205308-02-7Relevant articles and documents
1,5-Diphenylpenta-2,4-dien-1-ones as potent and selective monoamine oxidase-B inhibitors
Desideri, Nicoletta,Fioravanti, Rossella,Proietti Monaco, Luca,Biava, Mariangela,Yanez, Matilde,Ortuso, Francesco,Alcaro, Stefano
, p. 91 - 100 (2013/03/13)
A series of (2E,4E)-1-(2-hydroxyphenyl)-5-phenylpenta-2,4-dien-1-ones (3a-r) and (2Z,4E)-3-hydroxy-1-(2-hydroxyphenyl)-5-phenylpenta-2,4-dien-1-ones (6a-l) were synthesized and evaluated in vitro as inhibitors of the two human Monoamine oxidase (hMAO) iso
A novel and efficient route for the synthesis of hydroxylated 2,3-diarylxanthones
Santos, Clementina M. M.,Silva, Artur M. S.,Cavaleiro, José A. S.
, p. 3113 - 3116 (2008/09/19)
A novel, efficient and general route for the synthesis of hydroxylated 2,3-diarylxanthones is described. 3-Bromo-2-styryl-chromone, the key intermediate of this synthesis, is obtained by a Baker-Venkataraman rearrangement of the appropriate 2′-cinnamoylox
The synthesis of various cycloalkana[d]xanthones and conversion of the cyclohexa-analogue to a 7,7a-dimethylcyclohexa-[d]xanthene
Letcher, Roy M.,Yue, Tai-Yuen,Chiu, Kwei-Fung,Kelkar, Avijit S.,Cheung, Kung-Kai
, p. 3267 - 3276 (2007/10/03)
The synthesis of cyclo-penta-, -hexa- and -hepta-[d]xanthones 5 from (E)-(2-hydroxyphenyl)-5-arylpent-4-ene-1,3-diones 4, cycloalkanones and pyrrolidine is described. Reactions to modify 5 in an attempt to synthesize analogues of the five naturally occurr
