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| 3,5-Di-O-(tert-butyldimethylsilyl)-2-deoxy-D-ribonolactone Basic information |
Product Name: | 3,5-Di-O-(tert-butyldimethylsilyl)-2-deoxy-D-ribonolactone | Synonyms: | D-erythro-Pentonicacid, 2-deoxy-3,5-bis-O-[(1,1-dimethylethyl)dimethylsilyl]-, g-lactone;(4S,5R)‐4‐[(tert‐butyldimethylsilyl)oxy]‐5‐{[(tert‐butyldimethylsilyl)oxy]methyl}oxolan‐2‐one;3,5-DI-O-(T-BUTYLDIMETHYLSILYL)-2-DEOXY-D-RIBONOLACTONE;(3S,4R)-3,5-bis(tert-butyldimethylsilyloxy)-4-hydroxypentanal;3,5-Di-O-(t-Butyldimethylsilyl)-2-deoxy-D-ribono-1,4-lactone;3,5-Di-O-(tert-butyldimethylsilyl)-2-deoxy-D-ribose;3,5-Di-O-(tert-butyldimethylsilyl)-2-deoxy-D-ribono-1,4-lactone;3,5-DI-O-(TERT-BUTYLDIMETHYLSILYL)-2-DEOXY-D-RIBONOLACTONE | CAS: | 83159-91-5 | MF: | C17H36O4Si2 | MW: | 360.64 | EINECS: | | Product Categories: | | Mol File: | 83159-91-5.mol | |
| 3,5-Di-O-(tert-butyldimethylsilyl)-2-deoxy-D-ribonolactone Chemical Properties |
| 3,5-Di-O-(tert-butyldimethylsilyl)-2-deoxy-D-ribonolactone Usage And Synthesis |
Uses | (4S,5R)-4-(tert-Butyldimethylsilyloxy)-5-((tert-butyldimethylsilyloxy)methyl)dihydrofuran-2(3H)-one is used as a reactant in the synthesis of 6-substituted pyridin-3-yl C-nucleosides using Heck arylation, palladium-catalyzed cross-coupling, amination, and alkoxylation reactions. |
| 3,5-Di-O-(tert-butyldimethylsilyl)-2-deoxy-D-ribonolactone Preparation Products And Raw materials |
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