Chemo-Enzymatic Reaction Sequence for the Synthesis of Dihydroxyacetone Phosphate (DHAP) Stock Material
SK Karmee
Index: Karmee, Sanjib Kumar Synthetic Communications, 2013 , vol. 43, # 3 p. 450 - 455,6
Full Text: HTML
Citation Number: 4
Abstract
For the first time, a chemo-enzymatic synthesis of the benzylated dihydroxyacetone phosphate (DHAP) precursor starting from the glycerol is reported (Scheme 1). This method is particularly important as the free DHAP is an unstable compound whereas the benzylated dihydroxyacetone
Related Articles:
[Krief, Alain; Froidbise, Alexandre Tetrahedron, 2004 , vol. 60, # 35 p. 7637 - 7658]
A facile Er (OTf) 3-catalyzed synthesis of 2, 3-unsaturated O-and S-glycosides
[Procopio, Antonio; Dalpozzo, Renato; De Nino, Antonio; Maiuolo, Loredana; Nardi, Monica; Russo, Beatrice Advanced Synthesis and Catalysis, 2005 , vol. 347, # 10 p. 1447 - 1450]
A convenient and general iron-catalyzed hydrosilylation of aldehydes
[Shaikh, Nadim S.; Junge, Kathrin; Beller, Matthias Organic Letters, 2007 , vol. 9, # 26 p. 5429 - 5432]
Selective cleavage of ethers using silica-alumina gel catalysts prepared by the sol-gel method
[Matsumoto, Yoshihiko; Mita, Keisuke; Hashimoto, Keiji; Iio, Hideo; Tokoroyama, Takashi Tetrahedron, 1996 , vol. 52, # 28 p. 9387 - 9398]
[Malik, Satish; Kartha, K. P. Ravindranathan Synlett, 2009 , # 11 p. 1809 - 1811]