Complex Synthesis: Carbohydrates
Bibliographic References tagged with Complex Synthesis: Carbohydrates
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M.A. Sparks, K. W. Williams, C. Lukacs, A. Schrell, G. Priebe, A. Spaltenstein, and G. M. Whitesides. 1993. “Synthesis of Potential Inhibitors of Hemagglutination by Influenza Virus: Chemoenzymic Preparation of N-5 Analogs of N-Acetylneuraminic Acid”. Tetrahedron, 49, Pp. 1-12
M.A. Sparks, K. W. Williams, C. Lukacs, A. Schrell, G. Priebe, A. Spaltenstein, and G. M. Whitesides. 1993. “Synthesis of Potential Inhibitors of Hemagglutination by Influenza Virus: Chemoenzymic Preparation of N-5 Analogs of N-Acetylneuraminic Acid”. Tetrahedron, 49, Pp. 1-12
W.E. Ladner and G. M. Whitesides. 1984. “Lipase-Catalyzed Hydrolysis As a Route to Esters of Chiral Epoxy Alcohols”. J. Am. Chem. Soc., 106, Pp. 7250-51
W.E. Ladner and G. M. Whitesides. 1984. “Lipase-Catalyzed Hydrolysis As a Route to Esters of Chiral Epoxy Alcohols”. J. Am. Chem. Soc., 106, Pp. 7250-51
K. Adelhorst and G. M. Whitesides. 1993. “Large-Scale Synthesis of B-L-Fucopyranosyl Phosphate and the Preparation of GDP-B-Fucose”. Carbohyd. Res., 242, Pp. 69-76
K. Adelhorst and G. M. Whitesides. 1993. “Large-Scale Synthesis of B-L-Fucopyranosyl Phosphate and the Preparation of GDP-B-Fucose”. Carbohyd. Res., 242, Pp. 69-76
R.J. Kazlauskas and G. M. Whitesides. 1985. “Synthesis of Methoxycarbonyl Phosphate, A New Reagent Having High Phosphoryl Donor Potential for Use in ATP Cofactor Regeneration”. J. Org. Chem., 50, Pp. 1069-76
R.J. Kazlauskas and G. M. Whitesides. 1985. “Synthesis of Methoxycarbonyl Phosphate, A New Reagent Having High Phosphoryl Donor Potential for Use in ATP Cofactor Regeneration”. J. Org. Chem., 50, Pp. 1069-76
W. Schmid, L. Z. Avila, K. W. Williams, and G. M. Whitesides. 1993. “Synthesis of Methyl A-Sialosides N-Substituted With Large Alkanoyl Groups, and Investigation of Their Inhibition of Agglutination of Erythrocytes by Influenza A Virus.”. Bioorg. & Med. Chem. Lett., 3, Pp. 747-52
W. Schmid, L. Z. Avila, K. W. Williams, and G. M. Whitesides. 1993. “Synthesis of Methyl A-Sialosides N-Substituted With Large Alkanoyl Groups, and Investigation of Their Inhibition of Agglutination of Erythrocytes by Influenza A Virus.”. Bioorg. & Med. Chem. Lett., 3, Pp. 747-52
W.E. Ladner and G. M. Whitesides. 1985. “Enzymatic Synthesis of DeoxyATP Using DNA As Starting Material”. J. Org. Chem., 50, Pp. 1076-79
W.E. Ladner and G. M. Whitesides. 1985. “Enzymatic Synthesis of DeoxyATP Using DNA As Starting Material”. J. Org. Chem., 50, Pp. 1076-79
M.A. Sparks, K. W. Williams, and G. M. Whitesides. 1993. “Neuraminidase Resistant Hemagglutination Inhibitors: Acrylamide Copolymers Containing a C-Glycoside of N-Acetylneuraminic Acid”. J. Med. Chem., 36, Pp. 778-83
M.A. Sparks, K. W. Williams, and G. M. Whitesides. 1993. “Neuraminidase Resistant Hemagglutination Inhibitors: Acrylamide Copolymers Containing a C-Glycoside of N-Acetylneuraminic Acid”. J. Med. Chem., 36, Pp. 778-83
L.G. Lee and G. M. Whitesides. 1985. “Enzyme-Catalyzed Organic Synthesis: A Comparison of Strategies for in Situ Regeneration of NAD from NADH”. J. Am. Chem. Soc., 107, Pp. 6999-7008
L.G. Lee and G. M. Whitesides. 1985. “Enzyme-Catalyzed Organic Synthesis: A Comparison of Strategies for in Situ Regeneration of NAD from NADH”. J. Am. Chem. Soc., 107, Pp. 6999-7008
W. J. Lees and G. M. Whitesides. 1993. “Diastereoselectivity (Enantioselectivity) of Aldol Condensations Catalyzed by Rabbit Muscle Aldolase at C-2 of RCHOHCHO If R Has an Appropriately Placed Negatively Charged Group”. J. Org. Chem., 58, Pp. 1887-94
W. J. Lees and G. M. Whitesides. 1993. “Diastereoselectivity (Enantioselectivity) of Aldol Condensations Catalyzed by Rabbit Muscle Aldolase at C-2 of RCHOHCHO If R Has an Appropriately Placed Negatively Charged Group”. J. Org. Chem., 58, Pp. 1887-94
M. D. Bednarski, H. J. Waldmann, and G. M. Whitesides. 1986. “Aldolase-Catalyzed Synthesis of Complex C8 and C9 Monosaccharides”. Tet. Lett., Pp. 5807-10
M. D. Bednarski, H. J. Waldmann, and G. M. Whitesides. 1986. “Aldolase-Catalyzed Synthesis of Complex C8 and C9 Monosaccharides”. Tet. Lett., Pp. 5807-10