Evidence for the mitochondrial biosynthesis of 3R-hydroxy-5Z,8Z,11Z,14Z-eicosatetraenoic acid in the yeastDipodascopsis uninucleata
β Scribed by Simon R. Fox; Mats Hamberg; John Friend; Colin Ratledge
- Book ID
- 107484858
- Publisher
- Springer-Verlag
- Year
- 2000
- Tongue
- English
- Weight
- 154 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0024-4201
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
An efficient and simple total synthesis of the two C(8) diastereomers of 2, of interest as possible hormonal releasing agents, is described. A previous publication from this laboratory has described the synthesis of the two diastereomeric lo-hydroxy-11, lZ(S, S)-epoxyeicosa-5,9,14(Z)-trienoic acids
Akbrt:~synthesisofdeuterhmnlsbebdll-~~acidand(ZZ)\_11,13-hexadaadienr6cacid ~~ullsetaimestigatetheb~~pPthwayofthe~essimarymothsexphcrwroneis mpaled. In .[16J6.16-\*H31 11-bex&kynoie acid, deutexium atoms wexe inlmdmxd by reaclkn of Moalkyne 6b with (CD3)@Li. Akylation of terminal diyne 14b witb CD3C