-
1
-
-
0001120760
-
Design principles for improving nucleic acid recognition by synthetic oligonucleotides
-
Kool, E.T. Preorganization of DNA: Design principles for improving nucleic acid recognition by synthetic oligonucleotides. Chem. Rev. 1997, 97, 1473-1488.
-
(1997)
Chem. Rev
, vol.97
, pp. 1473-1488
-
-
Kool, E.T.1
Preorganization of, D.N.A.2
-
2
-
-
0037179624
-
Enhancement of nucleoside cytotoxicity through nucleotide prodrugs
-
Rose, J.D.; Parker, W.B.; Someya, H.; Shaddix, S.C.; Montgomery, J.A.; Secrist, J.A., III, . Enhancement of nucleoside cytotoxicity through nucleotide prodrugs. J. Med. Chem. 2002, 45, 4505-4512.
-
(2002)
J. Med. Chem
, vol.45
, pp. 4505-4512
-
-
Rose, J.D.1
Parker, W.B.2
Someya, H.3
Shaddix, S.C.4
Montgomery, J.A.5
Secrist III, J.A.6
-
3
-
-
0036169162
-
-
Leumann, C. DNA Analogues: From supramolecular principles to biological properties. Bioorg. Med. Chem. 2002, 10, 841-854.
-
Leumann, C. DNA Analogues: From supramolecular principles to biological properties. Bioorg. Med. Chem. 2002, 10, 841-854.
-
-
-
-
4
-
-
33947092205
-
Extreme conformational flexibility of furanose ring in DNA and RNA
-
Levitt, M.; Warshel, A. Extreme conformational flexibility of furanose ring in DNA and RNA. J. Am. Chem. Soc. 1978, 100, 2607-2613.
-
(1978)
J. Am. Chem. Soc
, vol.100
, pp. 2607-2613
-
-
Levitt, M.1
Warshel, A.2
-
5
-
-
0032054586
-
HIV-1 Reverse transciptase can discriminate between two conformationally locked carbocyclic AZT triphosphate analogues
-
Marquez, V.E.; Ezzitouni, A.; Russ, P.; Siddiqui, M.A.; Ford, H.; Feldman, R.J.; Mitsuya, H.; George, C.; Barchi, J.J. HIV-1 Reverse transciptase can discriminate between two conformationally locked carbocyclic AZT triphosphate analogues. J. Am. Chem. Soc. 1998, 120, 2780-2789.
-
(1998)
J. Am. Chem. Soc
, vol.120
, pp. 2780-2789
-
-
Marquez, V.E.1
Ezzitouni, A.2
Russ, P.3
Siddiqui, M.A.4
Ford, H.5
Feldman, R.J.6
Mitsuya, H.7
George, C.8
Barchi, J.J.9
-
6
-
-
0019923858
-
How Flexible is the Furanose Ring? 1. A comparison of experimental and theoretical studies
-
Olson, W.K. How Flexible is the Furanose Ring? 1. A comparison of experimental and theoretical studies. J. Am. Chem. Soc. 1982, 104, 278-286.
-
(1982)
J. Am. Chem. Soc
, vol.104
, pp. 278-286
-
-
Olson, W.K.1
-
7
-
-
12444262177
-
New conformationally locked bicyclic N,O-nucleoside analogues of antiviral drugs
-
Procopio, A.; Alcaro, S.; De Nino, A.; Maiuolo, L.; Ortuso, F.; Sindona, G. New conformationally locked bicyclic N,O-nucleoside analogues of antiviral drugs. Bioorg. Med. Chem. Lett. 2005, 15, 545-550.
-
(2005)
Bioorg. Med. Chem. Lett
, vol.15
, pp. 545-550
-
-
Procopio, A.1
Alcaro, S.2
De Nino, A.3
Maiuolo, L.4
Ortuso, F.5
Sindona, G.6
-
8
-
-
0034607840
-
Synthesis of novel nucleosides with a fused cyclopropane ring substituted by a hydroxymethyl group
-
Lescop, C.; Huet, F. Synthesis of novel nucleosides with a fused cyclopropane ring substituted by a hydroxymethyl group. Tetrahedron 2000, 56, 2995-3003.
-
(2000)
Tetrahedron
, vol.56
, pp. 2995-3003
-
-
Lescop, C.1
Huet, F.2
-
9
-
-
33748711218
-
-
Aubin, Y.; Audran, G.; Monti, H. Conformationally locked carbocyclic nucleosides: synthesis of the 1-methyl-6-oxabicyclo[3.1.0]hexane scaffold. Synlett. 2006, 14, 2215-2219.
-
Aubin, Y.; Audran, G.; Monti, H. Conformationally locked carbocyclic nucleosides: synthesis of the 1-methyl-6-oxabicyclo[3.1.0]hexane scaffold. Synlett. 2006, 14, 2215-2219.
-
-
-
-
10
-
-
33749122260
-
Analogues of a locked nucleic acid with three-carbon 2′-4′-linkages: Synthesis by ring-closing metathesis and influence on nucleic acid duplex stability and structure
-
Albaek, N.; Peterson, M.; Nielson, P. Analogues of a locked nucleic acid with three-carbon 2′-4′-linkages: Synthesis by ring-closing metathesis and influence on nucleic acid duplex stability and structure. J. Org. Chem. 2006, 71, 7731-7740.
-
(2006)
J. Org. Chem
, vol.71
, pp. 7731-7740
-
-
Albaek, N.1
Peterson, M.2
Nielson, P.3
-
11
-
-
0031139312
-
Photodecarbonylation of chiral cyclobutanones
-
Ramnauth, J.; Lee-Ruff, E. Photodecarbonylation of chiral cyclobutanones. Can. J. Chem. 1997, 75, 518-535.
-
(1997)
Can. J. Chem
, vol.75
, pp. 518-535
-
-
Ramnauth, J.1
Lee-Ruff, E.2
-
12
-
-
33646533982
-
Halogenated ketenes. XVI. Steric control in unsymmetrical ketene-olefin cycloadditions
-
Brady, W.T.; Roe, R. Halogenated ketenes. XVI. Steric control in unsymmetrical ketene-olefin cycloadditions. J. Am. Chem. Soc. 1971, 93, 1662-1664.
-
(1971)
J. Am. Chem. Soc
, vol.93
, pp. 1662-1664
-
-
Brady, W.T.1
Roe, R.2
-
13
-
-
0035112418
-
Preparation of TADOOH, a hydroperoxide from TADDOL, and use in highly enantioface- and enantiomer-differentiating oxidations
-
Aoki, M.; Seebach, D. Preparation of TADOOH, a hydroperoxide from TADDOL, and use in highly enantioface- and enantiomer-differentiating oxidations. Helv. Chim. Acta 2001, 84, 187-207.
-
(2001)
Helv. Chim. Acta
, vol.84
, pp. 187-207
-
-
Aoki, M.1
Seebach, D.2
-
14
-
-
0027318206
-
Microbiological Transformations. 25. Enantioselective Baeyer-Villiger oxidation as a tool for the synthesis of enantiopure bicyclic furofuran and pyrofuran chirons
-
Petit, F.; Furstoss, R. Microbiological Transformations. 25. Enantioselective Baeyer-Villiger oxidation as a tool for the synthesis of enantiopure bicyclic furofuran and pyrofuran chirons. Tetrahedron Asymmetry 1993, 4, 1341-1352.
-
(1993)
Tetrahedron Asymmetry
, vol.4
, pp. 1341-1352
-
-
Petit, F.1
Furstoss, R.2
-
15
-
-
0342593711
-
Preparation of Unsaturated α,α- dichloro acid chlorides and intramolecular [2+2] cycloadditions of the α-chloroketenes reductively generated from them. Effect of double bond geometry of the cycloaddition
-
Snider, B.B.; Walner, M. Preparation of Unsaturated α,α- dichloro acid chlorides and intramolecular [2+2] cycloadditions of the α-chloroketenes reductively generated from them. Effect of double bond geometry of the cycloaddition. Tetrahedron 1989, 45, 3171-3182.
-
(1989)
Tetrahedron
, vol.45
, pp. 3171-3182
-
-
Snider, B.B.1
Walner, M.2
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