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- Erythrose revealed as furanose forms. Carlos Cabezas, Isabel Peña, Adam M. Daly, José L. Alonso
, Chem. Commun.
, 2013
, 49
, 10826
- Aspects of stereochemistry. Part XXIV. The acid-catalysed rearrangement of 2,4-O-benzylidene-D-erythrose and 2,3-O-benzylidene-erythritol. N. Baggett, K. W. Buck, A. B. Foster, B. H. Rees, J. M. Webber
, J. Chem. Soc. C
, 1966
, 212
- 288. Deoxy-sugars. Part IV. A synthesis of 2-deoxy-D-ribose from D-erythrose. W. G. Overend, M. Stacey, L. F. Wiggins
, J. Chem. Soc.
, 1949
, 1358
- StnK2 catalysing a Pictet–Spengler reaction involved in the biosynthesis of the antitumor reagent streptonigrin. Xiaozheng Wang, Dekun Kong, Tingting Huang, Zixin Deng, Shuangjun Lin
, Org. Biomol. Chem.
, 2018
, 16
, 9124
- Non-stoichiometric formation of formic and levulinic acids from the hydrolysis of biomass derived hexose carbohydrates. T. Flannelly, M. Lopes, L. Kupiainen, S. Dooley, J. J. Leahy
, RSC Adv.
, 2016
, 6
, 5797
- Synthesis of (d)-erythrose from glycolaldehyde aqueous solutions under electric field. Giuseppe Cassone, Jiri Sponer, Judit E. Sponer, Fabio Pietrucci, A. Marco Saitta, Franz Saija
, Chem. Commun.
, 2018
, 54
, 3211
- Synthesis of pyrrolidine homoazasugars and 3,4-dihydroxy-5-hydroxymethylprolines using aldol additions of metalated bislactim ethers to 2,4-O-ethylidene-d-erythroses. Olga Blanco, Cristina Pato, María Ruiz, Vicente Ojea
, Org. Biomol. Chem.
, 2009
, 7
, 2310
- Successive C1–C2 bond cleavage: the mechanism of vanadium(v)-catalyzed aerobic oxidation of d-glucose to formic acid in aqueous solution. Muge Niu, Yucui Hou, Weize Wu, Shuhang Ren, Ru Yang
, Phys. Chem. Chem. Phys.
, 2018
, 20
, 17942
- Development of small peptides recognizing a
monosaccharide by combinatorial chemistry. Naoki Sugimoto, Daisuke Miyoshi, Jin Zou
, Chem. Commun.
, 2000
, 2295
- (3S,4R)-3,4-Dihydroxy-N-alkyl-l-homoprolines: synthesis and computational mechanistic studies. David S. Freitas, Cristina E. A. Sousa, Joana Parente, Artem Drogalin, António Gil Fortes, Nuno M. F. S. A. Cerqueira, Maria J. Alves
, Org. Biomol. Chem.
, 2019
, 17
, 10052