Brun, Elodie published the artcileDiastereo- and enantioselective synthesis of 1,3,5,7-tetraol structural units using a Prins cyclisation-reductive cleavage sequence, Synthetic Route of 57044-25-4, the publication is Chemical Communications (Cambridge, United Kingdom) (2014), 50(51), 6718-6721, database is CAplus and MEDLINE.
Stereocontrolled and efficient access to all the diastereomers of 1,3,5,7-tetraol structural units I was developed using a Prins cyclization-reductive cleavage sequence applied to tetrahydropyran aldehydes II. Furthermore, these tetraols can be selectively functionalized.
Chemical Communications (Cambridge, United Kingdom) published new progress about 57044-25-4. 57044-25-4 belongs to alcohols-buliding-blocks, auxiliary class Epoxides,Chiral,Aliphatic hydrocarbon chain,Alcohol, name is (R)-Oxiran-2-ylmethanol, and the molecular formula is C3H6O2, Synthetic Route of 57044-25-4.
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