Spontaneous spirocyclization of keto-sulfonamides via ynamides through a one-pot process is presented. Push–pull ynamides were obtained through Michael addition/elimination without Cu. The obtained azaspiro compounds are building blocks for indole alkaloids. Theoretical studies provide insights into the mechanism of the formal Conia-ene reaction
Indole-ynones have been established as general substrates for radical dearomatizing spirocyclization...
We have developed a short, efficient and enantioselective synthesis of 1,4,7,10-tetraoxa- and 1,7-di...
Abstract: The development of a new one-pot reaction sequence afforded the tricyclic core of several ...
Les travaux décrits dans ce manuscrit de thèse ont porté d'une part sur le développement de nouvelle...
Spirocyclization of keto-ynesulfonamides with quaternary ammonium salts was performed to access aza-...
Herein, we report an efficient synthesis of azaspiro[4,5]-decanes and azaspiro[4,5]-trienones by the...
Electron rich N-benzyl glyoxamides bearing at least two ipso-directing groups can be converted into ...
A novel and direct oxidative spirocyclization of arylpropiolamides with sulfonylhydrazides leading t...
The phosphine-catalyzed [3+2]-cycloaddition of the 2-methylene γ-lactams 4 and 5 and the acrylate 6 ...
A facile, efficient and unprecedented method for the synthesis of spiro-2H-pyrroles is reported. Whe...
Synthetic approaches toward multigram preparation of spirocyclic α,α-disubstituted pyrrolidines from...
Azaspirocycles are found as structural motif in a number of highly interesting natural products. In ...
A concise synthesis of spiro-cyclopropane compounds from indole derivatives and sulfur ylides has be...
A mild, reductive spirocyclization of indole-linked amides and lactams for the efficient and selecti...
A simple and general one-pot method for the synthesis of spiro-2 H -pyrroles has been developed. Ini...
Indole-ynones have been established as general substrates for radical dearomatizing spirocyclization...
We have developed a short, efficient and enantioselective synthesis of 1,4,7,10-tetraoxa- and 1,7-di...
Abstract: The development of a new one-pot reaction sequence afforded the tricyclic core of several ...
Les travaux décrits dans ce manuscrit de thèse ont porté d'une part sur le développement de nouvelle...
Spirocyclization of keto-ynesulfonamides with quaternary ammonium salts was performed to access aza-...
Herein, we report an efficient synthesis of azaspiro[4,5]-decanes and azaspiro[4,5]-trienones by the...
Electron rich N-benzyl glyoxamides bearing at least two ipso-directing groups can be converted into ...
A novel and direct oxidative spirocyclization of arylpropiolamides with sulfonylhydrazides leading t...
The phosphine-catalyzed [3+2]-cycloaddition of the 2-methylene γ-lactams 4 and 5 and the acrylate 6 ...
A facile, efficient and unprecedented method for the synthesis of spiro-2H-pyrroles is reported. Whe...
Synthetic approaches toward multigram preparation of spirocyclic α,α-disubstituted pyrrolidines from...
Azaspirocycles are found as structural motif in a number of highly interesting natural products. In ...
A concise synthesis of spiro-cyclopropane compounds from indole derivatives and sulfur ylides has be...
A mild, reductive spirocyclization of indole-linked amides and lactams for the efficient and selecti...
A simple and general one-pot method for the synthesis of spiro-2 H -pyrroles has been developed. Ini...
Indole-ynones have been established as general substrates for radical dearomatizing spirocyclization...
We have developed a short, efficient and enantioselective synthesis of 1,4,7,10-tetraoxa- and 1,7-di...
Abstract: The development of a new one-pot reaction sequence afforded the tricyclic core of several ...