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3.11- Dihydroxymyristic acid

Convolvulinolic acid = (115)-hydroxytetradecanoic acid = 11-hydroxymyristic acid Ipolearic acid = (35,115)-dihydroxyhexadecanoic acid = 3,11-dihydroxypalmitic acid Ipurolic acid = (35,11 -dihydroxytetradecanoic acid = 3,11-dihydroxymyristic acid Jalapinolic acid = (115)-(+)-hydroxyhexadecanoic acid = 11-hydroxypalmitic acid Operculinolic acid = 3,12-dihydroxyhexadecanoic acid = 3,12-dihydroxypalmitic acid Turpetholic acid A = 3,12-dihydroxypentadecanoic acid Turpetholic acid B = 4,12-dihydroxypentadecanoic acid... [Pg.533]

The (S)-enantiomer was predominantly hydroxylated to the diastereoisomer three-12,13-dihydroxymyristic acid (80% (12J ,13R)-12,13-dihydroxymyristic add and 20% (12J ,13S)-12,13-dihydroxymyristic acid). When (i )-13-hydroxymyristic acid was used as substrate in a similar reaction system, mainly erythro-12,13-dihydroxymyrisitic add (85% (12S,13i )-12,13-dihydroxymyristic add and 15% (12R,13J )-12,13-dihydroxymyristic acid) was generated (Scheme 5.19) [82]. [Pg.109]

Scheme 5.19 Regio- and stereoselective dihydroxymyristic acid synthesis using P450 BM3. Scheme 5.19 Regio- and stereoselective dihydroxymyristic acid synthesis using P450 BM3.
See other pages where 3.11- Dihydroxymyristic acid is mentioned: [Pg.558]    [Pg.559]    [Pg.840]    [Pg.556]    [Pg.558]    [Pg.559]    [Pg.840]    [Pg.556]    [Pg.108]    [Pg.109]    [Pg.109]    [Pg.109]    [Pg.109]    [Pg.109]   
See also in sourсe #XX -- [ Pg.13 , Pg.312 ]

See also in sourсe #XX -- [ Pg.13 , Pg.312 ]



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