55094-52-5
55094-52-5
Chemical Structure
2,3,5-Tri-O-benzyl-D-ribono-1,4-lactone
- CAS No.: 55094-52-5
- Formula:C26H26O5
- Molecular Weight:418.49
IUPAC Name: (3R,4R,5R)-3,4-bis(benzyloxy)-5-((benzyloxy)methyl)dihydrofuran-2(3H)-one
InChIKey: LDHBSABBBAUMCZ-UBFVSLLYSA-N
SMILES: O=C1O[C@H](COCC2=CC=CC=C2)[C@@H](OCC3=CC=CC=C3)[C@H]1OCC4=CC=CC=C4
Biological Activity: 2,3,5-Tri-O-benzyl-D-ribono-1,4-lactone is a nucleoside analog[1][2][3][4].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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2,3,5-Tri-O-benzyl-D-ribono-1,4-lactone | 99.97% | 2,3,5-Tri-O-benzyl-D-ribono-1,4-lactone is a nucleoside analog. | ||||||||||||||||||||
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References
- [1]. Minasov G, et al. Crystal structure of an RNA duplex containing phenyl-ribonucleotides, hydrophobic isosteres of the natural pyrimidines. RNA (New York, N.Y.). 2000 Nov;6(11):1516-28.
- [2]. van Rijssel ER, et al. Stereoselectivity in the Lewis acid mediated reduction of ketofuranoses. The Journal of organic chemistry. 2015 May 01;80(9):4553-65.
- [3]. Lambu MR, et al. Synthesis of C-spiro-glycoconjugates from sugar lactones via zinc mediated Barbier reaction. RSC Adv. 2014;4(22):11023-11028.
- [4]. Najczuk JJ, et al. Light-Driven Regioselective Deoxygenation of Carbohydrate Lactones for 2-Deoxy Sugar Precursor Synthesis. Organic letters. 2025 Feb 07;27(5):1221-1225.
