943896-07-9Relevant articles and documents
Enantioselective Total Syntheses of (+)-Hostmanin A, (-)-Linderol A, (+)-Methyllinderatin and Structural Reassignment of Adunctin E
Dethe, Dattatraya H.,Dherange, Balu D.
, p. 4526 - 4531 (2015)
A one-step protocol has been developed for the enantioselective synthesis of hexahydrodibenzofuran derivatives using a modified Friedel-Crafts reaction. The developed method was applied to the synthesis of a series of natural products including (+)-hostmanin A, (+)-methyllinderatin, and (-)-linderol A. The synthetic and spectroscopic data investigations led to the structural reassignment of natural product adunctin E, which was further confirmed by single-crystal X-ray analysis. (Chemical Presented).
The first total syntheses of (+)-hostmanin a and (+)-methyllinderatin
Kitao, Junko,Kitamura, Naoko,Kumo, Nozomi,Arimitsu, Kenji,Iwasaki, Hiroki,Ozeki, Minoru,Kurume, Ai,Yamashita, Masayuki
experimental part, p. 143 - 151 (2011/04/21)
The first total syntheses of (+)-hostmanin A (1) and (+)-methyllinderatin (3) were achieved in four steps from a known compound, 1-{2, 6-dihydroxy-4-methoxy-3-[(1R, 6R)-3-methyl-6-(1-methylethyl)-2-cyclohexen-1-yl] phenyl}ethanone (6). The absolute config