181356-76-3Relevant academic research and scientific papers
Ring-closing metathesis for the synthesis of 2H- and 4H-chromenes
Van Otterlo, Willem A.L.,Ngidi, E. Lindani,Kuzvidza, Samuel,Morgans, Garreth L.,Moleele, Simon S.,De Koning, Charles B.
, p. 9996 - 10006 (2007/10/03)
Six 4H-chromenes were synthesized from substituted phenols using vinylstannylation and ring-closing metathesis (RCM) as key steps. In addition, a different approach involving amongst other steps, an aryl allyl isomerization and RCM afforded a set of seven 2H-chromenes from phenolic precursors.
Ring-closing metathesis for the synthesis of benzo-fused bicyclic compounds
Van Otterlo, Willem A.L.,Ngidi, E. Lindani,Coyanis, E. Mabel,De Koning, Charles B.
, p. 311 - 313 (2007/10/03)
Ring-closing metathesis (RCM) was used to synthesise five 4H-chromenes, a naphthol and an indenol. These are the first examples of RCM applied to the synthesis of such benzo-fused bicyclic compounds.
Convenient Synthesis of 1-Butyl-2,3,5-trioxygenated Benzenes: Synthesis of the Di-O-methyl Ether of the Aglycone of Cesternoside A
Mali, Raghao S.,Garkhedkar, Milind P.,Sindkhedkar, Milind D.,Dhavale, Dilip D.
, p. 342 - 343 (2007/10/03)
The synthesis of the di-O-methyl ether of the aglycone of cesternoside A (3 = 10a), 2-iso-butyl-4,6-dimethoxyphenol (10b) and 2-sec- and 2-iso-butyl-4-methoxyphenols (10c and 10d) is described from the corresponding phenols (7a and 7b) via the intermediac
