Induction of a Preferred Sense of Twist in Flexible Diphenyls by Carbohydrate Scaffolds. Synthesis of Two “Naked” Ellagitannin Analogous was written by Capozzi, Giuseppe;Ciampi, Cinzia;Delogu, Giovanna;Menichetti, Stefano;Nativi, Cristina. And the article was included in Journal of Organic Chemistry in 2001.Synthetic Route of C6H14O6 This article mentions the following:
The synthesis of “naked ” ellagitannin analogs, having a preferred sense of twist of the di-Ph moiety, with a rhamnose and a glucose template, is reported. A clear induction in the chirality of the di-Ph moiety, mediated through a 10-membered ring via ester linkages, was observed The chiral scaffold of glucose (diequatorial 2,3-hydroxyl groups) exerts a remarkable stronger atropdiastereoselective effect onto the diphenoyl group than the rhamnose ring (axial-equatorial 2,3-hydroxyl groups), according to the Schmidt-Haslam hypothesis. In the experiment, the researchers used many compounds, for example, (2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal hydrate (cas: 10030-85-0Synthetic Route of C6H14O6).
(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal hydrate (cas: 10030-85-0) belongs to alcohols. Alcohols are among the most common organic compounds. They are used as sweeteners and in making perfumes, are valuable intermediates in the synthesis of other compounds, and are among the most abundantly produced organic chemicals in industry. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.Synthetic Route of C6H14O6
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts