Synthetic microbial chemistry. X. Synthesis of the natural enantiomers of ascochlorin, ascofuranone and ascofuranol was written by Mori, Kenji;Takechi, Shozo. And the article was included in Tetrahedron in 1985.HPLC of Formula: 37905-02-5 The following contents are mentioned in the article:
The title compounds I–III were prepared together with (+)-ascofurarone and (+)-ascofuranol. The absolute configuration of (-)-ascofuranol (III) was confirmed to be 1”S,4”S. This study involved multiple reactions and reactants, such as (2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5HPLC of Formula: 37905-02-5).
(2E,6E)-3,7-Dimethyl-8-oxoocta-2,6-dien-1-yl acetate (cas: 37905-02-5) belongs to esters. Volatile esters with characteristic odours are used in synthetic flavours, perfumes, and cosmetics. Certain volatile esters are used as solvents for lacquers, paints, and varnishes. Esters are more polar than ethers but less polar than alcohols. They participate in hydrogen bonds as hydrogen-bond acceptors, but cannot act as hydrogen-bond donors, unlike their parent alcohols. This ability to participate in hydrogen bonding confers some water-solubility.HPLC of Formula: 37905-02-5
Referemce:
Ester – Wikipedia,
Ester – an overview | ScienceDirect Topics