Regioselective Hydrodebromination of Polybrominated Indoles
G Chelucci, GA Pinna, G Pinna
Index: Chelucci, Giorgio; Pinna, Gerard A.; Pinna, Giansalvo European Journal of Organic Chemistry, 2014 , vol. 2014, # 18 p. 3802 - 3807
Full Text: HTML
Citation Number: 0
Abstract
Abstract The mixture of sodium borohydride and N, N, N′, N′-tetramethylethylenediamine in combination with a palladium catalyst is a mild and efficient system for the regioselective hydrodebromination of polybrominated indoles with both N-donating and N-withdrawing substituents [N-methyl-and N-(methoxycarbonyl) indoles, respectively].
Related Articles:
Synthesis and biological activities of isogranulatimide analogues
[Hugon, Bernadette; Anizon, Fabrice; Bailly, Christian; Golsteyn, Roy M.; Pierre, Alain; Leonce, Stephane; Hickman, John; Pfeiffer, Bruno; Prudhomme, Michelle Bioorganic and Medicinal Chemistry, 2007 , vol. 15, # 17 p. 5965 - 5980]
Synthesis of bromoindole alkaloids from Laurencia brongniartii
[Suarez-Castillo, Oscar R.; Beiza-Granados, Lidia; Melendez-Rodriguez, Myriam; Alvarez-Hernandez, Alejandro; Morales-Rios, Martha S.; Joseph-Nathan, Pedro Journal of Natural Products, 2006 , vol. 69, # 11 p. 1596 - 1600]