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- One-pot, two-step cascade synthesis of naturally rare l-erythro (3S,4S) ketoses by coupling a thermostable transaminase and transketolase. Marion Lorillière, Maxime De Sousa, Felipe Bruna, Egon Heuson, Thierry Gefflaut, Véronique de Berardinis, Thangavelu Saravanan, Dong Yi, Wolf-Dieter Fessner, Franck Charmantray, Laurence Hecquet
, Green Chem.
, 2017
, 19
, 425
- Catalytic enantioselective aldol reactions. Yasuhiro Yamashita, Tomohiro Yasukawa, Woo-Jin Yoo, Taku Kitanosono, Shū Kobayashi
, Chem. Soc. Rev.
, 2018
, 47
, 4388
- Efficient biocatalytic processes for highly valuable terminally phosphorylated C5 to C9 d-ketoses. C. Guérard-Hélaine, M. Debacker, P. Clapés, A. Szekrenyi, V. Hélaine, M. Lemaire
, Green Chem.
, 2014
, 16
, 1109
- Broadening the reaction scope of unprotected aldoses via their corresponding nitrones: 1,3-dipolar cycloadditions with alkenes. Gatien Messire, Fabien Massicot, Laura Pascual, Emmanuel Riguet, Jean-Luc Vasse, Jean-Bernard Behr
, Org. Biomol. Chem.
, 2020
, 18
, 5708
- The preparation of aldotetroses from aldopentoses via 1 : 1-diethylsulphonyl-3 : 4 : 5-trihydroxypent-1-enes. L. Hough, T. J. Taylor
, J. Chem. Soc.
, 1955
, 1212
- 630. Four-carbon saccharinic acids from the alkaline degradation of 3-O-methyl-L-glycerotetrulose and 4-O-methyl-D-threose. G. N. Richards
, J. Chem. Soc.
, 1957
, 3222
- Efficient asymmetric organocatalytic formation of erythrose and threose under aqueous conditions. Laurence Burroughs, Matthew E. Vale, James A. R. Gilks, Henrietta Forintos, Christopher J. Hayes, Paul A. Clarke
, Chem. Commun.
, 2010
, 46
, 4776
- The formation, under kinetic control, of a new monoacetal (2,3-O-butylidene-D-glucitol) from D-glucitol and n-butyraldehyde. T. G. Bonner, E. J. Bourne, P. J. V. Cleare, D. Lewis
, J. Chem. Soc. B
, 1968
, 822
- 312. The synthesis of sugars from simpler substances. Part VI. Enzymic synthesis of D-idoheptulose. P. A. J. Gorin, J. K. N. Jones
, J. Chem. Soc.
, 1953
, 1537
- Asymmetric organocatalytic formation of protected and unprotected tetroses under potentially prebiotic conditions. Laurence Burroughs, Paul A. Clarke, Henrietta Forintos, James A. R. Gilks, Christopher J. Hayes, Matthew E. Vale, William Wade, Myriam Zbytniewski
, Org. Biomol. Chem.
, 2012
, 10
, 1565