Covering: 2012 to 2013. Previous review: Nat. Prod. Rep., 2013, 30, 694–752 This review
covers the literature on simple indole alkaloids and those with a nonrearranged …

Biomass resources have infinite possibilities for introducing nitrogen, sulfur, or phosphorus
heteroatoms into their structures by virtue of controllable carbon–heteroatom bond …

The widespread use of transition‐metal‐mediated C− H bond activation has altered the field
of organic synthesis. Notwithstanding the immense effect this strategy has had on classical …

An efficient, green, and novel method for the synthesis of N-heterocycle-fused quinoxalines
is reported herein. Dimethyl sulfoxide was used as both a reactant and a solvent in this …

Fused tetracyclic systems containing a quinoline nucleus represent an important class of
heterocyclic bioactive natural products and pharmaceuticals because of their significant and …

Abstract γ-Carboline alkaloids are a family of natural and synthetic agents that have diverse
bioactivities including antiviral, antibacterial, antifungal, antiparasitic, antitumor, anti …

Abstract The indoloquinoline alkaloids cryptolepine (1), neocryptolepine (2), isocryptolepine
(3), and isoneocryptolepine (4) are important tools in traditional medicine. Now, their …

The Beckmann rearrangement of ketoximes, mediated by ammonium persulfate-dimethyl
sulfoxide as a reagent, has been achieved under neutral conditions. Based on the radical …

Here we report a protocol to synthesize diversiform fluorinated isocryptolepine analogues
with potential biological activities in one step via directed C-2 and C-3 dual C–H …

Novel isocryptolepine analogues have been conveniently synthesized and evaluated for
antimalarial and antiproliferative activities. We have found 3-fluoro-8-bromo-isocryptolepine …