-
1
-
-
9344227358
-
A strain-promoted [3+2] azide-alkyne cycloaddition for covalent modification of biomolecules in living systems
-
Agard N.J., Prescher J.A., Bertozzi C.R. A strain-promoted [3+2] azide-alkyne cycloaddition for covalent modification of biomolecules in living systems. J. Am. Chem. Soc. 2004, 126:15046-15047.
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 15046-15047
-
-
Agard, N.J.1
Prescher, J.A.2
Bertozzi, C.R.3
-
2
-
-
37049101308
-
Dynamic stereochemistry of imines and derivatives. Part 11. Synthesis and stereochemistry of (E)- and (Z)-nitrones
-
Bjørgo J., Boyd D.R., Neill D.C., Jennings W.B. Dynamic stereochemistry of imines and derivatives. Part 11. Synthesis and stereochemistry of (E)- and (Z)-nitrones. J. Chem. Soc. Perkin Trans. I 1977, 3:254-259.
-
(1977)
J. Chem. Soc. Perkin Trans. I
, vol.3
, pp. 254-259
-
-
Bjørgo, J.1
Boyd, D.R.2
Neill, D.C.3
Jennings, W.B.4
-
3
-
-
77958060431
-
Nature's reaction enforcer-comparative effects for organic synthesis "in-water" and "on-water"
-
Butler R.N., Coyne A.G. Nature's reaction enforcer-comparative effects for organic synthesis "in-water" and "on-water". Chem. Rev. 2010, 110:6302-6337.
-
(2010)
Chem. Rev.
, vol.110
, pp. 6302-6337
-
-
Butler, R.N.1
Coyne, A.G.2
-
4
-
-
0002294391
-
The [3+2] nitrone-olefine cycloaddition reaction
-
Confalone P.N., Huie E.M. The [3+2] nitrone-olefine cycloaddition reaction. Org. React. 1988, 36:1-174.
-
(1988)
Org. React.
, vol.36
, pp. 1-174
-
-
Confalone, P.N.1
Huie, E.M.2
-
5
-
-
0001674538
-
Geometrical and stereochemical factors in metal-promoted amide hydrolysis
-
Groves J.T., Chambers R.R.J. Geometrical and stereochemical factors in metal-promoted amide hydrolysis. J. Am. Chem. Soc. 1984, 106:630-638.
-
(1984)
J. Am. Chem. Soc.
, vol.106
, pp. 630-638
-
-
Groves, J.T.1
Chambers, R.R.J.2
-
7
-
-
36749014055
-
1.3-Dipolar cycloadditions. Past and future
-
Huisgen R. 1.3-Dipolar cycloadditions. Past and future. Angew. Chem. Int. Ed. 1963, 2:565-598.
-
(1963)
Angew. Chem. Int. Ed.
, vol.2
, pp. 565-598
-
-
Huisgen, R.1
-
8
-
-
84981759690
-
Kinetik und Mechanismen der Nitron-Additionen an ungesättigte Verbindungen
-
Huisgen R., Seidl H., Brüning I. Kinetik und Mechanismen der Nitron-Additionen an ungesättigte Verbindungen. Chem. Ber. 1969, 102:1102-1116.
-
(1969)
Chem. Ber.
, vol.102
, pp. 1102-1116
-
-
Huisgen, R.1
Seidl, H.2
Brüning, I.3
-
9
-
-
0041791025
-
Substituent effect of dipole and dipolarophile in the reaction of nitrones with N-(substituted phenyl)maleimides
-
Iwakura Y., Uno K., Hong S.-J., Hongu T. Substituent effect of dipole and dipolarophile in the reaction of nitrones with N-(substituted phenyl)maleimides. Bull. Chem. Soc. Jpn. 1972, 45:192-195.
-
(1972)
Bull. Chem. Soc. Jpn.
, vol.45
, pp. 192-195
-
-
Iwakura, Y.1
Uno, K.2
Hong, S.-J.3
Hongu, T.4
-
12
-
-
0000096835
-
Click chemistry: Diverse chemical function from a few good reactions
-
Kolb H.C., Finn M.G., Sharpless K.B. Click chemistry: Diverse chemical function from a few good reactions. Angew. Chem Int. Ed. 2001, 40:2004-2021.
-
(2001)
Angew. Chem Int. Ed.
, vol.40
, pp. 2004-2021
-
-
Kolb, H.C.1
Finn, M.G.2
Sharpless, K.B.3
-
14
-
-
33746820191
-
18F]fluoropeptides using Cu(I) catalyzed 1.3-dipolar cycloaddition
-
18F]fluoropeptides using Cu(I) catalyzed 1.3-dipolar cycloaddition. Tetrahedron Lett. 2006, 47(37):6681-6684.
-
(2006)
Tetrahedron Lett.
, vol.47
, Issue.37
, pp. 6681-6684
-
-
Marik, J.1
Sutcliffe, J.L.2
-
15
-
-
78649870232
-
Cycloaddition reactions in aqueous systems: A two-decade trend endeavour
-
Moulay S., Touati A. Cycloaddition reactions in aqueous systems: A two-decade trend endeavour. C. R. Chim. 2010, 13:1474-1511.
-
(2010)
C. R. Chim.
, vol.13
, pp. 1474-1511
-
-
Moulay, S.1
Touati, A.2
-
16
-
-
77951159275
-
Protein modification by strain-promoted alkyne-nitrone cycloaddition
-
Ning X., Temming R.P., Dommerholt J., et al. Protein modification by strain-promoted alkyne-nitrone cycloaddition. Angew. Chem. Int. Ed. 2010, 49(17):3065-3068.
-
(2010)
Angew. Chem. Int. Ed.
, vol.49
, Issue.17
, pp. 3065-3068
-
-
Ning, X.1
Temming, R.P.2
Dommerholt, J.3
-
17
-
-
10644242798
-
Self-replication vs. reactive binary complexes-manipulating recognition-mediated cyclo additions by simple structural modifications
-
Pearson R.J., Kassianidis E., Slawin A.M.Z., Philp D. Self-replication vs. reactive binary complexes-manipulating recognition-mediated cyclo additions by simple structural modifications. Org. Biomol. Chem. 2004, 2:3434-3441.
-
(2004)
Org. Biomol. Chem.
, vol.2
, pp. 3434-3441
-
-
Pearson, R.J.1
Kassianidis, E.2
Slawin, A.M.Z.3
Philp, D.4
-
18
-
-
70450181011
-
Microwave-assisted 1.3-dipolar cycloaddition: an eco-friendly approach to five-membered heterocycles
-
Pineiro M., Pinho e Melo T.M.V.D. Microwave-assisted 1.3-dipolar cycloaddition: an eco-friendly approach to five-membered heterocycles. Eur. J. Org. Chem. 2009, 5287-5307.
-
(2009)
Eur. J. Org. Chem.
, pp. 5287-5307
-
-
Pineiro, M.1
Pinho e Melo, T.M.V.D.2
-
19
-
-
17644409095
-
Head-to-Tail Peptide Cyclodimerization by copper-catalyzed azide-alkyne cycloaddition
-
Punna S., Kuzelka J., Wang Q., Finn M.G. Head-to-Tail Peptide Cyclodimerization by copper-catalyzed azide-alkyne cycloaddition. Angew. Chem. Int. Ed. 2005, 44:2215-2220.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 2215-2220
-
-
Punna, S.1
Kuzelka, J.2
Wang, Q.3
Finn, M.G.4
-
20
-
-
0014006853
-
The mechanism of nitrone formation. A defense of anthromorphic electrons
-
Reimann J.E., Jencks W.P. The mechanism of nitrone formation. A defense of anthromorphic electrons. J. Am. Chem. Soc. 1966, 88(17):3973-3982.
-
(1966)
J. Am. Chem. Soc.
, vol.88
, Issue.17
, pp. 3973-3982
-
-
Reimann, J.E.1
Jencks, W.P.2
-
21
-
-
0016754770
-
Alkylating derivatives of amino acids and peptides. Synthesis of N-maleoylamino acids, [1-(N-maleoylglycyl)cysteinyl]oxytocin, and [1-(N-maleoyl-11-aminoundecanoyl)cysteinyl]-oxytocin. Effects on vasopressin-stimulated water loss from isolated toad bladder
-
Rich D.H., Gesellchen P.D., Tong A., Cheung A., Buchner C.K. Alkylating derivatives of amino acids and peptides. Synthesis of N-maleoylamino acids, [1-(N-maleoylglycyl)cysteinyl]oxytocin, and [1-(N-maleoyl-11-aminoundecanoyl)cysteinyl]-oxytocin. Effects on vasopressin-stimulated water loss from isolated toad bladder. J. Med. Chem. 1975, 18:1004-1010.
-
(1975)
J. Med. Chem.
, vol.18
, pp. 1004-1010
-
-
Rich, D.H.1
Gesellchen, P.D.2
Tong, A.3
Cheung, A.4
Buchner, C.K.5
-
22
-
-
0037099395
-
A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
-
Rostovtsev V.V., Green L.G., Fokin V.V., Sharpless K.B. A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. Angew. Chem. Int. Ed. 2002, 41:2596-2599.
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 2596-2599
-
-
Rostovtsev, V.V.1
Green, L.G.2
Fokin, V.V.3
Sharpless, K.B.4
-
23
-
-
0038575277
-
1.3-Dipolar Cycloaddition Reactions of Nitrones to Prop-1-ene-1.3-sultone
-
Tian L., Xu G., Ye Y.L.L. 1.3-Dipolar Cycloaddition Reactions of Nitrones to Prop-1-ene-1.3-sultone. Synth. 2003, 1329-1334.
-
(2003)
Synth.
, pp. 1329-1334
-
-
Tian, L.1
Xu, G.2
Ye, Y.L.L.3
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