-
1
-
-
83455163266
-
-
ed. B. O. F. Reid, K. Tatsuta and J. Thiem, Springer-Verlag, Berlin, Heiderberg, New York
-
O. Blixt and N. Razi, in Glycoscience, 2nd edn, ed., B. O. F. Reid, K. Tatsuta, and, J. Thiem, Springer-Verlag, Berlin, Heiderberg, New York, 2008, Vol. 2, pp. 1361-1385
-
(2008)
Glycoscience, 2nd Edn
, vol.2
, pp. 1361-1385
-
-
Blixt, O.1
Razi, N.2
-
8
-
-
0001423011
-
-
ed. S. H. Khan and R. A. O'Neill, Harwood Academic Publishers
-
K. G. I. Nilsson, in Modern Methods in Carbohydrate Synthesis, ed., S. H. Khan, and, R. A. O'Neill, Harwood Academic Publishers, 1996, pp. 518-547
-
(1996)
Modern Methods in Carbohydrate Synthesis
, pp. 518-547
-
-
Nilsson, K.G.I.1
-
9
-
-
84961309849
-
-
ed. B. Ernst, G. W. Hart and P. Sinaÿ, Wiley-VCH, Weinheim
-
D. J. Vocadlo and S. G. Withers, in Carbohydrates in Chemistry and Biology, ed., B. Ernst, G. W. Hart, and, P. Sinaÿ, Wiley-VCH, Weinheim, 2000, Vol 2, pp. 723-844
-
(2000)
Carbohydrates in Chemistry and Biology
, vol.2
, pp. 723-844
-
-
Vocadlo, D.J.1
Withers, S.G.2
-
10
-
-
1442315217
-
-
B. O. Fraser-Reid, K. Tatsuta and J. Thiem, Springer-Verlag, Berlin, Heidelberg, New York
-
S. Shoda, in Glycoscience, ed., B. O. Fraser-Reid, K. Tatsuta, and, J. Thiem, Springer-Verlag, Berlin, Heidelberg, New York, 2001, Vol. II, pp. 1465-1496
-
(2001)
Glycoscience
, vol.2
, pp. 1465-1496
-
-
Shoda, S.1
-
11
-
-
78649903099
-
-
J. P. Kamerling, Elsevier, Oxford
-
P. Bojarová-Fialová and V. Ken, in Comprehensive Glycoscience, ed., J. P. Kamerling, 2007, Elsevier, Oxford, 2007, Vol. 1, pp. 453-487
-
(2007)
Comprehensive Glycoscience
, vol.1
, pp. 453-487
-
-
Bojarová-Fialová, P.1
Ken, V.2
-
12
-
-
64249123668
-
-
ed. B. O. Fraser-Reid, K. Tatsuta and J. Thiem Springer-Verlag, Berlin, Heidelberg, New York
-
J. Thiem, in Glycoscience, ed., B. O. Fraser-Reid, K. Tatsuta, and J. Thiem, Springer-Verlag, Berlin, Heidelberg, New York, 2008, Vol. II, pp. 1387-1409
-
(2008)
Glycoscience
, vol.2
, pp. 1387-1409
-
-
Thiem, J.1
-
19
-
-
0036935764
-
-
S. Shoda M. Fujita C. Lohavisavapanichi Y. Misawa K. Ushizaki Y. Tawata M. Kuriyama M. Kohri H. Kuwata T. Watanabe Helv. Chim. Acta 2002 85 3919 3936
-
(2002)
Helv. Chim. Acta
, vol.85
, pp. 3919-3936
-
-
Shoda, S.1
Fujita, M.2
Lohavisavapanichi, C.3
Misawa, Y.4
Ushizaki, K.5
Tawata, Y.6
Kuriyama, M.7
Kohri, M.8
Kuwata, H.9
Watanabe, T.10
-
34
-
-
28844453238
-
-
Z. J. Kamiński B. Kolesińska J. Kolesińska G. Sabatino M. Cheli P. Rovero M. Błaszczyk M. L. Główka A. M. Papini J. Am. Chem. Soc. 2005 127 16912 16920
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 16912-16920
-
-
Kamiński, Z.J.1
Kolesińska, B.2
Kolesińska, J.3
Sabatino, G.4
Cheli, M.5
Rovero, P.6
Błaszczyk, M.7
Główka, M.L.8
Papini, A.M.9
-
35
-
-
78049321357
-
-
Use of other bases, 2,6-lutidine or triethylamine, resulted in a decrease of the yield
-
Use of other bases, 2,6-lutidine or triethylamine, resulted in a decrease of the yield.
-
-
-
-
37
-
-
78049339503
-
-
WO 2000053544
-
F. Iwasaki, M. Miharu, N. Hirano, M. Saijyo, S. Tani, M. Kunishima and K. Terao, PCT Int. Appl., WO 2000053544, 2000
-
(2000)
PCT Int. Appl.
-
-
Iwasaki, F.1
Miharu, M.2
Hirano, N.3
Saijyo, M.4
Tani, S.5
Kunishima, M.6
Terao, K.7
-
38
-
-
78049330509
-
-
Phenyl thio-α-cellobioside 4 was found to be the best acceptor for an EGIII-catalysed lactosylation reaction using β-lactosyl fluoride as a glycosyl donor in comparison with α-glucoside, β-glucoside, and β-cellobioside, which will be reported elsewhere
-
Phenyl thio-α-cellobioside 4 was found to be the best acceptor for an EGIII-catalysed lactosylation reaction using β-lactosyl fluoride as a glycosyl donor in comparison with α-glucoside, β-glucoside, and β-cellobioside, which will be reported elsewhere.
-
-
-
-
40
-
-
0031890507
-
-
H. Okada K. Tada T. Sekiya K. Yokoyama A. Takahashi H. Tohda H. Kumagai Y. Morikawa Appl. Environ. Microbiol. 1998 64 555 563
-
(1998)
Appl. Environ. Microbiol.
, vol.64
, pp. 555-563
-
-
Okada, H.1
Tada, K.2
Sekiya, T.3
Yokoyama, K.4
Takahashi, A.5
Tohda, H.6
Kumagai, H.7
Morikawa, Y.8
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