108378-84-3Relevant academic research and scientific papers
Palladium Catalyzed Regioselective C4-Arylation and Olefination of Indoles and Azaindoles
Thrimurtulu, Neetipalli,Dey, Arnab,Singh, Anurag,Pal, Kuntal,Maiti, Debabrata,Volla, Chandra M. R.
supporting information, (2019/02/13)
A convergent strategy for the synthesis of biologically relevant C4-substituted indole scaffolds was demonstrated using Pd(II)-catalyzed remote C?H functionalization of indoles and azaindoles. The reaction displays high regioselectivity for the C4-positio
TIN-THALL REACTION, A VERSATILE METHOD FOR CROSS COUPLING TIN COMPOUNDS WITH THALLIUM COMPOUNDS
Somei, Masanori,Yamada, Fumio,Naka, Katsumi
, p. 1322 - 1326 (2007/10/02)
A new cross coupling reaction between tin compounds and thallium compounds is developed and its versatility is demonstrated by the convenient synthesis of various 4-substituted indoles.KEYWORDS - tin-thall reaction; thallation-palladation; cross coupling; 4-substituted indole; thallium compound; tin compound; palladium acetate; 4-(3-pyridyl)-3-indolecarbaldehyde
BORONATION-THALLATION, A NEW APPROACH TO THE SYNTHESIS OF INDOLES HAVING ARYL AND/OR A HETEROARYL SUBSTITUENT AT THE 4-POSITION
Somei, Masanori,Amari, Hirokuni,Makita, Yoshihiko
, p. 3971 - 3973 (2007/10/02)
A new coupling reaction for unsymmetrical biaryls was developed and applied successfully to the syntheses of 4-arylindoles.Photoreaction of 4-halogenoidoles also proved to be a useful method for preparing 4-substituted indoles.An alternative method for sy
