SDS of cas: 59132-30-8On May 9, 1980 ,《Electrochemistry of natural products. 7. Oxidative decarboxylation of some tetrahydro-β-carbolinecarboxylic acids》 appeared in Journal of Organic Chemistry. The author of the article were Bobbitt, James M.; Willis, John P.. The article conveys some information:
A series of 1,2,3,4-tetrahydro-β-carboline-1- and -3-carboxylic acids containing various substituents in positions 1, 2, and 3 were oxidized electrochem. In general, the acids were decarboxylated, and unsaturation was introduced into the C ring. The oxidation appears to take place through the indole ring, N, and possible mechanisms of the reactions are given. Parallels between the observed reactions and early steps in indole alkaloid biosynthesis are discussed. The oxidative dimerization of tetrahydrocarbazole is reported. The experimental process involved the reaction of 2,3,4,9-Tetrahydro-1H-pyrido[3,4-b]indole-1,3-dicarboxylic acid(cas: 59132-30-8SDS of cas: 59132-30-8)
2,3,4,9-Tetrahydro-1H-pyrido[3,4-b]indole-1,3-dicarboxylic acid(cas: 59132-30-8) belongs to indole.The indole subunit is an almost ubiquitous component of biologically active natural products, and its study has been the focus of research for decades.SDS of cas: 59132-30-8They are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.
Referemce:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles