Highly Stereoselective Chemoenzymatic Synthesis of the 3 H-Isobenzofuran Skeleton. Access to Enantiopure 3-Methylphthalides
J Mangas-Sánchez, E Busto, V Gotor-Fernández…
Index: Mangas-Sanchez, Juan; Busto, Eduardo; Gotor-Fernandez, Vicente; Gotor, Vicente Organic Letters, 2012 , vol. 14, # 6 p. 1444 - 1447
Full Text: HTML
Citation Number: 17
Abstract
A straightforward synthesis of (S)-3-methylphthalides has been developed, with the key asymmetric step being the bioreduction of 2-acetylbenzonitriles. Enzymatic processes have been found to be highly dependent on the pH value, with acidic conditions being required to avoid undesired side reactions. Baker's yeast was found to be the best biocatalyst acting in a highly stereoselective fashion. The simple treatment of the reaction crudes with aqueous ...
Related Articles:
Design of new reaction conditions for the Sugasawa reaction based on mechanistic insights
[Tabuchi, Seiichiro; Ito, Harunobu; Sogabe, Hajime; Kuno, Masako; Kinoshita, Takayoshi; Katumi, Ikuyo; Yamamoto, Naoko; Mitsui, Hitoshi; Satoh, Yoshinari Chemical and Pharmaceutical Bulletin, 2000 , vol. 48, # 1 p. 1 - 15]
Surface photochemistry: the amide Photo-Fries rearrangement
[Magdy, M.; Malik, Abdel-; Mayo, Paul de Canadian Journal of Chemistry, 1984 , vol. 62, p. 1275 - 1278]