Tetrahydroquinoline is one of the most important simple nitrogen heterocycles, being
widespread in nature and present in a broad variety of pharmacologically active …

In recent decades, transition-metal-catalyzed nucleophilic dearomatization of electron-
deficient heteroarenes, such as pyridines, quinolines, isoquinolines and nitroindoles, has …

A highly enantioselective copper‐catalyzed alkynylation of quinolinium salts is reported. The
reaction employs StackPhos, a newly developed imidazole‐based chiral biaryl P, N ligand …

A highly enantioselective rhodium (I)‐catalyzed dearomative arylation or alkenylation of
easily available N‐alkylquinolinium salts is reported, thus providing an effective and …

The asymmetric syntheses of all members of the Hancock alkaloid family based upon a 2-
substituted N-methyl-1, 2, 3, 4-tetrahydroquinoline core are delineated. The conjugate …

A review of the isolation, reported methods for the synthesis (up to the end of 2018), and
spectroscopic data of angustureine, cuspareine, galipinine, and galipeine, members of the …

1, 2, 3, 4-Tetrahydroquinolines (THQs) are present in molecules with significant biological
importance and pharmaceuticals with diverse biological activities. Various synthetic routes …

The 1H and 13C NMR data of synthetic samples of (S)-N (1)-methyl-2-[2′-(3 ″-hydroxy-4
″-methoxyphenyl) ethyl]-1, 2, 3, 4-tetrahydroquinoline, the originally proposed structure of …

The present study describes the total synthesis of 1, 2, 3, 4-tetrahydroquinoline alkaloids (±)-
galipinine,(±)-cuspareine,(±)-galipeine and (±)-angustureine, in three steps and high yields …

A stereoselective approach for the synthesis of haliclamide 1, a marine natural product, has
been developed. The notable features of our synthesis include MacMillan cross aldol …