A Regioselective Synthesis Method of Tri- and Tetrahalogenoindoles and Its Application for the Total Syntheses of Marine Alkaloids

A Regioselective Synthesis Method of Tri- and Tetrahalogenoindoles and Its Application for the Total Syntheses of Marine Alkaloids Polyhalogenated Indoles from the Red Alga <i>Rhodophyllis membranacea</i>: The First Isolation of Bromo-Chloro-Iodo Secondary Metabolites Isolation, Synthetic Studies and Biological Activities of the Marine Triindole Alkaloids Pseudellone C, Metagenetriindole A, Araiosamine A-D and Bengacarboline New synthetic approach to pyrroloiminoquinone marine alkaloids. Total synthesis of makaluvamines A, D, I, and K Synthesis of Indole Alkaloid Analogues:  Novel Domino Stereoselective Electrophile Addition−Cyclizations of Tryptophan-Derived α-Amino Nitriles Marine Indole Alkaloids Halogen Bond (XB) Promoted α-Tribromomethylation of N-Aryltetrahydroisoquinolines and Further Cyclization to 5,6-Dihydroindolo[2,1-a]isoquinolines Electrochemical collective synthesis of labeled pyrroloindoline alkaloids with Freon-type methanes as functional C1 synthons The Xanthate Route to Indolines, Indoles, and their Aza Congeners Design and synthesis of the novel antibacterial agent 8-bromo-1,1-dimethyl-1,3,4,9-tetrahydropyrano[3,4-b]indole and its derivatives