-
1
-
-
0026059272
-
Stereospecific method to (E) and (Z) terminal fluoroolefins and its application to the synthesis of 2′-Deoxy-2′- fluoromethylenenucleosides as potential inhibitors of ribonucleoside diphosphate reductase
-
McCarthy, J.R.; Matthews, D.P.; Stemerick, D.M.; Huber, E.W.; Bey, P.; et al. Stereospecific method to (E) and (Z) terminal fluoroolefins and its application to the synthesis of 2′-Deoxy-2′- fluoromethylenenucleosides as potential inhibitors of ribonucleoside diphosphate reductase. J. Am. Chem. Soc. 1991, 113, 7439-7440.
-
(1991)
J. Am. Chem. Soc.
, vol.113
, pp. 7439-7440
-
-
McCarthy, J.R.1
Matthews, D.P.2
Stemerick, D.M.3
Huber, E.W.4
Bey, P.5
-
2
-
-
33745823841
-
Ribonucleotide reductase inhibitors and future drug design
-
Shao, J.; Zhou, B.; Chu, B.; Yen, Y. Ribonucleotide reductase inhibitors and future drug design. Curr. Cancer Drug Targets 2006, 6, 409-431.
-
(2006)
Curr. Cancer Drug Targets
, vol.6
, pp. 409-431
-
-
Shao, J.1
Zhou, B.2
Chu, B.3
Yen, Y.4
-
3
-
-
0028104514
-
Nucleic acid-related compounds. 84. Synthesis of 6′-(E and Z)-halohomovinyl derivatives of adenosine, inactivation of S-adenosyl-L- homocysteine hydrolase, and correlation of anticancer and antiviral potencies with enzyme inhibition
-
Wnuk, S.F.; Yuan, C.-S.; Borchardt, R.T.; Balzarini, J.; De Clercq, E.; Robins, M.J. Nucleic acid-related compounds. 84. Synthesis of 6′-(E and Z)-halohomovinyl derivatives of adenosine, inactivation of S-adenosyl-L- homocysteine hydrolase, and correlation of anticancer and antiviral potencies with enzyme inhibition. J. Med. Chem. 1994, 37, 3579-3587.
-
(1994)
J. Med. Chem.
, vol.37
, pp. 3579-3587
-
-
Wnuk, S.F.1
Yuan, C.-S.2
Borchardt, R.T.3
Balzarini, J.4
De Clercq, E.5
Robins, M.J.6
-
4
-
-
0028079891
-
(E)-5′,6′-Didehydro-6′-deoxy-6′- fluorohomoadenosine: A substrate that measures the hydrolytic activity of S-adenosylhomocysteine hydrolase
-
Yuan, C.-S.; Wnuk, S.F.; Liu, S.; Robins, M.J.; Borchardt, R.T. (E)-5′,6′-Didehydro-6′-deoxy-6′- fluorohomoadenosine: A substrate that measures the hydrolytic activity of S-adenosylhomocysteine hydrolase. Biochemistry 1994, 33, 12305-12311.
-
(1994)
Biochemistry
, vol.33
, pp. 12305-12311
-
-
Yuan, C.-S.1
Wnuk, S.F.2
Liu, S.3
Robins, M.J.4
Borchardt, R.T.5
-
5
-
-
0028268586
-
Mechanism of inactivation of Sadenosylhomocysteine hydrolase by (E)-5′,6′-didehydro-6′-deoxy-6′-halohomoadenosines
-
Yuan, C.-S.; Liu, S.; Wnuk, S.F.; Robins, M.J.; Borchardt, R.T. Mechanism of inactivation of Sadenosylhomocysteine hydrolase by (E)-5′,6′- didehydro-6′-deoxy-6′-halohomoadenosines. Biochemistry 1994, 33, 3758-3765.
-
(1994)
Biochemistry
, vol.33
, pp. 3758-3765
-
-
Yuan, C.-S.1
Liu, S.2
Wnuk, S.F.3
Robins, M.J.4
Borchardt, R.T.5
-
6
-
-
0027241111
-
Nucleic acid related compounds. 78. Stereocontrolled syntheses of 6′(E and Z)-halovinyl analogs from uridine-derived vinylsulfones via vinyltin intermediates
-
Wnuk, S.F.; Robins, M.J. Nucleic acid related compounds. 78. Stereocontrolled syntheses of 6′(E and Z)-halovinyl analogs from uridine-derived vinylsulfones via vinyltin intermediates. Can. J. Chem. 1993, 71, 192-198.
-
(1993)
Can. J. Chem.
, vol.71
, pp. 192-198
-
-
Wnuk, S.F.1
Robins, M.J.2
-
7
-
-
4444343688
-
Synthesis and biological activities of 5′-ethylenic and acetylenic modified L-nucleosides and isonucleosides
-
Wang, J.-F.; Yang, X.-D.; Zhang, L.-R.; Yang, Z.-J.; Zhang, L.-H. Synthesis and biological activities of 5′-ethylenic and acetylenic modified L-nucleosides and isonucleosides. Tetrahedron 2004, 60, 8535-8546.
-
(2004)
Tetrahedron
, vol.60
, pp. 8535-8546
-
-
Wang, J.-F.1
Yang, X.-D.2
Zhang, L.-R.3
Yang, Z.-J.4
Zhang, L.-H.5
-
8
-
-
0032548968
-
Nucleic acid related compounds. 101. S-Adenosyl-L-homocysteine hydrolase does not hydrate (5′-fluoro)vinyl or (6′-halo)homovinyl analogs derived from 3′-deoxyadenosine or 3′-(chloro or fluoro)-3′- deoxyadenosine
-
Robins, M.J.; Neschadimenko, V.; Ro, B.-O.; Yuan, C.-S.; Borchardt, R.T.; Wnuk, S.F. Nucleic acid related compounds. 101. S-Adenosyl-L-homocysteine hydrolase does not hydrate (5′-fluoro)vinyl or (6′-halo)homovinyl analogs derived from 3′-deoxyadenosine or 3′-(chloro or fluoro)-3′- deoxyadenosine. J. Org. Chem. 1998, 63, 1205-1211.
-
(1998)
J. Org. Chem.
, vol.63
, pp. 1205-1211
-
-
Robins, M.J.1
Neschadimenko, V.2
Ro, B.-O.3
Yuan, C.-S.4
Borchardt, R.T.5
Wnuk, S.F.6
-
9
-
-
33645389725
-
Antitrypanosomal activity of 5′-deoxy-5′-(iodo-methylene) adenosine and Related 6-N-cyclopropyl-adenosine analogs
-
Rapp, M.; Haubrich, T.A.; Perrault, J.; Mackey, Z.B.; McKerrow, J.H.; et al. Antitrypanosomal activity of 5′-deoxy-5′-(iodo-methylene) adenosine and Related 6-N-cyclopropyl-adenosine analogs. J. Med. Chem. 2006, 49, 2096-2102.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 2096-2102
-
-
Rapp, M.1
Haubrich, T.A.2
Perrault, J.3
MacKey, Z.B.4
McKerrow, J.H.5
-
10
-
-
43049129233
-
S-Ribosylhomocysteine analogues with the carbon-5 and sulfur atoms replaced by a vinyl or (fluoro)vinyl unit. Bioorg
-
Wnuk, S.F.; Lalama, J.; Garmendia, C.A.; Robert, J.; Zhu, J.; Pei, D. S-Ribosylhomocysteine analogues with the carbon-5 and sulfur atoms replaced by a vinyl or (fluoro)vinyl unit. Bioorg. Med. Chem. 2008, 16, 5090-5102.
-
(2008)
Med. Chem.
, vol.16
, pp. 5090-5102
-
-
Wnuk, S.F.1
Lalama, J.2
Garmendia, C.A.3
Robert, J.4
Zhu, J.5
Pei, D.6
-
11
-
-
33644904620
-
Recent advances in fluorinated vinylstannanes and their synthetic utility
-
Shen, Y. Recent advances in fluorinated vinylstannanes and their synthetic utility. J. Organomet. Chem. 2006, 691, 1452-1461.
-
(2006)
J. Organomet. Chem.
, vol.691
, pp. 1452-1461
-
-
Shen, Y.1
-
12
-
-
0026022047
-
Nucleic acid related compounds. 63. Synthesis of 5′-deoxy-5′- methyleneadenosine and related Wittig-extended nucleosides
-
Wnuk, S.F.; Robins, M.J. Nucleic acid related compounds. 63. Synthesis of 5′-deoxy-5′- methyleneadenosine and related Wittig-extended nucleosides. Can. J. Chem. 1991, 69, 334-338.
-
(1991)
Can. J. Chem.
, vol.69
, pp. 334-338
-
-
Wnuk, S.F.1
Robins, M.J.2
-
13
-
-
0026347362
-
Nucleic acid related compounds. 67. Synthesis of 5′-amino and 5′-methylthio chain-extended nucleosides from uridine
-
Wnuk, S.F.; Dalley, N.K.; Robins, M.J. Nucleic acid related compounds. 67. Synthesis of 5′-amino and 5′-methylthio chain-extended nucleosides from uridine. Can. J. Chem. 1991, 69, 2104-2111.
-
(1991)
Can. J. Chem.
, vol.69
, pp. 2104-2111
-
-
Wnuk, S.F.1
Dalley, N.K.2
Robins, M.J.3
-
14
-
-
40849141834
-
Vinyl sulfone-modified carbohydrates: An inconspicuous group of chiral building blocks
-
Pathak, T. Vinyl sulfone-modified carbohydrates: an inconspicuous group of chiral building blocks. Tetrahedron 2008, 64, 3605-3628.
-
(2008)
Tetrahedron
, vol.64
, pp. 3605-3628
-
-
Pathak, T.1
-
15
-
-
0346731108
-
Sulfur extrusion with tin radical: Synthesis of 4′,5′- didehydro- 5′-deoxy-5′-(tributylstannyl)adenosine, an intermediate for potential inhibitors against S-adenosyl homocysteine hydrolase
-
Kumamoto, H.; Onuma, S.; Tanaka, H. Sulfur extrusion with tin radical: Synthesis of 4′,5′-didehydro- 5′-deoxy-5′- (tributylstannyl)adenosine, an intermediate for potential inhibitors against S-adenosyl homocysteine hydrolase. J. Org. Chem. 2004, 69, 72-78.
-
(2004)
J. Org. Chem.
, vol.69
, pp. 72-78
-
-
Kumamoto, H.1
Onuma, S.2
Tanaka, H.3
-
16
-
-
2942568530
-
Synthesis of quaternary amino acids bearing a (2′Z)- fluorovinyl α-branch: Potential PLP enzyme inactivators
-
Berkowitz, D.B.; DelaSalud-Bea, R.; Jahng, W.J. Synthesis of quaternary amino acids bearing a (2′Z)- fluorovinyl α-branch: Potential PLP enzyme inactivators. Org. Lett. 2004, 6, 1821-1824.
-
(2004)
Org. Lett.
, vol.6
, pp. 1821-1824
-
-
Berkowitz, D.B.1
Delasalud-Bea, R.2
Jahng, W.J.3
-
17
-
-
33846225672
-
Examination of the new α-(2′Zfluoro) vinyl trigger with lysine decarboxylase: The absolute stereochemistry dictates the reaction course
-
Karukurichi, K.R.; DelaSalud-Bea, R.; Jahng, W.J.; Berkowitz, D.B. Examination of the new α-(2′Zfluoro) vinyl trigger with lysine decarboxylase: The absolute stereochemistry dictates the reaction course. J. Am. Chem. Soc. 2007, 129, 258-259.
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 258-259
-
-
Karukurichi, K.R.1
Delasalud-Bea, R.2
Jahng, W.J.3
Berkowitz, D.B.4
-
18
-
-
3042828436
-
Radical-mediated silyl- and germyldesulfonylation of vinyl and (α-fluoro)vinyl sulfones: Application of tris(trimethylsilyl)silanes and tris(trimethylsilyl)germanes in Pd-catalyzed couplings
-
Wnuk, S.F.; Garcia, P.I., Jr.; Wang, Z. Radical-mediated silyl- and germyldesulfonylation of vinyl and (α-fluoro)vinyl sulfones: Application of tris(trimethylsilyl)silanes and tris(trimethylsilyl)germanes in Pd-catalyzed couplings. Org. Lett. 2004, 6, 2047-2049.
-
(2004)
Org. Lett.
, vol.6
, pp. 2047-2049
-
-
Wnuk, S.F.1
Garcia Jr., P.I.2
Wang, Z.3
-
20
-
-
84889430280
-
32Ge Biological activity of organogermanium compounds
-
Gielen, M.; Tiekink, E. R. T., Eds.
-
32Ge Biological activity of organogermanium compounds. In Metallotherapeutic Drugs and Metal-Based Diagnostic Agents, Gielen, M.; Tiekink, E. R. T., Eds. 2005; pp 279-295.
-
(2005)
Metallotherapeutic Drugs and Metal-Based Diagnostic Agents
, pp. 279-295
-
-
Lukevics, E.1
Ignatovich, L.2
-
21
-
-
0042555437
-
Biological activity of organogermanium compounds
-
Rappoport, Z., Ed.
-
Lukevics, E.; Ignatovich, L. Biological activity of organogermanium compounds. In The Chemistry of Organic Germanium, Tin and Lead Compounds, Rappoport, Z., Ed. 2002; pp 1653-1683.
-
(2002)
The Chemistry of Organic Germanium, Tin and Lead Compounds
, pp. 1653-1683
-
-
Lukevics, E.1
Ignatovich, L.2
-
22
-
-
0000016224
-
Syntheses and properties of silicon- and germanium-containing α-amino acids and peptides: A study on C/Si/Ge bioisosterism
-
Tacke, R.; Merget, M.; Bertermann, R.; Bernd, M.; Beckers, T.; Reissmann, T. Syntheses and properties of silicon- and germanium-containing α-amino acids and peptides: A study on C/Si/Ge bioisosterism. Organometallics 2000, 19, 3486-3497.
-
(2000)
Organometallics
, vol.19
, pp. 3486-3497
-
-
Tacke, R.1
Merget, M.2
Bertermann, R.3
Bernd, M.4
Beckers, T.5
Reissmann, T.6
-
24
-
-
0010870467
-
Synthesis, structure and biological activity of 6-R3Si(Ge,Sn)-substituted 5-fluorouracils
-
Lukevics, E.; Ignatovich, L.; Shilina, N.; Kemme, A.; Sjakste, N. Synthesis, structure and biological activity of 6-R3Si(Ge,Sn)-substituted 5-fluorouracils. Metal-Based Drugs 1994, 1, 65-72.
-
(1994)
Metal-Based Drugs
, vol.1
, pp. 65-72
-
-
Lukevics, E.1
Ignatovich, L.2
Shilina, N.3
Kemme, A.4
Sjakste, N.5
-
25
-
-
0022119102
-
Synthesis of anomeric 5-trimethylgermyl-2′-Deoxyuridines and study of their antiviral and cytotoxic properties
-
Mel'nik, S.l.; Bakhmedova, A.A.; Nedorezova, T.P.; Iartseva, I.V.; Zhukova, O.S.; et al. Synthesis of anomeric 5-trimethylgermyl-2′- Deoxyuridines and study of their antiviral and cytotoxic properties. Bioorg. Khim. 1985, 11, 1248-1252.
-
(1985)
Bioorg. Khim.
, vol.11
, pp. 1248-1252
-
-
Mel'Nik, S.L.1
Bakhmedova, A.A.2
Nedorezova, T.P.3
Iartseva, I.V.4
Zhukova, O.S.5
-
26
-
-
46049109074
-
(Me3Si)3SiH: Twenty years after its discovery as a radical-based reducing agent
-
Chatgilialoglu, C. (Me3Si)3SiH: Twenty years after its discovery as a radical-based reducing agent. Chem. Eur. J. 2008, 14, 2310-2320.
-
(2008)
Chem. Eur. J.
, vol.14
, pp. 2310-2320
-
-
Chatgilialoglu, C.1
-
27
-
-
0001636242
-
Stereoselective synthesis of vinylgermanes and their facile transformation into vinyl halides
-
Oda, H.; Morizawa, Y.; Oshima, K.; Nozaki, H. Stereoselective synthesis of vinylgermanes and their facile transformation into vinyl halides. Tetrahedron Lett. 1984, 25, 3221-3224.
-
(1984)
Tetrahedron Lett.
, vol.25
, pp. 3221-3224
-
-
Oda, H.1
Morizawa, Y.2
Oshima, K.3
Nozaki, H.4
-
28
-
-
28244439903
-
Trans- and cis-selective Lewis acid catalyzed hydrogermylation of alkynes
-
Schwier, T.; Gevorgyan, V. Trans- and cis-selective Lewis acid catalyzed hydrogermylation of alkynes. Org. Lett. 2005, 7, 5191-5194.
-
(2005)
Org. Lett.
, vol.7
, pp. 5191-5194
-
-
Schwier, T.1
Gevorgyan, V.2
-
29
-
-
28844495293
-
On the stereospecific conversion of proximallyoxygenated trisubstituted vinyltriphenylstannanes into stereodefined trisubstituted alkenes
-
Dimopoulos, P.; Athlan, A.; Manaviazar, S.; Hale, K.J. On the stereospecific conversion of proximallyoxygenated trisubstituted vinyltriphenylstannanes into stereodefined trisubstituted alkenes. Org. Lett. 2005, 7, 5373-5376.
-
(2005)
Org. Lett.
, vol.7
, pp. 5373-5376
-
-
Dimopoulos, P.1
Athlan, A.2
Manaviazar, S.3
Hale, K.J.4
-
30
-
-
0001289503
-
Bond dissociation energies in organometallic compounds
-
Basch, H. Bond dissociation energies in organometallic compounds. Inorg. Chim. Acta 1996, 252, 265-279.
-
(1996)
Inorg. Chim. Acta
, vol.252
, pp. 265-279
-
-
Basch, H.1
-
31
-
-
0033484573
-
Polarity-reversal catalysis of hydrogen-atom abstraction reactions: Concepts and applications in organic chemistry
-
Roberts, B.P. Polarity-reversal catalysis of hydrogen-atom abstraction reactions: concepts and applications in organic chemistry. Chem. Soc. Rev. 1999, 28, 25-35.
-
(1999)
Chem. Soc. Rev.
, vol.28
, pp. 25-35
-
-
Roberts, B.P.1
-
32
-
-
37249071755
-
Radical reactions in aqueous medium using (Me3Si)3SiH
-
Postigo, A.; Kopsov, S.; Ferreri, C.; Chatgilialoglu, C. Radical reactions in aqueous medium using (Me3Si)3SiH. Org. Lett. 2007, 9, 5159-5162.
-
(2007)
Org. Lett.
, vol.9
, pp. 5159-5162
-
-
Postigo, A.1
Kopsov, S.2
Ferreri, C.3
Chatgilialoglu, C.4
-
33
-
-
2142852144
-
2′ and 3′-ketonucleosides and their arabino and xylo reduction products: Convenient access via selective protection and oxidation of ribonucleosides
-
Hansske, F.; Madej, D.; Robins, M.J. 2′ and 3′- ketonucleosides and their arabino and xylo reduction products: Convenient access via selective protection and oxidation of ribonucleosides. Tetrahedron 1984, 40, 125-135.
-
(1984)
Tetrahedron
, vol.40
, pp. 125-135
-
-
Hansske, F.1
Madej, D.2
Robins, M.J.3
-
34
-
-
17444411897
-
Application of vinyl tris(trimethylsilyl)germanes in Pd-catalyzed couplings
-
Wang, Z.; Wnuk, S.F. Application of vinyl tris(trimethylsilyl)germanes in Pd-catalyzed couplings. J. Org. Chem. 2005, 70, 3281-3284.
-
(2005)
J. Org. Chem.
, vol.70
, pp. 3281-3284
-
-
Wang, Z.1
Wnuk, S.F.2
|