Identification and Optimization of an Aminoalcohol-Carbazole Series with Antimalarial Properties

Jérôme Molette; Julie Routier; Nada Abla; Dominique Besson; Agnes Bombrun; Reto Brun; Howard Burt; Katrin Georgi; Marcel Kaiser; Solomon Nwaka; Mathilde Muzerelle; Alexander Scheer

doi:10.1021/ml400015f

Identification and Optimization of an Aminoalcohol-Carbazole Series with Antimalarial Properties

ACS Medicinal Chemistry Letters ◽

10.1021/ml400015f ◽

2013 ◽

Vol 4 (11) ◽

pp. 1037-1041 ◽

Cited By ~ 21

Author(s):

Jérôme Molette ◽

Julie Routier ◽

Nada Abla ◽

Dominique Besson ◽

Agnes Bombrun ◽

...

Keyword(s):

Carbazole Series

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ChemInform Abstract: SELECTIVE PHOTO-BROMINATION IN THE CARBAZOLE SERIES, A STUDY

Chemischer Informationsdienst ◽

10.1002/chin.197450249 ◽

1974 ◽

Vol 5 (50) ◽

pp. no-no

Author(s):

M. T. GOETZ

Keyword(s):

Carbazole Series

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CCCXXV.—The diazo-reaction in the carbazole series. Carbazole-3-diazoimine and -3-diazonium salts

Journal of the Chemical Society Transactions ◽

10.1039/ct9222102709 ◽

1922 ◽

Vol 121 (0) ◽

pp. 2709-2717 ◽

Cited By ~ 5

Author(s):

Gilbert T. Morgan ◽

Hugh Norman Read

Keyword(s):

Diazonium Salts ◽

Carbazole Series

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Antimonial analogues of the carbazole serier

Proceedings of the Royal Society of London. Series A, Containing Papers of a Mathematical and Physical Character ◽

10.1098/rspa.1930.0040 ◽

1930 ◽

Vol 127 (804) ◽

pp. 1-8 ◽

Cited By ~ 9

Keyword(s):

Organic Chemistry ◽

Carbazole Series ◽

Hydrocarbon Radicals

Although arsenic and antimony exhibit certain similarities in regard to their combinations with hydrocarbon radicals yet the organic chemistry of the latter metalloid is still in a much more fragmentary condition than that of the former element because of the greater experimental difficulties which attend the preparation of organic antimonials. These difficulties are two-fold : the first is the ease with which antimony is dislodged from its attachment to carbon, the second arises from the amorphous and colloidal nature of organic stibinic acids. In a former communication* we discussed the antimonial analogues of the cacodyl series whereas in the present one we describe certain organic derivatives in which antimony replaces nitrogen in the carbazole nucleus, these compounds being analogues of the arsenical carbazole series already studied by Aeschlimann, Lees, McClelland and Nicklin.

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