Yoo, Woo-Jin; Nguyen, Thanh V. Q.; Capdevila, Montse Guiteras; Kobayashi, Shu published the artcile< Lithium tert-butoxide-mediated carboxylation reactions of unprotected indoles and pyrroles with carbon dioxide>, SDS of cas: 23077-43-2, the main research area is indole carbon dioxide lithium butoxide Friedel Crafts type carboxylation; indolecarboxylic acid preparation; pyrrole carbon dioxide lithium butoxide Friedel Crafts type carboxylation; pyrrolecarboxylic acid preparation.
Unprotected indoles and pyrroles were found to underwent base-mediated carboxylation reactions under ambient pressure of carbon dioxide. It was found that this transition metal-free carboxylation reaction proceeded smoothly with the use of a large excess of LiOtBu.
Heterocycles published new progress about Aromatic carboxylic acids Role: RCT (Reactant), SPN (Synthetic Preparation), RACT (Reactant or Reagent), PREP (Preparation). 23077-43-2 belongs to class indole-building-block, and the molecular formula is C9H6FNO2, SDS of cas: 23077-43-2.
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