On the public citation graph
An Efficient and Practical Synthesis of the HIV Protease Inhibitor Atazanavir via a Highly Diastereoselective Reduction Approach
0 signed · 52 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/anie.199115313openalex-snapshot
New Approaches to the Use of Amino Acids as Chiral Building Blocks in Organic Synthesis [New Synthetic Methods (85)]
inferredcites →https://doi.org/10.1016/s0040-4020(01)80651-7openalex-snapshot
Stereocontrolled Synthesis of Erythro N-Protected α-Amino Epoxides and Peptidyl Epoxides.
inferredcites →https://doi.org/10.1016/s0040-4039(00)01993-6openalex-snapshot
Diastereoselective reduction of N-phthaloyl α-amino ketones: synthesis of syn-3-amino-1,2-diol derivatives
inferredcites →https://doi.org/10.1016/s0040-4039(00)61696-9openalex-snapshot
Synthetic studies towards amino alcohols. Diastereocontrolled reduction of α′-chiral α,β-enones.
inferredcites →https://doi.org/10.1016/s0040-4039(01)81363-0openalex-snapshot
On the facile dehydrohalogenation of amino acid derived chloromethyl ketones.
inferredcites →https://doi.org/10.1016/s0040-4039(98)00897-1openalex-snapshot
A concise synthesis of aza-dipeptide isosteres
inferredcites →https://doi.org/10.1016/s0891-8422(23)00530-xopenalex-snapshot
NEW DRUGS ON THE HORIZON
inferredcites →https://doi.org/10.1021/cr050997uopenalex-snapshot
Industrial Syntheses of the Central Core Molecules of HIV Protease Inhibitors
inferredcites →https://doi.org/10.1021/jm970873copenalex-snapshot
New Aza-Dipeptide Analogues as Potent and Orally Absorbed HIV-1 Protease Inhibitors: Candidates for Clinical Development
inferredcites →https://doi.org/10.1021/jo010270fopenalex-snapshot
Highly Stereoselective Syntheses of syn- and anti-1,2-Amino Alcohols
inferredcites →https://doi.org/10.1021/jo020442oopenalex-snapshot
Diastereoselective Reduction of a Chiral N-Boc-Protected δ-Amino-α,β-unsaturated γ-Keto Ester Phe-Gly Dipeptidomimetic
inferredcites →https://doi.org/10.1021/jo970579sopenalex-snapshot
A Stereocontrolled, Convergent Synthesis of Hydroxyethylene Dipeptide Isosteres
inferredcites →https://doi.org/10.1021/op025504ropenalex-snapshot
Process Research and Development for an Efficient Synthesis of the HIV Protease Inhibitor BMS-232632
inferredcites →https://doi.org/10.1097/00126334-200301010-00004openalex-snapshot
Results of a Phase 2 Clinical Trial at 48 Weeks (AI424-007): A Dose-Ranging, Safety, and Efficacy Comparative Trial of Atazanavir at Three Doses in Combination with Didanosine and Stavudine in Antiretroviral-Naive Subjects
inferredcites →https://doi.org/10.1128/aac.00098-06openalex-snapshot
Population Pharmacokinetics of Atazanavir in Patients with Human Immunodeficiency Virus Infection
inferredcites →https://doi.org/10.1517/13543784.11.9.1295openalex-snapshot
Atazanavir: a novel HIV-1 protease inhibitor
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4767406openalex-extracted
Ultra-Small Palladium Nanoparticles Supported by Cobalt-Containing Mesoporous Carbon: Highly Efficient Magnetic Reusable Catalyst in Green Media
inferred← citeshttps://doi.org/10.1002/9780470929353.ch1openalex-snapshot
Discovery and Development of Atazanavir
inferred← citeshttps://doi.org/10.1002/adsc.200900565openalex-snapshot
Highly Efficient Synthesis of New α‐Arylamino‐α′‐chloropropan‐2‐ones via Oxidative Hydrolysis of Vinyl Chlorides Promoted by Calcium Hypochlorite
inferred← citeshttps://doi.org/10.1002/ardp.202400307openalex-snapshot
An in‐depth analysis of COVID‐19 treatment: Present situation and prospects
inferred← citeshttps://doi.org/10.1002/cmdc.202100397openalex-snapshot
Amino Acid and Peptide‐Based Antiviral Agents
inferred← citeshttps://doi.org/10.1002/open.202400279openalex-snapshot
Rapid Synthesis of anti‐1,3‐Diamino‐4‐phenylbutan‐2‐ol Building Blocks via a Three‐Component Oxyhomologation and a Two‐Component Reducing System
inferred← citeshttps://doi.org/10.1007/s40242-014-3396-4openalex-snapshot
Lewis base organocatalyzed enantioselective hydrosilylation of α-keto ketimines
inferred← citeshttps://doi.org/10.1016/b978-0-323-91817-6.00017-6openalex-snapshot
New drug discovery and development
inferred← citeshttps://doi.org/10.1016/j.antiviral.2008.05.001openalex-snapshot
A survey of the syntheses of active pharmaceutical ingredients for antiretroviral drug combinations critical to access in emerging nations
inferred← citeshttps://doi.org/10.1016/j.bioorg.2020.104488openalex-snapshot
Drug repurposing for the treatment of COVID-19: Pharmacological aspects and synthetic approaches
inferred← citeshttps://doi.org/10.1016/j.bmc.2024.117605openalex-snapshot
Medicinal chemistry perspectives on the development of piperazine-containing HIV-1 inhibitors
inferred← citeshttps://doi.org/10.1016/j.jics.2023.100936openalex-snapshot
A review on synthesis of antiviral drugs, in silico studies and their toxicity
inferred← citeshttps://doi.org/10.1016/j.procbio.2018.11.003openalex-snapshot
Coupled fermentation-bioconversion process for production of chiral α-chlorohydrin with recombinant ketoreductase
inferred← citeshttps://doi.org/10.1016/j.tetasy.2017.04.008openalex-snapshot
Asymmetric biosynthesis of intermediates of anti-HIV drugs
inferred← citeshttps://doi.org/10.1021/acs.iecr.3c00908openalex-snapshot
Scale-Up of Synthesizing 3,3-Dimethyl-2-butyl Ketone (Pinacolone) from 2-Methyl-2-butene (β-Isoamylene) and Its Kinetic Study
inferred← citeshttps://doi.org/10.1021/acs.oprd.2c00005openalex-snapshot
Large-Scale Amidations in Process Chemistry: Practical Considerations for Reagent Selection and Reaction Execution
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c02166openalex-snapshot
Ti-Catalyzed Functional Group Tolerant and Regioselective Cross Couplings of (Hetero)aryl Grignard Reagents with Halopyridines
inferred← citeshttps://doi.org/10.1021/cr100346gopenalex-snapshot
Large-Scale Applications of Transition Metal-Catalyzed Couplings for the Synthesis of Pharmaceuticals
inferred← citeshttps://doi.org/10.1021/jo8007644openalex-snapshot
Copper(I)-Promoted Synthesis of Chloromethyl Ketones from Trichloromethyl Carbinols
inferred← citeshttps://doi.org/10.1021/op2003826openalex-snapshot
Large-Scale Carbonyl Reductions in the Pharmaceutical Industry
inferred← citeshttps://doi.org/10.1021/op500305sopenalex-snapshot
Large-Scale Applications of Amide Coupling Reagents for the Synthesis of Pharmaceuticals
inferred← citeshttps://doi.org/10.1039/c3ob41464gopenalex-snapshot
A three step continuous flow synthesis of the biaryl unit of the HIV protease inhibitorAtazanavir
inferred← citeshttps://doi.org/10.1039/d0re00118jopenalex-snapshot
Calixarene-supported Pd–NHC complexes as efficient catalysts for scalable Suzuki–Miyaura cross-couplings
inferred← citeshttps://doi.org/10.1039/d2gc04607eopenalex-snapshot
Developing a transition-metal-free green protocol for the electrophilic hydrazination of silyl enol ethers using diazo electrophiles with EtOH–H 2 O as a safe solvent
inferred← citeshttps://doi.org/10.1039/d3ob00452jopenalex-snapshot
A one-step base-free synthesis of N -arylamides via modified pivaloyl mixed anhydride mediated amide coupling
inferred← citeshttps://doi.org/10.1039/d6gc01375aopenalex-snapshot
Heterogeneous photocatalytic divergent bifunctionalization of unactivated β-bromoethylarenes via base-controlled selectivity
inferred← citeshttps://doi.org/10.11606/d.60.2016.tde-17122015-114314openalex-snapshot
Síntese, avaliação antipirética e metabolismo in vitro do propacetamol
inferred← citeshttps://doi.org/10.2174/1385272825666210706151631openalex-snapshot
Reduction of Oximes and Hydrazones: Asymmetric and Diastereoselective Approaches
inferred← citeshttps://doi.org/10.2174/1389557523666230707151553openalex-snapshot
Synthetic and Clinical Perspectives of Evotaz: An Overview
inferred← citeshttps://doi.org/10.2174/1570162x21666230522123631openalex-snapshot
A Combination of Novel HIV-1 Protease Inhibitor and Cytochrome P450 (CYP) Enzyme Inhibitor to Explore the Future Prospective of Antiviral Agents: Evotaz
inferred← citeshttps://doi.org/10.3390/catal10091081openalex-snapshot
Palladium PEPPSI-IPr Complex Supported on a Calix[8]arene: A New Catalyst for Efficient Suzuki–Miyaura Coupling of Aryl Chlorides
inferred← citeshttps://doi.org/10.3390/molecules20059229openalex-snapshot
Synthesis and Biological Evaluation of Hydrazone Derivatives as Antifungal Agents
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.