6915-66-8Relevant articles and documents
Metal-free synthesis of 1H-indole-2-carbaldehydes by N-iodosuccinimide- mediated cyclization of 1-(2′-anilinyl)prop-2-yn-1-ols in water. A formal synthesis of (R)-calindol
Kothandaraman, Prasath,Lauw, Sherman Jun Liang,Chan, Philip Wai Hong
, p. 7471 - 7480 (2013/08/23)
A N-iodosuccinimide (NIS)-mediated method to prepare 1H-indole-2- carbaldehydes efficiently from cycloisomerization of 1-(2-aminophenyl)prop-2-yn- 1-ols is described. The reaction is operationally straightforward and accomplished in good to excellent yiel
New easily accessible chiral indole ligands
Cozzi, Pier Giorgio,Prati, Gian Paolo,Umani-Ronchi, Achille
, p. 403 - 406 (2007/10/03)
An efficient and large-scale synthesis of indoles 3 and 4 bearing in 2-position opitically active substituents has been carried out according to the methodology introduced by Fuerstner.Furthermore, starting from indole-2-carbaldeyde, 6, the corresponding chiral indole Schiff bases 7, 8 and 9 have been synthesized.The cobalt complex, prepared from 9 and cobalt(II) acetate, has been shown to catalyze the reduction of acetophenone with NaBH4 in an e. e. of 22percent.
Pyrazine[1,2 a] and 1,4 diazepine[1,2 a]indoles. I. Synthesis of 10 phenyl 1,2,3,4 tetrahydropyrazine[1,2 a]indoles and 11 phenyl 2,3,4,5 tetrahydro 1H 1,4 diazepine[1,2 a]indoles
Gatta,Zaccari,Huidobro Toro,Landi Vittory
, p. 386 - 397 (2007/10/05)
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