1195738-11-4Relevant articles and documents
One-pot total synthesis of streptindole, arsindoline B and their congeners through tandem decarboxylative deaminative dual-coupling reaction of amino acids with indoles
Xiang, Jiachen,Wang, Jungang,Wang, Miao,Meng, Xianggao,Wu, Anxin
, p. 4240 - 4247 (2015)
This paper described a decarboxylative deaminative dual-coupling reaction of amino acids with indoles to afford BIM scaffolds and its further application to the one-pot total synthesis of natural products. This method featured a stimulating example of activating amino acids in one pot as multi-carbon building blocks for transformation into final targets which are equipped with amino acid side chain backbones. This journal is
Facile access to bis(indolyl)methanes by copper-catalysed alkylation of indoles using alcohols under air
Nguyen, Ngoc-Khanh,Tran, Duc Long,Hung, Tran Quang,Le, Tra My,Son, Nguyen Thi,Trinh, Quang Thang,Dang, Tuan Thanh,Langer, Peter
supporting information, (2021/03/15)
Bis(3-indolyl)methanes (BIM) are important and present in the structure of many alkaloid and bioactive compounds (anti-inflammatory, anticancer, antiobesity, antimicrobial, etc.). Herein, we have reported an air stable and convenient Cu(OAc)2 c
Glycerin and CeCl3·7H2O: a new and efficient recyclable medium for the synthesis of bis(indolyl)methanes
Silveira, Claudio C.,Mendes, Samuel R.,Líbero, Francieli M.,Lenard?o, Eder J.,Perin, Gelson
experimental part, p. 6060 - 6063 (2010/03/03)
Glycerin and CeCl3·7H2O were successfully used in recyclable catalytic system for the synthesis of several bis(indolyl)methanes in good to excellent yields through the reaction of indoles with aldehydes. The method is applicable to a
