-
1
-
-
0026637316
-
Structure and function of the mannose 6-phosphate insulin-like growth factor-ii receptors
-
Kornfeld, S. Structure and function of the mannose 6-phosphate insulin-like growth factor-ii receptors. Annu. Rev. Biochem. 1992, 61, 307-330.
-
(1992)
Annu. Rev. Biochem.
, vol.61
, pp. 307-330
-
-
Kornfeld, S.1
-
2
-
-
0032506124
-
Retinoic acid alters the intracellular trafficking of the mannose-6-phosphate insulin-like growth factor II receptor and lysosomal enzymes
-
Kang, J.K.; Li, Y.; Leaf, A. Retinoic acid alters the intracellular trafficking of the mannose-6-phosphate insulin-like growth factor II receptor and lysosomal enzymes. Proc. Natl. Acad. Sci. USA 1998, 95, 13671-13676.
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 13671-13676
-
-
Kang, J.K.1
Li, Y.2
Leaf, A.3
-
3
-
-
0029793594
-
The insulin-like growth factor II mannose 6-phosphate receptor is required for proliferin-induced angiogenesis
-
Volpert, A.; Jackson, D.; Bouck, N.; Linzer, D.I.H. The insulin-like growth factor II mannose 6-phosphate receptor is required for proliferin-induced angiogenesis. Endocrinology 1996, 137, 3871-3876.
-
(1996)
Endocrinology
, vol.137
, pp. 3871-3876
-
-
Volpert, A.1
Jackson, D.2
Bouck, N.3
Linzer, D.I.H.4
-
4
-
-
80053396577
-
Synthesis of Mannose-6-Phosphate analogues and their utility as angiogenesis regulators
-
Barragan-Montero, V.; Awwad, A.; Combemale, S.; de Santa Barbara, P.; Jover, B.; Molès, J.-P.; Montero, J.-L. Synthesis of Mannose-6-Phosphate analogues and their utility as angiogenesis regulators. Chem. Med. Chem. 2011, 6, 1771-1774.
-
(2011)
Chem. Med. Chem.
, vol.6
, pp. 1771-1774
-
-
Barragan-Montero, V.1
Awwad, A.2
Combemale, S.3
De Santa Barbara, P.4
Jover, B.5
Molès, J.-P.6
Montero, J.-L.7
-
5
-
-
84893147330
-
Novel uses of D-Mannopyranose derivatives
-
19 November
-
Clavel, C.; de Santa Barbara, P.; Jover, B.; Moles, J.-P.; Montero, J.-L.; Montero, V. Novel Uses of D-Mannopyranose Derivatives. U.S. Patent WO 2009138601 A2, 19 November 2009.
-
(2009)
U.S. Patent WO 2009138601 A2
-
-
Clavel, C.1
De Santa Barbara, P.2
Jover, B.3
Moles, J.-P.4
Montero, J.-L.5
Montero, V.6
-
6
-
-
84893107607
-
-
EP 2499150 A1, 19 September
-
Awwad, A.; Combemale, S.; de Santa Barbara, P.; Jover, B.; Molès, J.-P.; Montero, J.-L.; Barragan-Montero, V. Nouveaux Derives de Mannopyranoside Ayant une Activite Anticancereuse. EP 2499150 A1, 19 September 2012.
-
(2012)
Nouveaux Derives de Mannopyranoside Ayant une Activite Anticancereuse.
-
-
Awwad, A.1
Combemale, S.2
De Santa Barbara, P.3
Jover, B.4
Molès, J.-P.5
Montero, J.-L.6
Barragan-Montero, V.7
-
7
-
-
84893099881
-
-
EP 2285817 A2, 23 February
-
De Santa Barbara, P.; Jover, B.; Moles, J.-P.; Montero, J.-L.; Montero, V. Nouvelles Utilisations de Derives de D-Mannopyranose Activateurs de l'angiogenese. EP 2285817 A2, 23 February 2011.
-
(2011)
Nouvelles Utilisations de Derives de D-Mannopyranose Activateurs de l'angiogenese.
-
-
De Santa Barbara, P.1
Jover, B.2
Moles, J.-P.3
Montero, J.-L.4
Montero, V.5
-
8
-
-
30744459253
-
-
Wong C.-H. Ed.; Wiley-VCH: Weinheim, Germany
-
Kitov, P.I.; Bundle, D.R. Carbohydrate-Based Drug Discovery; Wong, C.-H., Ed.; Wiley-VCH: Weinheim, Germany, 2003; Volume 2, pp. 541-574.
-
(2003)
Carbohydrate-Based Drug Discovery
, vol.2
, pp. 541-574
-
-
Kitov, P.I.1
Bundle, D.R.2
-
9
-
-
4143069261
-
-
Wong C.-H. Ed.; Wiley-VCH: Weinheim, Germany
-
Kiessling, L.L.; Pontrello, J.K.; Schuster, M.C. Carbohydrate-Based Drug Discovery; Wong, C.-H., Ed.; Wiley-VCH: Weinheim, Germany, 2003; Volume 2, pp. 575-608.
-
(2003)
Carbohydrate-Based Drug Discovery
, vol.2
, pp. 575-608
-
-
Kiessling, L.L.1
Pontrello, J.K.2
Schuster, M.C.3
-
10
-
-
33746296180
-
Synthetic multivalent ligands as probes of signal transduction
-
Kiessling, L.; Gestwicki, J.E.; Strong, L.E. Synthetic multivalent ligands as probes of signal transduction. Angew. Chem. Int. Ed. 2006, 45, 2348-2368.
-
(2006)
Angew. Chem. Int. Ed.
, vol.45
, pp. 2348-2368
-
-
Kiessling, L.1
Gestwicki, J.E.2
Strong, L.E.3
-
11
-
-
0000358206
-
Synthetic multivalent ligands as probes of signal transduction
-
Lee, Y.; Lee, C.R.T. Synthetic multivalent ligands as probes of signal transduction. Acc. Chem. Res. 1995, 28, 321-327.
-
(1995)
Acc. Chem. Res.
, vol.28
, pp. 321-327
-
-
Lee, Y.1
Lee, C.R.T.2
-
12
-
-
11544358874
-
Lectins: Carbohydrate-specific proteins that mediate cellular recognition
-
Lis, H.; Sharon, N. Lectins: Carbohydrate-specific proteins that mediate cellular recognition. Chem. Rev. 1998, 98, 637-674.
-
(1998)
Chem. Rev.
, vol.98
, pp. 637-674
-
-
Lis, H.1
Sharon, N.2
-
13
-
-
0036462602
-
The cluster glycoside effect
-
Lundquist, J.J.; Toone, E.J. The cluster glycoside effect. Chem. Rev. 2002, 102, 555-578.
-
(2002)
Chem. Rev.
, vol.102
, pp. 555-578
-
-
Lundquist, J.J.1
Toone, E.J.2
-
14
-
-
0035907920
-
Gold glyconanoparticles as water-soluble polyvalent models to study carbohydrate interactions
-
De La Fuente, J.M.; Barrientos, A.G.; Rojas, T.C.; Rojo, J.; Cañada, J.; Fernández, A.; Penadés, S. Gold glyconanoparticles as water-soluble polyvalent models to study carbohydrate interactions. Angew. Chem. Int. Ed. 2001, 40, 2257-2261.
-
(2001)
Angew. Chem. Int. Ed.
, vol.40
, pp. 2257-2261
-
-
De La Fuente, J.M.1
Barrientos, A.G.2
Rojas, T.C.3
Rojo, J.4
Cañada, J.5
Fernández, A.6
Penadés, S.7
-
15
-
-
0002490493
-
-
Padwa, A., Ed.; Wiley-VCH: Weinheim, Germany
-
Huisgen, R. 1,3-Dipolar Cycloaddition Chemistry; Padwa, A., Ed.; Wiley-VCH: Weinheim, Germany, 1984; Volume 1, pp. 1-176.
-
(1984)
1,3-Dipolar Cycloaddition Chemistry
, vol.1
, pp. 1-176
-
-
Huisgen, R.1
-
16
-
-
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
-
17
-
-
0348109450
-
The growing impact of click chemistry on drug discovery
-
Kolb, H.C.; Sharpless, K.B. The growing impact of click chemistry on drug discovery. Drug Discov. Today 2003, 8, 1128-1137.
-
(2003)
Drug Discov. Today
, vol.8
, pp. 1128-1137
-
-
Kolb, H.C.1
Sharpless, K.B.2
-
18
-
-
80055005707
-
Click-chemistry for nanoparticle-modification
-
Li, N.; Binder, W.H. Click-chemistry for nanoparticle-modification. Mater. Chem. 2011, 21, 16717-16734.
-
(2011)
Mater. Chem.
, vol.21
, pp. 16717-16734
-
-
Li, N.1
Binder, W.H.2
-
19
-
-
0002726406
-
-
Patai, S., Ed.; Interscience Publishers: London, UK
-
Bastide, J.; Henri-Rousseau, O. The Chemistry of the Carbon-Carbon Triple Bond; Patai, S., Ed.; Interscience Publishers: London, UK, 1978; pp. 447-552.
-
(1978)
The Chemistry of the Carbon-Carbon Triple Bond
, pp. 447-552
-
-
Bastide, J.1
Henri-Rousseau, O.2
-
20
-
-
0037012920
-
Peptidotriazoles on solid phase: [1,23]-triazoles by regiospecific copper(I)-catalyzed 13-dipolar cycloadditions of terminal alkynes to azides
-
Tornøe, W.; Christensen, C.; Meldal, M. Peptidotriazoles on solid phase: [1,2,3]-triazoles by regiospecific copper(I)-catalyzed 1,3-dipolar cycloadditions of terminal alkynes to azides. J. Org. Chem. 2002, 67, 3057-3064.
-
(2002)
J Org Chem
, vol.67
, pp. 3057-3064
-
-
Tornøe, W.1
Christensen, C.2
Meldal, M.3
-
21
-
-
37049059528
-
Chemotherapy of schistosomiasis. V. Cholesteryl and choloyl derivatives of 4-Amino-2-methoxyphenyl ethers
-
Davis, M. Chemotherapy of schistosomiasis. V. Cholesteryl and choloyl derivatives of 4-Amino-2-methoxyphenyl ethers. J. Chem. Soc. 1962, 1962, 178-181.
-
(1962)
J. Chem. Soc.
, vol.1962
, pp. 178-181
-
-
Davis, M.1
-
22
-
-
0000941676
-
Decomposition of reducing disaccharides, VII Determination of the constitution of maltose
-
Zemplén, G. Decomposition of reducing disaccharides, VII Determination of the constitution of maltose. Berich. Deutschen Chem. Gesellsch. 1927, 7, 1555-1564.
-
(1927)
Berich. Deutschen Chem. Gesellsch.
, vol.7
, pp. 1555-1564
-
-
Zemplén, G.1
-
23
-
-
0037182229
-
Synthesis of mannose-6-phosphate analogs: Large-scale preparation of isosteric mannose-6-phosphonate via cyclic sulfate precursor
-
Khanjin, N.A.; Montero, J.-L. Synthesis of mannose-6-phosphate analogs: Large-scale preparation of isosteric mannose-6-phosphonate via cyclic sulfate precursor. Tetrahedron Lett. 2002, 43, 4017-4020.
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 4017-4020
-
-
Khanjin, N.A.1
Montero, J.-L.2
-
24
-
-
0000856304
-
Cyclic sulfates containing acid-sensitive groups and chemoselective hydrolysis of sulfate esters
-
Kim, B.M.; Sharpless, K.B. Cyclic sulfates containing acid-sensitive groups and chemoselective hydrolysis of sulfate esters. Tetrahedron Lett. 1989, 30, 655-658.
-
(1989)
Tetrahedron Lett.
, vol.30
, pp. 655-658
-
-
Kim, B.M.1
Sharpless, K.B.2
-
25
-
-
0001743755
-
Phase-transfer synthesis of mono-Alkyl ethers of oligoethylene glycols
-
Gibson, T. Phase-transfer synthesis of mono-Alkyl ethers of oligoethylene glycols. J. Org. Chem. 1980, 45, 1095-1098.
-
(1980)
J. Org. Chem.
, vol.45
, pp. 1095-1098
-
-
Gibson, T.1
-
26
-
-
37049177210
-
The addition of thio-compounds to olefins. II. Reactions of thiolacetic and mono-chlorothiolacetic, di-chlorothiolacetic, and tri-chlorothiolacetic acids
-
Cunneen, J.I. The addition of thio-compounds to olefins. II. Reactions of thiolacetic and mono-chlorothiolacetic, di-chlorothiolacetic, and tri-chlorothiolacetic acids. J. Chem. Soc. 1947, 1947, 134-141.
-
(1947)
J. Chem. Soc.
, vol.1947
, pp. 134-141
-
-
Cunneen, J.I.1
-
27
-
-
49149140261
-
On the equilibrium Cu2++Cu(s) reversible 2Cu+
-
Ciavatta, L.; Ferri, D.; Palombari, R. On the equilibrium Cu2++Cu(s) reversible 2Cu+. J. Inorg. Nucl. Chem. 1980, 42, 593-598.
-
(1980)
J. Inorg. Nucl. Chem.
, vol.42
, pp. 593-598
-
-
Ciavatta, L.1
Ferri, D.2
Palombari, R.3
-
28
-
-
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
-
29
-
-
11844255741
-
Copper (I)-catalyzed synthesis of azoles. DFT study predicts unprecedented reactivity and intermediates
-
Himo, F.; Lovell, T.; Hilgraf, R.; Rostovtsev, V.V.; Noodleman, L.; Sharpless, K.B.; Fokin, V.V. Copper(I)-catalyzed synthesis of azoles. DFT study predicts unprecedented reactivity and intermediates. J. Am. Chem. Soc. 2005, 127, 210-216.
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 210-216
-
-
Himo, F.1
Lovell, T.2
Hilgraf, R.3
Rostovtsev, V.V.4
Noodleman, L.5
Sharpless, K.B.6
Fokin, V.V.7
-
30
-
-
84867726453
-
Cu-I-catalyzed Alkyne-Azide "click" cycloadditions from a mechanistic and synthetic perspective
-
Bock, V.D.; Hiemstra, H.; van Maarseveen, J.H. Cu-I-catalyzed alkyne-Azide "click" cycloadditions from a mechanistic and synthetic perspective. Eur. J. Org. Chem. 2006, 2006, 51-68.
-
(2006)
Eur J. Org. Chem.
, vol.2006
, pp. 51-68
-
-
Bock, V.D.1
Hiemstra, H.2
Van Maarseveen, J.H.3
-
31
-
-
17644414186
-
Mechanism of the ligand-free CuI-catalyzed azide-Alkyne cycloaddition reaction
-
Rodionov, V.O.; Fokin, V.V.; Finn, M.G. Mechanism of the ligand-free CuI-catalyzed azide-Alkyne cycloaddition reaction. Angew. Chem. Int. Ed. 2005, 44, 2210-2215.
-
(2005)
Angew. Chem. Int. Ed.
, vol.44
, pp. 2210-2215
-
-
Rodionov, V.O.1
Fokin, V.V.2
Finn, M.G.3
-
32
-
-
51049094897
-
Cu-catalyzed azide-Alkyne cycloaddition
-
Meldal, M.; Tornøe, C.W. Cu-catalyzed azide-Alkyne cycloaddition. Chem. Rev. 2008, 108, 2952-3015.
-
(2008)
Chem. Rev.
, vol.108
, pp. 2952-3015
-
-
Meldal, M.1
Tornøe, C.W.2
-
33
-
-
34247602441
-
Click chemistry with O-dimethylpropargylcarbamate for preparation of pH-sensitive functional groups. A case study
-
Bertrand, P.; Gesson, J.-P. Click chemistry with O- dimethylpropargylcarbamate for preparation of pH-sensitive functional groups. A case study. J. Org. Chem. 2007, 72, 3596-3599.
-
(2007)
J. Org. Chem.
, vol.72
, pp. 3596-3599
-
-
Bertrand, P.1
Gesson, J.-P.2
-
34
-
-
15944397964
-
Regioselective synthesis of [1,23]-triazoles catalyzed by Cu(I) generated in situ from Cu(0) nanosize activated powder and amine hydrochloride salts
-
Orgueira, H.A.; Fokas, D.; Isome, Y.; Chan, P.C.; Baldino, C.M. Regioselective synthesis of [1,2,3]-triazoles catalyzed by Cu(I) generated in situ from Cu(0) nanosize activated powder and amine hydrochloride salts. Tetrahedron Lett. 2005, 46, 2911-2914.
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 2911-2914
-
-
Orgueira, H.A.1
Fokas, D.2
Isome, Y.3
Chan, P.C.4
Baldino, C.M.5
-
35
-
-
0039174828
-
Frank hexanitrato ammonium cerate as a proposed reference standard in oxidimetry G
-
Smith, G.F.; Sullivan, V.R. Frank, hexanitrato ammonium cerate as a proposed reference standard in oxidimetry G. Ind. Eng. Chem. Anal. Ed. 1936, 8, 449-451.
-
(1936)
Ind. Eng. Chem. Anal. Ed.
, vol.8
, pp. 449-451
-
-
Smith, G.F.1
Sullivan, V.R.2
-
37
-
-
84925497165
-
Zur reaktionsweise des pentaphenyl-phosphors und einiger derivate
-
Wittig, G.; Geissler, G. Zur reaktionsweise des pentaphenyl-phosphors und einiger derivate. Liebigs Ann. Chem. 1953, 580, 44-57.
-
(1953)
Liebigs Ann. Chem.
, vol.580
, pp. 44-57
-
-
Wittig, G.1
Geissler, G.2
-
38
-
-
84979404437
-
Uber triphenyl-phosphinmethylene als olefinbildende reagenzien
-
Wittig, G.; Schöllkopf, U. Uber triphenyl-phosphinmethylene als olefinbildende reagenzien. Chem. Ber. 1954, 87, 1318-1330.
-
(1954)
Chem. Ber.
, vol.87
, pp. 1318-1330
-
-
Wittig, G.1
Schöllkopf, U.2
-
39
-
-
0001848341
-
The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions-stereochemistry, mechanism, and selected synthetic aspects
-
Maryanoff, B.E.; Reitz, A.B. The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions-stereochemistry, mechanism, and selected synthetic aspects. Chem. Rev. 1989, 89, 863-927.
-
(1989)
Chem. Rev.
, vol.89
, pp. 863-927
-
-
Maryanoff, B.E.1
Reitz, A.B.2
-
40
-
-
77956606957
-
Phosphororganische Verbindungen XII. Phosphinoxyde als Olefinierungsreagenzien
-
Horner, L.; Hoffmann, H.; Wippel, H.G. Phosphororganische Verbindungen, XII. Phosphinoxyde als Olefinierungsreagenzien. Chem. Ber. 1958, 91, 61-63.
-
(1958)
Chem. Ber.
, vol.91
, pp. 61-63
-
-
Horner, L.1
Hoffmann, H.2
Wippel, H.G.3
-
41
-
-
77956602917
-
Phosphororganische verbindungen, XX. Phosphinoxyde als olefinierungsreagenzien
-
Horner, L.; Hoffmann, H.; Wippel, H.G.; Klahre, G. Phosphororganische verbindungen, XX. phosphinoxyde als olefinierungsreagenzien. Chem. Ber. 1959, 92, 2499-2505.
-
(1959)
Chem. Ber.
, vol.92
, pp. 2499-2505
-
-
Horner, L.1
Hoffmann, H.2
Wippel, H.G.3
Klahre, G.4
-
42
-
-
0345391556
-
Utility of phosphonate carbanions in olefin synthesis
-
Wadsworth, W.S.; Emmons, W.D. Utility of phosphonate carbanions in olefin synthesis. J. Am. Chem. Soc. 1961, 83, 1733-1738.
-
(1961)
J. Am. Chem. Soc.
, vol.83
, pp. 1733-1738
-
-
Wadsworth, W.S.1
Emmons, W.D.2
-
43
-
-
0003083944
-
Synthetic applications ofphosphoryl-stabilized anions
-
Wadsworth, W.S. Synthetic applications ofphosphoryl-stabilized anions. Org. React. 1977, 25, 73-253.
-
(1977)
Org. React.
, vol.25
, pp. 73-253
-
-
Wadsworth, W.S.1
-
44
-
-
33947317747
-
A carbonyl olefination reaction using silyl-subsituted organometallic compounds
-
Peterson, D.J. A carbonyl olefination reaction using silyl-subsituted organometallic compounds. J. Org. Chem. 1968, 33, 780-784.
-
(1968)
J. Org. Chem.
, vol.33
, pp. 780-784
-
-
Peterson, D.J.1
-
45
-
-
0036251475
-
New developments in the Peterson olefination reaction
-
Van Staden, L.F.; Gravestock, D.; Ager, D.J. New developments in the Peterson olefination reaction. Chem. Soc. Rev. 2002, 31, 195-200.
-
(2002)
Chem. Soc. Rev.
, vol.31
, pp. 195-200
-
-
Van Staden, L.F.1
Gravestock, D.2
Ager, D.J.3
-
46
-
-
0002974335
-
The Peterson olefination reaction
-
Ager, D.J. The Peterson olefination reaction. Org. React. 1990, 38, 1-223.
-
(1990)
Org. React.
, vol.38
, pp. 1-223
-
-
Ager, D.J.1
-
47
-
-
0012203007
-
Olefin synthesis by reductive elimination of ß-hydroxysulfoximines- methylenation of carbonyl-compounds
-
Johnson, C.R.; Shanklin, J.R.; Kirchhoff, R.A. Olefin synthesis by reductive elimination of ß-hydroxysulfoximines-methylenation of carbonyl-compounds. J. Am. Chem. Soc. 1973, 95, 6462-6463.
-
(1973)
J. Am. Chem. Soc.
, vol.95
, pp. 6462-6463
-
-
Johnson, C.R.1
Shanklin, J.R.2
Kirchhoff, R.A.3
-
48
-
-
26444603140
-
Syntheses using sulfones V(+). Method for general synthesis of double bonds
-
Julia, M.; Paris, J.-M. Syntheses using sulfones V(+). Method for general synthesis of double bonds. Tetrahedron Lett. 1973, 14, 4833-4836.
-
(1973)
Tetrahedron Lett.
, vol.14
, pp. 4833-4836
-
-
Julia, M.1
Paris, J.-M.2
-
49
-
-
0026089935
-
A direct synthesis of olefins by reaction of carbonyl-compounds with lithio derivatives of 2-[alkyl-sulfonyl Or (2'-Alkenyl)-sulfonyl Or Benzyl-sulfonyl]-benzothiazoles
-
Baudin, J.B.; Hareau, G.; Julia, S.A.; Ruel, O. A direct synthesis of olefins by reaction of carbonyl-compounds with lithio derivatives of 2-[alkyl-sulfonyl or (2'-Alkenyl)-sulfonyl or benzyl-sulfonyl]-benzothiazoles. Tetrahedron Lett. 1991, 32, 1175-1178.
-
(1991)
Tetrahedron Lett.
, vol.32
, pp. 1175-1178
-
-
Baudin, J.B.1
Hareau, G.2
Julia, S.A.3
Ruel, O.4
-
50
-
-
0001624845
-
Stereochemistry of the olefin formation from anti and syn heterocyclic beta-hydroxy-sulfones
-
Baudin, J.B.; Hareau, G.; Julia, S.A.; Lorne, R.; Ruel, O. Stereochemistry of the olefin formation from anti and syn heterocyclic beta-hydroxy-sulfones. Bull. Soc. Chim. Fr. 1993, 130, 336-357.
-
(1993)
Bull. Soc. Chim. Fr.
, vol.130
, pp. 336-357
-
-
Baudin, J.B.1
Hareau, G.2
Julia, S.A.3
Lorne, R.4
Ruel, O.5
-
51
-
-
0037038993
-
The modified Julia olefination: Alkene synthesis via the condensation of metallated heteroarylalkylsulfones with carbonyl compounds
-
Blakemore, P.R. The modified Julia olefination: Alkene synthesis via the condensation of metallated heteroarylalkylsulfones with carbonyl compounds. J. Chem. Soc. Perkin Trans. 2002, 2002, 2563-2585.
-
(2002)
J. Chem. Soc. Perkin Trans.
, vol.2002
, pp. 2563-2585
-
-
Blakemore, P.R.1
-
52
-
-
33847089541
-
Allylic oxidation of olefins by catalytic and stoichiometric selenium dioxide with tert-butyl hydroperoxide
-
Umbreit, M.A.; Sharpless, K.B. Allylic oxidation of olefins by catalytic and stoichiometric selenium dioxide with tert-butyl hydroperoxide. J. Am. Chem. Soc. 1977, 99, 5526-5528.
-
(1977)
J. Am. Chem. Soc.
, vol.99
, pp. 5526-5528
-
-
Umbreit, M.A.1
Sharpless, K.B.2
-
53
-
-
0004220172
-
-
3rd ed.; Oxford University Press: Oxford, NY, USA
-
Stevens, M.P. Polymer Chemistry, 3rd ed.; Oxford University Press: Oxford, NY, USA, 1999; pp. 265-267.
-
(1999)
Polymer Chemistry
, pp. 265-267
-
-
Stevens, M.P.1
-
54
-
-
0000817415
-
The peroxide effect in the addition of reagents to unsaturated compounds and in rearrangement reactions
-
Mayo, F.R.; Walling, C. The peroxide effect in the addition of reagents to unsaturated compounds and in rearrangement reactions. Chem. Rev. 1940, 27, 351-412.
-
(1940)
Chem. Rev.
, vol.27
, pp. 351-412
-
-
Mayo, F.R.1
Walling, C.2
-
56
-
-
84980124864
-
Information on unsaturated compounds II. The addition of mercaptan to unsaturated hydrocarbon
-
Posner, T. Information on unsaturated compounds II. The addition of mercaptan to unsaturated hydrocarbon. Berich. Deutschen Chem. Gesellsch. 1905, 38, 646-657.
-
(1905)
Berich. Deutschen Chem. Gesellsch.
, vol.38
, pp. 646-657
-
-
Posner, T.1
-
57
-
-
10044258525
-
Integrated nanoparticle-biomolecule hybrid systems: Synthesis, properties, and applications
-
Katz, E.; Willner, I. Integrated nanoparticle-biomolecule hybrid systems: Synthesis, properties, and applications. Angew. Chem. Int. Ed. 2004, 43, 6042-6108.
-
(2004)
Angew. Chem. Int. Ed.
, vol.43
, pp. 6042-6108
-
-
Katz, E.1
Willner, I.2
-
58
-
-
37049074842
-
Synthesis of thiol-derivatized gold nanoparticles in a 2-phase liquid-liquid system
-
Brust, M.; Walker, M.; Bethell, D.; Schiffrin, D.J.; Whyman, R. Synthesis of thiol-derivatized gold nanoparticles in a 2-phase liquid-liquid system. J. Chem. Soc. Chem. Commun. 1994, 7, 801-802.
-
(1994)
J. Chem. Soc. Chem. Commun.
, vol.7
, pp. 801-802
-
-
Brust, M.1
Walker, M.2
Bethell, D.3
Schiffrin, D.J.4
Whyman, R.5
-
59
-
-
33746096072
-
A study of the nucleation and growth processes in the synthesis of colloidal gold
-
Turkevich, J.; Stevenson, P.C.; Hillier, J.A. A study of the nucleation and growth processes in the synthesis of colloidal gold. Disc. Far. Soc. 1951, 11, 55-75.
-
(1951)
Disc. Far. Soc.
, vol.11
, pp. 55-75
-
-
Turkevich, J.1
Stevenson, P.C.2
Hillier, J.A.3
-
60
-
-
0003051583
-
Controlled nucleation for regulation of particle-size in monodisperse gold suspensions
-
Frens, G. Controlled nucleation for regulation of particle-size in monodisperse gold suspensions. Nat. Phys. Sci. 1973, 241, 20-22.
-
(1973)
Nat. Phys. Sci.
, vol.241
, pp. 20-22
-
-
Frens, G.1
-
61
-
-
0019601024
-
Sizing of protein a-colloidal gold probes for immunoelectron microscopy
-
Slot, J.W.; Gueuze, H.J. Sizing of protein a-colloidal gold probes for immunoelectron microscopy. J. Cell Biol. 1981, 90, 533-536.
-
(1981)
J. Cell Biol.
, vol.90
, pp. 533-536
-
-
Slot, J.W.1
Gueuze, H.J.2
-
62
-
-
0028447713
-
Gold sol formation mechanisms-role of colloidal stability
-
Chow, M.K.; Zukoski, C.F. Gold sol formation mechanisms-role of colloidal stability. J. Colloid Interf. Sci. 1994, 165, 97-109.
-
(1994)
J. Colloid Interf. Sci.
, vol.165
, pp. 97-109
-
-
Chow, M.K.1
Zukoski, C.F.2
-
63
-
-
33748547223
-
Turkevich method for gold nanoparticle synthesis revisited
-
Kimling, J.; Maier, M.; Okenve, B.; Kotaidis, V.; Ballot, H.; Plech, A. Turkevich method for gold nanoparticle synthesis revisited. J. Phys. Chem. B 2006, 110, 15700-15707.
-
(2006)
J. Phys. Chem. B
, vol.110
, pp. 15700-15707
-
-
Kimling, J.1
Maier, M.2
Okenve, B.3
Kotaidis, V.4
Ballot, H.5
Plech, A.6
-
64
-
-
57149092304
-
Chick embryo chorioallantoic membrane as a useful tool to study angiogenesis
-
Ribatti, D. Chick embryo chorioallantoic membrane as a useful tool to study angiogenesis. Int. Rev. Cell Mol. Biol. 2008, 270, 181-224.
-
(2008)
Int. Rev. Cell Mol. Biol.
, vol.270
, pp. 181-224
-
-
Ribatti, D.1
-
65
-
-
0038103790
-
Observations on the use of the avian chorioallantoic membrane (CAM) model in investigations into angiogenesis
-
Richardson, M.; Singh, G. Observations on the use of the avian chorioallantoic membrane (CAM) model in investigations into angiogenesis. Curr. Drug Targets Cardiovasc. Haematol. Disord. 2003, 3, 155-185.
-
(2003)
Curr. Drug Targets Cardiovasc. Haematol. Disord.
, vol.3
, pp. 155-185
-
-
Richardson, M.1
Singh, G.2
-
66
-
-
84865041687
-
Chick chorioallantoic membrane (CAM) Assay as an in vivo model to study the effect of newly identified molecules on ovarian cancer invasion and metastasis
-
Lokman, N.A.; Elder, A.S.F.; Ricciardelli, C.; Oehler, M.K. Chick chorioallantoic membrane (CAM) Assay as an in vivo model to study the effect of newly identified molecules on ovarian cancer invasion and metastasis. Int. J. Mol. Sci. 2012, 13, 9959-9970.
-
(2012)
Int. J. Mol. Sci.
, vol.13
, pp. 9959-9970
-
-
Lokman, N.A.1
Elder, A.S.F.2
Ricciardelli, C.3
Oehler, M.K.4
|