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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
- 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
- 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
- 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
- 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
- Synthesis and antiviral evaluation of base-modified deoxythreosyl nucleoside phosphonates. Chao Liu, Shrinivas G. Dumbre, Christophe Pannecouque, Brent Korba, Steven De Jonghe, Piet Herdewijn
, Org. Biomol. Chem.
, 2017
, 15
, 5513
- 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
- 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