53924-07-5Relevant articles and documents
An efficient synthesis of medicinally important indole based triarylmethanes by using propylphosphonic anhydride (T3P)
Cheruku, Srinivas,Nagaraju, Chaithra,Shetty, Poornima,Hassan A, Swarup,Nagarakere C, Sandhya,Manikyanally N, Kumara,Kempegowda, Mantelingu
, p. 1486 - 1494 (2020)
We have developed an economical and efficient method for the synthesis of medicinally and synthetically important indole-based triarylmethanes by using indoles and benzhydrols in the presence of propylphosphonic anhydride (T3P). This methodolog
Palladium(II)-catalyzed efficient C-3 functionalization of indoles with benzylic and allylic alcohols under Co-catalyst, acid, base, additive and external ligand-free conditions
Das, Debjit,Roy, Sujit
, p. 1308 - 1314 (2013/06/26)
The bis(acetonitrile)palladium(II) chloride complex, PdCl 2(MeCN)2, efficiently catalyzes the regioselective alkylation of indoles with various benzylic and allylic alcohols under moisture and air insensitive conditions. Notably the
An efficient and general iron-catalyzed C-C bond activation with 1,3-dicarbonyl units as a leaving groups
Li, Huanrong,Li, Wenjuan,Liu, Weiping,He, Zhiheng,Li, Zhiping
supporting information; experimental part, p. 2975 - 2978 (2011/05/05)
(Chemical Equation Presented) With our compliments: The 1,3-dicarbonyl unit has been shown to be a new and useful leaving group for iron-catalyzed bond cleavage (see scheme). This new strategy can complement the traditional Friedel-Crafts reaction and was applied in the synthesis of indene derivatives.