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 …

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

Unprecedented tert-BuOK-mediated one carbon deletion of indoline hemiaminals has been
achieved. This novel protocol provides an efficient synthetic tool for the construction of 2 …

An I2/TBHP-mediated intramolecular dehydrogenative coupling reaction is developed for
the synthesis of a library of medicinally important 5, 11-dialkylindolo [3, 2-c] quinoline salts …

The widely varying different approaches to the total synthesis of the indoloquinoline alkaloid
neocryptolepine are discussed. Aspects relating to the isolation of the natural product from …

A facile approach to 6-aryl/alkyl substituted 6 H-indolo [2, 3-b] quinolines from mono-N-
substituted isoindigo derivatives in the presence of SnCl2· 2H2O in acid media is described …

The review summarizes the approaches to the synthesis of natural biologically active
indoloquinoline systems isolated from Cryptolepis sanguinolenta published over the past …

A convenient approach toward the indoloquinolines neocryptolepine and 6-
methylquinindoline from a common intermediate, is reported. Both sequences, designed for …

The tetracyclic indoloquinoline alkaloids, cryptolepine, neocryptolepine, isocryptolepine and
their analogues, isolated from the West African shrub Cryptolepis sanguinolenta are known …

A simple, straightforward and efficient method for the synthesis of a series of 11-methyl-6H-
indolo [2, 3-b] quinolines bearing different substituents on the indole and quinoline rings is …