Indolizine (pyrrolo [1, 2-a] pyridine) is one of the five isomers of indole and it serves as a
precursor for widespread indolizidine alkaloids. The straightforward synthesis of indolizines …

Human DNA cytosine-to-uracil deaminases catalyze mutations in both pathogen and
cellular genomes. APOBEC3D, APOBEC3F, APOBEC3G, and APOBEC3H restrict human …

The ability to regulate and even target mutagenesis is an extremely valuable cellular asset.
Enzyme-catalyzed DNA cytosine deamination is a molecular strategy employed by …

Abstract Human APOBEC3G (apolipoprotein B mRNA-editing enzyme, catalytic polypeptide-
like 3G, A3G) is a potent restriction factor against human immunodeficiency virus type 1 (HIV …

A cost-effective, highly regioselective and metal-free version for the synthesis of indolizine
derivatives by means of Tf2O-mediated cascade reaction of pyridyl-enaminones and …

Here we present a novel annulation of pyridinium salts with BrCF2CO2Et to access the
indolizine derivatives with high efficiency. The α substitution of pyridine plays a key role in …

Introduction Indolizines are structural isomers with indoles. Although several indole-based
commercial drugs are available in the market, none of the indolizine-based drugs are …

The first highly regio-and enantioselective synthesis of 3-allylindolizines has been
developed by the sequential Rh-catalyzed asymmetric allylation and Tschitschibabin …

Indolizine derivatives are prevalent in many synthetic intermediates, pharmaceuticals, and
organic materials. Herein, we report a novel electro-oxidative cascade cyclization reaction …

Iron-Catalyzed Aerobic Oxidation and Annulation Reaction of Pyridine and α-Substituted Allenoate
toward Functionalized Indolizine | Organic Letters ACS ACS Publications C&EN CAS Find my …