On September 24, 2021, Reddy, V. Veerabadhra; Reddy, B. V. Subba published an article.Product Details of 79815-20-6 The title of the article was Azomethine ylide cycloaddition of 2-C-formyl glycals with α-amino acids for the synthesis of substituted pyrroles. And the article contained the following:
A novel strategy has been devised for the synthesis of pyrrole based acyclo-C-nucleosides, in particular an open-chain sugar substituted pyrrole derivatives by means of the condensation of 2-C-formyl glycals with α-amino acids through an intramol. azomethine cycloaddition under thermal conditions. The use of cyclic α-amino acids provides the corresponding bicyclic pyrrole derivatives This is a first report on the synthesis of pyrrole based acyclo-C-nucleosides. The experimental process involved the reaction of H-Idc-OH(cas: 79815-20-6).Product Details of 79815-20-6
The Article related to pyrrole acyclo nucleoside preparation, formyl glycal alpha amino acid condensation azomethine ylide cycloaddition, Heterocyclic Compounds (One Hetero Atom): Pyrroles and Pyrrolizines and other aspects.Product Details of 79815-20-6
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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