocycles in organic and medicinal chemistry used in rational property design. However, in the majority of cases these rings are added to an existing molecule in a building block approach thus limiting their substitution pattern and diversity. Here we introduce a versatile de novo synthesis of the morpholine and piperazine rings using multicomponent reaction chemistry. The large scale amenable building blocks can be further substituted at up to four positions, making this a very versatile scaffold synthesis strategy. Our methods thus fulfill the increasing demand for novel building block design and nontraditional scaffolds which previously...
An efficient synthesis of 2,2,6-trisubstituted morpholine is described which involves a multicompone...
It is well known that the field of modern organic chemistry has been developing extremely fast. Th...
Ring-opening of cyclic sulfamidates with propargylic sulfonamides yielded substrates for a gold-cata...
The morpholine and piperazine with their remarkable physical and biochemical properties are popular ...
The morpholine and piperazine with their remarkable physical and biochemical properties are popular ...
Piperazine scaffolds are amongst the most extensively used backbones in medicinal chemistry and many...
The synthesis of large numbers of diverse molecular scaffolds with controlled molecular properties i...
Substituted piperazines and morpholines are valuable structural motifs in biologically active compou...
Piperazine ranks within the top three most utilized N-heterocyclic moieties in FDA-approved small-mo...
The precise placement of C-substituents on bicyclic and spirocyclic N-heterocycles is readily achiev...
Piperazines are widely used as central elements in the construction of bioactive molecules. Herein, ...
By emulating the universal biosynthetic strategy, which employs modular assembly and divergent cycli...
One of the main directions in the development of modern organic chemistry is to increase the effic...
A cascade, metal promoted transformations utilizing chloro allenylamide, primary amine and aryl iodi...
The activity of pharmacologically active compounds can be increased by presenting a drug in a define...
An efficient synthesis of 2,2,6-trisubstituted morpholine is described which involves a multicompone...
It is well known that the field of modern organic chemistry has been developing extremely fast. Th...
Ring-opening of cyclic sulfamidates with propargylic sulfonamides yielded substrates for a gold-cata...
The morpholine and piperazine with their remarkable physical and biochemical properties are popular ...
The morpholine and piperazine with their remarkable physical and biochemical properties are popular ...
Piperazine scaffolds are amongst the most extensively used backbones in medicinal chemistry and many...
The synthesis of large numbers of diverse molecular scaffolds with controlled molecular properties i...
Substituted piperazines and morpholines are valuable structural motifs in biologically active compou...
Piperazine ranks within the top three most utilized N-heterocyclic moieties in FDA-approved small-mo...
The precise placement of C-substituents on bicyclic and spirocyclic N-heterocycles is readily achiev...
Piperazines are widely used as central elements in the construction of bioactive molecules. Herein, ...
By emulating the universal biosynthetic strategy, which employs modular assembly and divergent cycli...
One of the main directions in the development of modern organic chemistry is to increase the effic...
A cascade, metal promoted transformations utilizing chloro allenylamide, primary amine and aryl iodi...
The activity of pharmacologically active compounds can be increased by presenting a drug in a define...
An efficient synthesis of 2,2,6-trisubstituted morpholine is described which involves a multicompone...
It is well known that the field of modern organic chemistry has been developing extremely fast. Th...
Ring-opening of cyclic sulfamidates with propargylic sulfonamides yielded substrates for a gold-cata...