Substituted piperazines and morpholines are valuable structural motifs in biologically active compounds, but are not easily prepared by contemporary cross-coupling approaches. In this report, we introduce SnAP reagents for the transformation of aldehydes into <i>N</i>-unprotected piperazines and morpholines. This approach offers simple, mild conditions compatible with aromatic, heteroaromatic, aliphatic, and glyoxylic aldehydes and provides mono- and disubstituted N-heterocycles in a single step
A simple and efficient one-pot three-component synthetic route to highly substituted and functionali...
Aldehydes are easily transformed into vicinal diamines and piperazines through a one-pot procedure i...
A one-pot Knoevenagel reaction/asymmetric epoxidation/domino ring-opening cyclization (DROC) has bee...
The precise placement of C-substituents on bicyclic and spirocyclic N-heterocycles is readily achiev...
A short, high yielding protocol has been developed for the enantioselective and general synthesis of...
Saturated N-heterocycles, for example, piperidines, piperazines, or morpholines can be found with in...
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 ...
The combination of cyclic ketones and stannyl amine protocol (SnAP) reagents affords saturated, spir...
Aldehydes are easily transformed into vicinal diamines and piperazines through a one-pot procedure i...
By using cheap and innocuous reagents, such as NaClO2, NaOCl, and catalytic amounts of TEMPO, a new ...
Piperazine ranks within the top three most utilized N-heterocyclic moieties in FDA-approved small-mo...
Addition of carbon nucleophiles to aldehyde tosylhydrazones of aromatic and heteroaromatic compounds...
[[abstract]]A series of monosubstituted piperazine derivatives were obtained by the reaction of pipe...
The metal-free synthesis of 2-substituted and 2,3-disubstituted morpholines through a one-pot strate...
A simple and efficient one-pot three-component synthetic route to highly substituted and functionali...
Aldehydes are easily transformed into vicinal diamines and piperazines through a one-pot procedure i...
A one-pot Knoevenagel reaction/asymmetric epoxidation/domino ring-opening cyclization (DROC) has bee...
The precise placement of C-substituents on bicyclic and spirocyclic N-heterocycles is readily achiev...
A short, high yielding protocol has been developed for the enantioselective and general synthesis of...
Saturated N-heterocycles, for example, piperidines, piperazines, or morpholines can be found with in...
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 ...
The combination of cyclic ketones and stannyl amine protocol (SnAP) reagents affords saturated, spir...
Aldehydes are easily transformed into vicinal diamines and piperazines through a one-pot procedure i...
By using cheap and innocuous reagents, such as NaClO2, NaOCl, and catalytic amounts of TEMPO, a new ...
Piperazine ranks within the top three most utilized N-heterocyclic moieties in FDA-approved small-mo...
Addition of carbon nucleophiles to aldehyde tosylhydrazones of aromatic and heteroaromatic compounds...
[[abstract]]A series of monosubstituted piperazine derivatives were obtained by the reaction of pipe...
The metal-free synthesis of 2-substituted and 2,3-disubstituted morpholines through a one-pot strate...
A simple and efficient one-pot three-component synthetic route to highly substituted and functionali...
Aldehydes are easily transformed into vicinal diamines and piperazines through a one-pot procedure i...
A one-pot Knoevenagel reaction/asymmetric epoxidation/domino ring-opening cyclization (DROC) has bee...