The combination of cyclic ketones and stannyl amine protocol (SnAP) reagents affords saturated, spirocyclic N-heterocycles under operationally simple reaction conditions. The resulting, <i>N</i>-unprotected spirocyclic amines are in great demand as scaffolds for drug discovery and development. The union of SnAP reagents and acyclic trifluoromethylketones yields α-CF<sub>3</sub> morpholines and piperazines
International audienceGold-(I) catalysis was used for the intramolecular cyclization of tertiary alc...
An efficient strategy for the synthesis of spiro-pyrrolopyridazines has been developed. When reacted...
Presented herein is a controllable selective construction of spiro or fused heterocyclic scaffolds t...
The combination of cyclic ketones and stannyl amine protocol (SnAP) reagents affords saturated, spir...
The precise placement of C-substituents on bicyclic and spirocyclic N-heterocycles is readily achiev...
Saturated N-heterocycles, for example, piperidines, piperazines, or morpholines can be found with in...
A variety of spirocyclic heterocycles have been constructed by a double-alkylation and reductive cyc...
Abstract: A new strategy from simple cyclic β-ketoesters or amides involving a selective three-compo...
The tachykinins are a family of neuropeptides found in the body that have been implicated in a varie...
A general two-step synthesis of 2-spiropiperidines has been developed. δ-Amino-β-ketoesters can be r...
Commercially available tin amine protocol (SnAP) reagents provide a simple approach to the synthesis...
Substituted piperazines and morpholines are valuable structural motifs in biologically active compou...
This report describes the preparation of a series of 17 novel racemic spirocyclic scaffolds that are...
A heterocyclic, sp3-rich chemical scaffold was synthesised in just 6 steps via a highly regio- and d...
International audienceThe reaction between cyclic 1,3-ketoamides and Michael acceptors in the presen...
International audienceGold-(I) catalysis was used for the intramolecular cyclization of tertiary alc...
An efficient strategy for the synthesis of spiro-pyrrolopyridazines has been developed. When reacted...
Presented herein is a controllable selective construction of spiro or fused heterocyclic scaffolds t...
The combination of cyclic ketones and stannyl amine protocol (SnAP) reagents affords saturated, spir...
The precise placement of C-substituents on bicyclic and spirocyclic N-heterocycles is readily achiev...
Saturated N-heterocycles, for example, piperidines, piperazines, or morpholines can be found with in...
A variety of spirocyclic heterocycles have been constructed by a double-alkylation and reductive cyc...
Abstract: A new strategy from simple cyclic β-ketoesters or amides involving a selective three-compo...
The tachykinins are a family of neuropeptides found in the body that have been implicated in a varie...
A general two-step synthesis of 2-spiropiperidines has been developed. δ-Amino-β-ketoesters can be r...
Commercially available tin amine protocol (SnAP) reagents provide a simple approach to the synthesis...
Substituted piperazines and morpholines are valuable structural motifs in biologically active compou...
This report describes the preparation of a series of 17 novel racemic spirocyclic scaffolds that are...
A heterocyclic, sp3-rich chemical scaffold was synthesised in just 6 steps via a highly regio- and d...
International audienceThe reaction between cyclic 1,3-ketoamides and Michael acceptors in the presen...
International audienceGold-(I) catalysis was used for the intramolecular cyclization of tertiary alc...
An efficient strategy for the synthesis of spiro-pyrrolopyridazines has been developed. When reacted...
Presented herein is a controllable selective construction of spiro or fused heterocyclic scaffolds t...