1821-20-1Relevant articles and documents
A Rh(iii)-catalyzed cascade C-H functionalization/cyclization reaction of salicylaldehydes with diazomalonates for the synthesis of 4-hydroxycoumarin derivatives
Xu, Guo-Dong,Huang, Zhi-Zhen
supporting information, p. 18358 - 18362 (2018/11/21)
A cascade C-H functionalization/cyclization reaction of salicylaldehydes with α-diazomalonates has been developed for the synthesis of 4-hydroxycoumarin derivatives under the catalysis of rhodium(iii) and in the presence of acetic acid. A plausible mechanism involving aldehydic C(sp2)-H activation by rhodium(iii) and rhodium(iii) catalyzed carbene insertion is also proposed.
Synthesis and evaluation of the antioxidant and anti-inflammatory activity of novel coumarin-3-aminoamides and their alpha-lipoic acid adducts
Melagraki, Georgia,Afantitis, Antreas,Igglessi-Markopoulou, Olga,Detsi, Anastasia,Koufaki, Maria,Kontogiorgis, Christos,Hadjipavlou-Litina, Dimitra J.
scheme or table, p. 3020 - 3026 (2009/10/02)
In the present work a series of novel coumarin-3-carboxamides and their hybrids with the alpha-lipoic acid were designed, synthesized and tested as potent antioxidant and anti-inflammatory agents. The new compounds were evaluated for their antioxidant act
Ring Closure and Rearrangement Reactions of 4-Azido-2-oxoquinoline-3-carboxylates and 4-Azidocoumarin-3-carboxylates [1]
Stadlbauer, Wolfgang,Prattes, Susanne,Fiala, Werner
, p. 627 - 636 (2007/10/03)
4-Azido-2-oxoquinoline-3-carboxylates and 4-azidocoumarin-3-carboxylates 6, which were obtained from the corresponding 4-hydroxy derivatives 1 via 4-tosylates 2 or 4-chloro compounds 4, cyclized upon thermolysis to 3-alkoxyisoxazolo[4,3-c]quinolin-4(5H)-ones or the corresponding coumarins 8, whereas at slightly higher temperatures a 3-O, 4-O-rearrangement took place to give the 4-alkoxy-isoxazolo[4,3-c]-quinolin-3-ones and the corresponding coumarins 9. The necessary reaction conditions could be obtained easily with the help of differential scanning calorimetry.