A practical access to glucose-and allose-based (5+ 5) 3-spiropseudonucleosides from a common intermediate
…, V Rodins, E Rolava, P Ostrovskis, S Belyakov
Index: Turks, Maris; Rodins, Vitalijs; Rolava, Evija; Ostrovskis, Pavels; Belyakov, Sergey Carbohydrate Research, 2013 , vol. 375, p. 5 - 15
Full Text: HTML
Citation Number: 17
Abstract
A practical access to glucose-based and allose-based spirooxazolidinones is reported. The synthetic sequence consisting of TEMPO-catalyzed oxidation of 1, 2: 5, 6-di-O- isopropylidene-α-d-glucofuranose, Henry reaction, and reduction provides amino alcohol with allo-configuration on a multigram scale. Alternatively, water elimination from Henry products followed by a rehydration gives an access to diastereomerically pure glucose- ...
Related Articles:
[Silva, Sandrina; Sanchez-Fernandez, Elena M.; Ortiz Mellet, Carmen; Tatibouet, Arnaud; Pilar Rauter, Amelia; Rollin, Patrick European Journal of Organic Chemistry, 2013 , # 35 p. 7941 - 7951]
[Hoffmann-Roeder, Anja; Johannes, Manuel Chemical Communications, 2011 , vol. 47, # 35 p. 9903 - 9905]
[Chandrasekhar; Mohanty, Pradyumna K.; Ramachander Synlett, 1999 , # 7 p. 1063 - 1064]
Sugar furanoid trans-vicinal diacid as a γ-turn inducer: synthesis and conformational study
[Vangala, Madhuri; Dhokale, Snehal A.; Gawade, Rupesh L.; Pattuparambil, Rajamohanan R.; Puranik, Vedavati G.; Dhavale, Dilip D. Organic and Biomolecular Chemistry, 2013 , vol. 11, # 40 p. 6874 - 6878]
[Hall, Adrian; Bailey, Patrick D.; Rees, David C.; Rosair, Georgina M.; Wightman, Richard H. Journal of the Chemical Society, Perkin Transactions 1, 2000 , # 3 p. 329 - 343]