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- Aluminium triflate catalysed O-glycosidation: temperature-switched selective Ferrier rearrangement or direct addition with alcohols. D. Bradley G. Williams, Sandile B. Simelane, Henok H. Kinfe
, Org. Biomol. Chem.
, 2012
, 10
, 5636
- C-2 auxiliaries for stereoselective glycosylation based on common additive functional groups. Frank F. J. de Kleijne, Sam J. Moons, Paul B. White, Thomas J. Boltje
, Org. Biomol. Chem.
, 2020
, 18
, 1165
- Facile O-glycosylation of glycals using Glu-Fe3O4-SO3H, a magnetic solid acid catalyst. Raju S. Thombal, Vrushali H. Jadhav
, RSC Adv.
, 2016
, 6
, 30846
- Lewis acid–surfactant-combined catalyzed synthesis of 4-aminocyclopentenones from glycals in water. Siming Wang, Ronny William, Kim Kui Georgina Estelle Seah, Xue-Wei Liu
, Green Chem.
, 2013
, 15
, 3180
- ‘Chiron’ approach to stereoselective synthesis of sphinganine and unnatural safingol, an antineoplastic and antipsoriatic agent. Pintu Das, Somireddy Kundooru, Arun K. Shaw
, RSC Adv.
, 2016
, 6
, 14505
- A concise synthesis of 3-deoxy-2-O-methyl-4,5,7-tri-O-benzyl-D-arabino-heptulosonic acid and related compounds from 3,4,6-tri-O-benzyl-D-glucal. David Crich, Timothy J. Ritchie
, J. Chem. Soc., Chem. Commun.
, 1988
, 985
- Cationic poly-amido-saccharides: stereochemically-defined, enantiopure polymers from anionic ring-opening polymerization of an amino-sugar monomer. Anant S. Balijepalli, Aladin Hamoud, Mark W. Grinstaff
, Polym. Chem.
, 2020
, 11
, 1926
- The evolution of comprehensive strategies for furanoid glycal synthesis and their applications. Pinki Pal, Arun K. Shaw
, RSC Adv.
, 2017
, 7
, 25897
- Substrate and stereocontrolled iodocycloetherification of highly functionalized enantiomerically pure allylic alcohols: application to synthesis of cytotoxic 2-epi jaspine B and its biological evaluation. Somireddy Kundooru, Pintu Das, Sanjeev Meena, Vikash Kumar, Mohammad Imran Siddiqi, Dipak Datta, Arun K. Shaw
, Org. Biomol. Chem.
, 2015
, 13
, 8241
- Stereodivergent routes in organic synthesis: carbohydrates, amino acids, alkaloids and terpenes. Carmen Nájera, Francisco Foubelo, José M. Sansano, Miguel Yus
, Org. Biomol. Chem.
, 2020
, 18
, 1232