Title of article :
An efficient and concise total synthesis of the antimalarial alkaloid quindoline
Author/Authors :
Bastos، نويسنده , , Dayse dos S. and Silva، نويسنده , , Anna C. and Albert، نويسنده , , André L.M. and Barros، نويسنده , , Wesley M.R. and Slana، نويسنده , , Glaucia B.C.A. and Cardoso، نويسنده , , Jari N. and Lopes، نويسنده , , Rosangela S.C. and Lopes، نويسنده , , Claudio C.، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2013
Pages :
3
From page :
3144
To page :
3146
Abstract :
The preparation of the alkaloid quindoline (1) from indol (3) through a very direct synthetic approach is described in this work. Several successive heteroaromatic lithiation reaction steps were performed in the same medium producing benzylic alcohol (7) in excellent yield. The alcohol was submitted to catalytic reduction, undergoing concomitant cyclization and aromatization, yielding quindoline (1) in 55% overall yield.
Keywords :
malaria , Quindoline , Heteroaromatic lithiation , Indoloquinolines
Journal title :
Tetrahedron Letters
Serial Year :
2013
Journal title :
Tetrahedron Letters
Record number :
1884676
Link To Document :
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