Ohtsuka, Eiko published the artcileStudies on transfer ribonucleic acids and related compounds. XLIV. A large-scale synthesis of the anticodon heptanucleotide of formyl-methionine transfer ribonucleic acid by using 2′-O-tetrahydrofuranylnucleosides, Recommanded Product: N-(9-((6aR,8R,9R,9aS)-9-Hydroxy-2,2,4,4-tetraisopropyltetrahydro-6H-furo[3,2-f][1,3,5,2,4]trioxadisilocin-8-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)isobutyramide, the publication is Chemical & Pharmaceutical Bulletin (1983), 31(6), 1910-16, database is CAplus and MEDLINE.
2′-O-Tetrahydrofuranyl nucleosides were prepared by an improved procedure via 3′,5′-tetraisopropyldisiloxanyl nucleosides. A large-scale synthesis of the anticodon heptanucleotide C-U-C-A-U-A-A of Escherichia coli formylmethionine tRNA was performed by the phosphotriester method involving condensation of oligonucleotides having 2′-O-tetrahydrofuranyl protecting groups.
Chemical & Pharmaceutical Bulletin published new progress about 87865-78-9. 87865-78-9 belongs to tetrahydrofurans, auxiliary class Nucleosides and Nucleotides,Nucleoside Analogues, name is N-(9-((6aR,8R,9R,9aS)-9-Hydroxy-2,2,4,4-tetraisopropyltetrahydro-6H-furo[3,2-f][1,3,5,2,4]trioxadisilocin-8-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)isobutyramide, and the molecular formula is C26H45N5O7Si2, Recommanded Product: N-(9-((6aR,8R,9R,9aS)-9-Hydroxy-2,2,4,4-tetraisopropyltetrahydro-6H-furo[3,2-f][1,3,5,2,4]trioxadisilocin-8-yl)-6-oxo-6,9-dihydro-1H-purin-2-yl)isobutyramide.
Referemce:
https://en.wikipedia.org/wiki/Tetrahydrofuran,
Tetrahydrofuran | (CH2)3CH2O – PubChem