4655-89-4Relevant articles and documents
Mallotojaponins B and C: Total Synthesis, Antiparasitic Evaluation, and Preliminary SAR Studies
Grayfer, Tatyana D.,Grellier, Philippe,Mouray, Elisabeth,Dodd, Robert H.,Dubois, Jo?lle,Cariou, Kevin
supporting information, p. 708 - 711 (2016/03/01)
(Chemical Equation Presented). The first total syntheses of mallotojaponin B and C as well as several analogues have been achieved. Biological evaluation of the synthesized compounds against Plasmodium falciparum and Trypanosoma brucei have also been carried out.
Heterocycles: Part 7 - Synthesis of acetyl hydroxy-2,2-dimethylchromans
Vijayalakshmi, C. S.,Shanmugam, P.,Prasad, K. J. Rajendra
, p. 510 - 511 (2007/10/02)
Synthesis of acetyl hydroxy-2,2-dimethylchromans by two methods namely photo-Fries rearrangement of acetoxy-2,2-dimethylchromans (UV light, 253.7 nm) and Friedel-Crafts acetylation of hydroxy-2,2-dimethylchromans with gl. acetic acid using AlCl3/POCl3 has been described.
ACID-CATALYZED CONDENSATION OF ISOPRENE AND 2-METHYLBUT-3-EN-2-OL WITH PHLOROACETOPHENONE, NEW SYNTHESIS OF ALLOEVODIONOL AND FRANKLINONE
Ahluwalia, V. K.,Arora, K. K.,Jolly, R. S.
, p. 117 - 120 (2007/10/02)
The naturally occurring acetylchromenes, alloevodionol (1) and franklinone (2) have been synthesized by the nuclear isoprenylation of phloroacetophenone followed by the partial methylation and dehydrogenation of the chromans thus obtained.