-
3
-
-
0034624685
-
-
M. J. Genin D. A. Allwine D. J. Anderson M. R. Barbachyn D. E. Emmert S. A. Garmon D. R. Graber K. C. Grega J. B. Hester D. K. Hutchinson J. Morris R. J. Reischer C. W. Ford G. E. Zurenko J. C. Hamel R. D. Schaadt D. Stapert B. H. Yagi J. Med. Chem. 2000 43 953
-
(2000)
J. Med. Chem.
, vol.43
, pp. 953
-
-
Genin, M.J.1
Allwine, D.A.2
Anderson, D.J.3
Barbachyn, M.R.4
Emmert, D.E.5
Garmon, S.A.6
Graber, D.R.7
Grega, K.C.8
Hester, J.B.9
Hutchinson, D.K.10
Morris, J.11
Reischer, R.J.12
Ford, C.W.13
Zurenko, G.E.14
Hamel, J.C.15
Schaadt, R.D.16
Stapert, D.17
Yagi, B.H.18
-
4
-
-
0028063421
-
-
R. Alvarez S. Velazquez A. San-Felix S. Aquaro E. De Clercq C. F. Perno A. Karlsson J. Balzariniand M. J. Camarasa J. Med. Chem. 1994 37 4185
-
(1994)
J. Med. Chem.
, vol.37
, pp. 4185
-
-
Alvarez, R.1
Velazquez, S.2
San-Felix, A.3
Aquaro, S.4
De Clercq, E.5
Perno, C.F.6
Karlsson, A.7
Balzariniand, J.8
Camarasa, M.J.9
-
5
-
-
0033623166
-
-
L. L. Brockunier E. R. Parmee H. O. Ok M. R. Candelore M. A. Cascieri L. F. Colwell L. Deng W. P. Feeney M. J. Forrest G. J. Hom D. E. MacIntyre L. Tota M. J. Wyvratt M. H. Fisher A. E. Weber Bioorg. Med. Chem. Lett. 2000 10 2111
-
(2000)
Bioorg. Med. Chem. Lett.
, vol.10
, pp. 2111
-
-
Brockunier, L.L.1
Parmee, E.R.2
Ok, H.O.3
Candelore, M.R.4
Cascieri, M.A.5
Colwell, L.F.6
Deng, L.7
Feeney, W.P.8
Forrest, M.J.9
Hom, G.J.10
Macintyre, D.E.11
Tota, L.12
Wyvratt, M.J.13
Fisher, M.H.14
Weber, A.E.15
-
6
-
-
84943402961
-
-
ed. A. R. Katritzky and C. W. Rees, Pergamon, Oxford, p.
-
H. Wamhoff, in Comprehensive Heterocyclic Chemistry, ed., A. R. Katritzky, and, C. W. Rees, Pergamon, Oxford, 1984, vol. 5, p. 669
-
(1984)
Comprehensive Heterocyclic Chemistry
, vol.5
, pp. 669
-
-
Wamhoff, H.1
-
13
-
-
54349127381
-
-
S. S. van Berkel A. J. Dirks S. A. Meeuwissen D. L. L. Pingen O. C. Boerman P. Laverman F. L. van Delft J. J. L. M. Cornelissen F. P. J. T. Rutjes ChemBioChem 2008 9 1805
-
(2008)
ChemBioChem
, vol.9
, pp. 1805
-
-
Van Berkel, S.S.1
Dirks, A.J.2
Meeuwissen, S.A.3
Pingen, D.L.L.4
Boerman, O.C.5
Laverman, P.6
Van Delft, F.L.7
Cornelissen, J.J.L.M.8
Rutjes, F.P.J.T.9
-
14
-
-
84906218560
-
-
E. M. Alexandrino P. Buchold M. Wagner A. Fuchs A. Kreyes C. K. Weiss K. Landfester F. R. Wurm Chem. Commun. 2014 50 10495
-
(2014)
Chem. Commun.
, vol.50
, pp. 10495
-
-
Alexandrino, E.M.1
Buchold, P.2
Wagner, M.3
Fuchs, A.4
Kreyes, A.5
Weiss, C.K.6
Landfester, K.7
Wurm, F.R.8
-
17
-
-
28044465418
-
-
L. Zhang X. Chen P. Xue H. H. Y. Sun I. D. Williams K. B. Sharpless V. V. Fokin G. Jia J. Am. Chem. Soc. 2005 127 15998
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 15998
-
-
Zhang, L.1
Chen, X.2
Xue, P.3
Sun, H.H.Y.4
Williams, I.D.5
Sharpless, K.B.6
Fokin, V.V.7
Jia, G.8
-
32
-
-
84875971203
-
-
F. Nador M. A. Volpe F. Alonso A. Feldhoff A. Kirschning G. Radivoy Appl. Catal., A 2013 455 39
-
(2013)
Appl. Catal., A
, vol.455
, pp. 39
-
-
Nador, F.1
Volpe, M.A.2
Alonso, F.3
Feldhoff, A.4
Kirschning, A.5
Radivoy, G.6
-
36
-
-
84906762130
-
-
Only one contribution concerning the specific click reaction for carbohydrate derivatives is known
-
C. Deraedt N. Pinaud D. Astruc J. Am. Chem. Soc. 2014 136 12092
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 12092
-
-
Deraedt, C.1
Pinaud, N.2
Astruc, D.3
-
38
-
-
84887577682
-
-
The concentration of the different surfactants (180 mM) was chosen comparable to that of the organic substrates and above the c.m.c. of all surfactants. TPGS-750-M is commercially available as a 2% (w/w) solution in water and this solution was used directly as a solvent
-
B. H. Lipshutz Z. BoŠković C. S. Crowe V. K. Davis H. C. Whittemore D. A. Vosburg A. G. Wenzel J. Chem. Educ. 2013 90 1514
-
(2013)
J. Chem. Educ.
, vol.90
, pp. 1514
-
-
Lipshutz, B.H.1
Bošković, Z.2
Crowe, C.S.3
Davis, V.K.4
Whittemore, H.C.5
Vosburg, D.A.6
Wenzel, A.G.7
-
48
-
-
84890792871
-
-
Conversely, the reaction was sluggish as expected with terminal sterically hindered alkynes bearing substituents close to the triple bond like in the case of 3,3-dimethyl-1-butyne, ethynyl cyclopentene, ethynyl cyclohexane or with internal alkynes like 1-phenyl-1-propyne
-
X. Fan N. Li T. Shen X.-M. Cui H. Lv H.-B. Zhu Y.-H. Guan Tetrahedron 2014 70 256
-
(2014)
Tetrahedron
, vol.70
, pp. 256
-
-
Fan, X.1
Li, N.2
Shen, T.3
Cui, X.-M.4
Lv, H.5
Zhu, H.-B.6
Guan, Y.-H.7
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