An efficient cascade transformation toward indolizine-based molecules has been developed. This process leads to the rapid construction of two C–N bonds and one C–C bond without the need of any metal catalysis. The approach involves easily accessible chromone-based Michael acceptors and propargylamine derivatives as starting materials. This cascade constitutes a novel and very competitive alternative to the well reported strategies using pyridine or pyrrole derivatives for accessing the indolizine ring with substituents at uncommon <i>C</i>-positions
A novel approach for the synthesis of indolizines from 2-(pyridin-2-yl)acetates, ynals, and alcohol...
An efficient, one-pot synthetic method for producing functionalized indolizine derivatives was devel...
An efficient, one-pot synthetic method for producing functionalized indolizine derivatives was devel...
Polysubstituted indolizine derivatives are constructed via intramolecular C--N bond formation/C--H b...
Polysubstituted indolizine derivatives are constructed via intramolecular C--N bond formation/C--H b...
A one-pot synthetic protocol involving 1,3-dipolar cycloaddition/deprotonation/elimination/oxidation...
A series of transition metal-free tandem reactions for the synthesis of indolizines and 6,7-dihydroi...
A unique strategy toward the synthesis of polysubstituted indolizines has been developed. When 2-pyr...
A new synthetic route to indolizines with various substituents on the pyridine moiety was developed ...
The cyclopentadiene–phosphine ligand (<b>L1</b>) and palladium were found to be an efficient catalys...
The cyclopentadiene–phosphine ligand (<b>L1</b>) and palladium were found to be an efficient catalys...
A novel copper/I<sub>2</sub>-mediated oxidative cross-coupling/cyclization of 2-(pyridin-2-yl)aceta...
Various indolizines are synthesized through one-pot, two-step 1,3-dipolar cycloadditions in recyclab...
Indolizines and pyrroles are considered as “privileged” structures since their skeletons were found ...
Indolizines and pyrroles are considered as “privileged” structures since their skeletons were found ...
A novel approach for the synthesis of indolizines from 2-(pyridin-2-yl)acetates, ynals, and alcohol...
An efficient, one-pot synthetic method for producing functionalized indolizine derivatives was devel...
An efficient, one-pot synthetic method for producing functionalized indolizine derivatives was devel...
Polysubstituted indolizine derivatives are constructed via intramolecular C--N bond formation/C--H b...
Polysubstituted indolizine derivatives are constructed via intramolecular C--N bond formation/C--H b...
A one-pot synthetic protocol involving 1,3-dipolar cycloaddition/deprotonation/elimination/oxidation...
A series of transition metal-free tandem reactions for the synthesis of indolizines and 6,7-dihydroi...
A unique strategy toward the synthesis of polysubstituted indolizines has been developed. When 2-pyr...
A new synthetic route to indolizines with various substituents on the pyridine moiety was developed ...
The cyclopentadiene–phosphine ligand (<b>L1</b>) and palladium were found to be an efficient catalys...
The cyclopentadiene–phosphine ligand (<b>L1</b>) and palladium were found to be an efficient catalys...
A novel copper/I<sub>2</sub>-mediated oxidative cross-coupling/cyclization of 2-(pyridin-2-yl)aceta...
Various indolizines are synthesized through one-pot, two-step 1,3-dipolar cycloadditions in recyclab...
Indolizines and pyrroles are considered as “privileged” structures since their skeletons were found ...
Indolizines and pyrroles are considered as “privileged” structures since their skeletons were found ...
A novel approach for the synthesis of indolizines from 2-(pyridin-2-yl)acetates, ynals, and alcohol...
An efficient, one-pot synthetic method for producing functionalized indolizine derivatives was devel...
An efficient, one-pot synthetic method for producing functionalized indolizine derivatives was devel...