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http://hub.abes.fr/acs/periodical/jmcmar/1991/volume_34/issue_5/101021jm00109a018/authorship/1
http://hub.abes.fr/acs/periodical/joceah/1985/volume_50/issue_3/101021jo00203a017/authorship/2
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Absolute stereochemistry of palytoxin
Conformationally constrained analogs of diacylglycerol. Interaction of .gamma.-lactones with the phorbol ester receptor of protein kinase C
Conformationally Locked Nucleoside Analogs. Synthesis of Dideoxycarbocyclic Nucleoside Analogs Structurally Related to Neplanocin C
Ring expansion of ketones to 1,2-keto thioketals. Control of bond migration
Conformationally Constrained Phosphotyrosyl Mimetics Designed as Monomeric src Homology 2 Domain Inhibitors
Synthesis of carbocyclic analogs of 1-.beta.-D-psicofuranosyl nucleosides. psico-Cyclopentenyladenosine (psicoplanocin A) and psico-cyclopentenylcytosine
The effect of two antipodal fluorine-induced sugar puckers on the conformation and stability of the Dickerson-Drew dodecamer duplex [d(CGCGAATTCGCG)]2
Antitumor properties of 2(1H)-pyrimidinone riboside (zebularine) and its fluorinated analogs
Use of borate complexation in assigning relative stereochemistry of acyclic polyhydroxylated compounds
A Conformationally Locked Analogue of the Anti-HIV Agent Stavudine. AnImportant Correlation between Pseudorotation and Maximum Amplitude
Experimental and Structural Evidence that Herpes 1 Kinaseand Cellular DNA Polymerase(s) Discriminate on the Basis ofSugar Pucker
Biophysical studies of DNA modified with conformationally constrained nucleotides: comparison of 2′-exo (north) and 3′-exo (south) ‘locked’ templates
Solution Conformations of Helix-Forming β-Amino AcidHomooligomers
Diazeniumdiolate Ions as Leaving Groups in Anomeric DisplacementReactions: A Protection−Deprotection Strategy for Ionic Diazeniumdiolates
Reaction of Geldanamycin and C17-Substituted Analogues withGlutathione: Product Identifications and PharmacologicalImplications
Synthesis and characterization of oligonucleotides containing conformationally constrained bicyclo[3.1.0]hexane pseudosugar analogs
Comprehensive Structural Studies of 2′,3′-Difluorinated Nucleosides: Comparison of Theory, Solution, and Solid State
Adenosine Deaminase Prefers a Distinct Sugar Ring Conformation for Binding andCatalysis: Kinetic and Structural Studies
Structure−Activity Relationship Studies for the Peptide Portion of the Bladder Epithelial Cell Antiproliferative Factor from Interstitial Cystitis Patients
Interactions of Conformationally Biased North and South2‘-Fluoro-2‘,3‘-dideoxynucleoside 5‘-Triphosphates with the Active Site of HIV-1Reverse Transcriptase
Hydrolytic Reactivity Trends among Potential Prodrugs of the O2-Glycosylated Diazeniumdiolate Family. Targeting Nitric Oxide to Macrophages for Antileishmanial Activity
Conformational Analysis of an α3β1 Integrin-Binding Peptide from Thrombospondin-1: Implications for Antiangiogenic Drug Design
Carbohydrate-Based Drug Discovery, Volumes 1 and2 Edited by Chi-Huey Wong (Scripps Research Institute).Wiley-VCH, New York. 2003. xxxii + 459 (1) pp; xxiv + 486(2) pp. 7 × 10.5 in. $295.00. ISBN 3-527-30632-3.
Acutiphycin and 20,21-didehydroacutiphycin, new antineoplastic agents from the cyanophyte Oscillatoria acutissima
Avermectin chemistry: problems of conjugation, deconjugation, and epimerization
Chemistry and anti-HIV properties of 2'-fluoro-2',3'-dideoxyarabinofuranosylpyrimidines
The decomposition of 1-(.beta.-D-ribofuranosyl)-1,2-dihydropyrimidin-2-one (zebularine) in alkali: mechanism and products
Potential anti-AIDS drugs. Lipophilic, adenosine deaminase-activated prodrugs
Structure of malyngamide C
Avermectin chemistry. 2. A secure and flawless strategy for the final synthetic stages
The decomposition of 1-.beta.-(D-ribofuranosyl)-1,2-dihydropyrimidin-2-one (zebularine) in alkali: mechanism and products [Erratum to document cited in CA116(5):41960v]
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