This chapter is an update of the data on substrates, reactions, inducers, and inhibitors of
human CYP enzymes published previously by Rendic and DiCarlo Citation 1a, Citation 1b …

Breast cancer, a most common malignancy in women, was known to be associated with
steroid hormone estrogen. The discovery of estrogen receptor (ER) gave us not only a …

The present review describes the recent progress in synthetic approaches to construct
indolizine framework (including partially or wholly reduced ring) and the design of such …

The discovery of camptothecin and its analogs was the major breakthrough through which
“Indolizine moiety” came into limelight. Although major part of the research on indolizine …

Amongst nitrogen heterocycles of different ring sizes and oxidation statuses,
dihydropyridines (DHP) occupy a prominent role due to their synthetic versatility and …

A number of indolizines and pyrrolo [1, 2-a] quinolines/isoquinolines were prepared from
phenacyl pyridinium, quinolinium and isoquinolinium salts derived fromthe reaction of the …

In this study, a series of nitrogen‐based novel heterocyclic compounds were synthesized
and characterized by elemental analysis, IR and NMR spectra. The novel synthesized …

A novel palladium-catalyzed intermolecular aminocarbonylation of alkenes has been
developed in which the employment of hypervalent iodine reagent can accelerate the …

The inhibitory potency of ursolic acid extracted from Ilex paraguariensis, a plant used in
South American population for a tea preparation known as maté, and its derivatives to inhibit …

A protocol on chemoselective cobalt (II) porphyrin‐catalyzed intramolecular
cyclopropanation of N‐alkyl indoles/pyrroles with alkylcarbenes has been developed. The …