[(2-Deoxy- and -D-Erythro-Pentofuranosyl)Thymin-1-yl] Methane Derivatives as Potential Conformational Probes for altDNA Oligonucleotides (English)
- New search for: Scremin, C. L.
- New search for: Boal, J. H.
- New search for: Wilk, A.
- New search for: Phillips, L. R.
- New search for: Beaucage, S. L.
- New search for: Scremin, C. L.
- New search for: Boal, J. H.
- New search for: Wilk, A.
- New search for: Phillips, L. R.
- New search for: Beaucage, S. L.
In:
BIOORGANIC AND MEDICINAL CHEMISTRY LETTERS
;
6
, 2
;
207-212
;
1996
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ISSN:
- Article (Journal) / Print
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Title:[(2-Deoxy- and -D-Erythro-Pentofuranosyl)Thymin-1-yl] Methane Derivatives as Potential Conformational Probes for altDNA Oligonucleotides
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Contributors:Scremin, C. L. ( author ) / Boal, J. H. ( author ) / Wilk, A. ( author ) / Phillips, L. R. ( author ) / Beaucage, S. L. ( author )
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Published in:BIOORGANIC AND MEDICINAL CHEMISTRY LETTERS ; 6, 2 ; 207-212
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Publisher:
- New search for: PERGAMON PRESS
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Publication date:1996-01-01
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Size:6 pages
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ISSN:
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Type of media:Article (Journal)
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Type of material:Print
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Language:English
- New search for: 572.5
- Further information on Dewey Decimal Classification
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Classification:
DDC: 572.5 -
Source:
© Metadata Copyright the British Library Board and other contributors. All rights reserved.
Table of contents – Volume 6, Issue 2
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 115
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Alkylbenzyl ethers of hydroquinones as monoamine oxidase B inhibitorsArvanitis, A.G. et al. | 1996
- 121
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Syntheses and exploration of new biological activities in ethyl 6-7- substituted and 6,7-disubstituted quinolin-4-one-3-carboxylatesRoy, K. et al. | 1996
- 127
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Oximes: A new class of methoxytetrahydropyranyl inhibitors of leukotriene biosynthesis with high in vitro and in vivo potencyPlé, P.A. et al. | 1996
- 133
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Conversion of the covalent intermediate 3-fluoro-2-phospholactyl- EPTase to 3-fluoro-2-phospholactyl-UDP-GLcNAcSalleh, H.M. et al. | 1996
- 139
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Correlation of oxidation potential and toxicity in thiobenzamidesCoppola, G.M. et al. | 1996
- 143
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3-Substituted alanines inactivate a-aminobutyric acid aminotransferase by the same mechanism as do 4-amino-5-halopentanoic acid analoguesSilverman, R.B. et al. | 1996
- 143
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3-Substituted Alanines Inactivate gamma-Aminobutyric Acid Aminotransferase by the Same Mechanism as do 4-Amino-5-Halopentanoic Acid AnaloguesSilverman, R. B. / Olson, G. T. et al. | 1996
- 147
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New non-nucleosidic phosphoramidite reagent for solid phase synthesis of biotinylated oligonucleotidesNeuner, P. et al. | 1996
- 147
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New non nucleosidic CE phosphoramidite reagent for solid phase synthesis of biotinylated oligonucleotidesNeuner, P. et al. | 1996
- 153
-
Inhibitory stereochemistry of N-chloroacetyl-N-hydroxyleucine methyl ester for thermolysinKim, D.H. et al. | 1996
- 157
-
Synthesis of water-soluble prodrugs of the cytotoxic agent Combretastatin A4Bedford, S.B. et al. | 1996
- 161
-
Indolizidine derivatives as potential substance P antagonistsChan, C. et al. | 1996
- 165
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The design and synthesis of non-peptide ligands with affinity and selectivity for tachykinin receptorsHorwell, D.C. et al. | 1996
- 167
-
6N-Cinnamoyl-b-naltrexamine and its p-nitro derivative. High efficacy k-opioid agonists with weak antagonist actionsDerrick, I. et al. | 1996
- 167
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6N-Cinnamoyl--Naltrexamine and Its p-Nitro Derivative. High Efficacy kappa-Opioid Agonists with Weak Antagonist ActionsDerrick, I. / Moynihan, H. A. / Broadbear, J. / Woods, J. H. / Lewis, J. W. et al. | 1996
- 173
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Synthesis of new non-nucleoside inhibitors of HIV-1Dollé, V. et al. | 1996
- 179
-
Synthesis, enzymatic phosphorylation and antiviral activity of acyclic dienyl phosphonate derivatives of guanineNavé, J.-F. et al. | 1996
- 185
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Synthetic studies of 8-carbamoylimidazo-(5,1-d)-1,2,3,5- tetrazin-4(3H)-one: A key derivative of antitumour drug temozolomideWang, Y. et al. | 1996
- 189
-
Structure activity relationships of tetrahydrocannabinol analogues on human cannabinoid receptorsGareau, Y. et al. | 1996
- 195
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Synthesis and evaluation of pyrazolo(3,4-b)quinoline ribofuranosides and their derivatives as inhibitors of oncogenic RasWolin, R. et al. | 1996
- 201
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Synthesis and pharmacology of 2-alkyl raloxifene analogsGrese, T.A. et al. | 1996
- 207
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((2-Deoxy-a- and b-D-erythro-pentofuranosyl)thymin-1-yl) methane derivatives as potential conformational probes for altDNA oligonucleotidesScremin, C.L. et al. | 1996
- 207
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[(2-Deoxy- and -D-Erythro-Pentofuranosyl)Thymin-1-yl] Methane Derivatives as Potential Conformational Probes for altDNA OligonucleotidesScremin, C. L. / Boal, J. H. / Wilk, A. / Phillips, L. R. / Beaucage, S. L. et al. | 1996
- 213
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Synthesis of highly potent RXR-specific retinoids: The use of a cyclopropyl group as a double bond isostereVuligonda, V. et al. | 1996
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Instructions to Contributors| 1996
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Contributors to this Issue| 1996
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Graphical Abstracts| 1996