Ynamides were used as precursors for the in situ generation of highly reactive ketenimines which could be trapped with imines in a [2+2] cycloaddition. This imino Staudinger synthesis led to a variety of imino-analogs of β-lactams, namely azetidinimines (20 examples), that could be further functionalized through a broad range of transformations
Iminium ions and imines have been important for the synthesis of various organic molecules. The aim ...
The formal [2+2] cycloaddition of ketenes and imines, also known as Staudinger synthesis, is a facil...
The authors would like to acknowledge EPSRC for PhD funding through the Doctoral Training Schemes.Th...
International audienceYnamides were used as precursors for the in situ generation of highly reactive...
International audienceUsing ynamides as readily available starting materials, a single step can gene...
Complementary regioselective synthesis of iminohydantoins from isocyanoacetamides controlled by the ...
A quinone-mediated general synthetic platform for the construction of primary a-tertiary amines from...
Funding Information: Funding: This research was funded by the European Regional Development Fund, pr...
Studies to convert nitroalkanes into amides and esters using I2 and O2 revealed in situ-generated io...
Dihydroisoquinoline reacts with Danishefsky's diene under Lewis acidic conditions or neat, to give l...
The use of Direct Imine Acylation (DIA) methodology for the total synthesis of pallimamine is descri...
© 2016 The Chemical Society of Japan.Imines are among the most ubiquitous species in organic and bio...
As N-sulfenyl imines (e.g., RR‘CN−SAr) can be readily transformed to their N-sulfinyl imines (RR‘CN−...
Functionalized polycyclic aminopyridines are central to the chemical sciences, but their syntheses a...
The authors thank the Royal Society for a University Research Fellowship (ADS), the EU (IEF for CS) ...
Iminium ions and imines have been important for the synthesis of various organic molecules. The aim ...
The formal [2+2] cycloaddition of ketenes and imines, also known as Staudinger synthesis, is a facil...
The authors would like to acknowledge EPSRC for PhD funding through the Doctoral Training Schemes.Th...
International audienceYnamides were used as precursors for the in situ generation of highly reactive...
International audienceUsing ynamides as readily available starting materials, a single step can gene...
Complementary regioselective synthesis of iminohydantoins from isocyanoacetamides controlled by the ...
A quinone-mediated general synthetic platform for the construction of primary a-tertiary amines from...
Funding Information: Funding: This research was funded by the European Regional Development Fund, pr...
Studies to convert nitroalkanes into amides and esters using I2 and O2 revealed in situ-generated io...
Dihydroisoquinoline reacts with Danishefsky's diene under Lewis acidic conditions or neat, to give l...
The use of Direct Imine Acylation (DIA) methodology for the total synthesis of pallimamine is descri...
© 2016 The Chemical Society of Japan.Imines are among the most ubiquitous species in organic and bio...
As N-sulfenyl imines (e.g., RR‘CN−SAr) can be readily transformed to their N-sulfinyl imines (RR‘CN−...
Functionalized polycyclic aminopyridines are central to the chemical sciences, but their syntheses a...
The authors thank the Royal Society for a University Research Fellowship (ADS), the EU (IEF for CS) ...
Iminium ions and imines have been important for the synthesis of various organic molecules. The aim ...
The formal [2+2] cycloaddition of ketenes and imines, also known as Staudinger synthesis, is a facil...
The authors would like to acknowledge EPSRC for PhD funding through the Doctoral Training Schemes.Th...