On the public citation graph
Some Aspects of the Chemistry of Nitro Compounds
0 signed · 101 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known work and none has been retracted — and get a dated CiteStamped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/10.1002/0471224480openalex-snapshot
The Nitro Group in Organic Synthesis
inferredcites →https://doi.org/10.1002/anie.201000723openalex-snapshot
Isocyanides in the Synthesis of Nitrogen Heterocycles
inferredcites →https://doi.org/10.1002/anie.201107601openalex-snapshot
Direct Titanium‐Mediated Conversion of Ketones into Enamides with Ammonia and Acetic Anhydride
inferredcites →https://doi.org/10.1002/cber.19190520830openalex-snapshot
Über eine eigenartige Umlagerung des Methyl‐allyl‐anilin‐ N ‐oxyds
inferredcites →https://doi.org/10.1002/cber.19220550232openalex-snapshot
Über das Verhalten von Allyl‐ und Benzyl‐aminoxyden gegen Natronlauge
inferredcites →https://doi.org/10.1002/chem.200901433openalex-snapshot
Michael Addition Initiated Carbocyclization Sequences with Nitroolefins for the Stereoselective Synthesis of Functionalized Heterocyclic and Carbocyclic Systems
inferredcites →https://doi.org/10.1016/0005-2760(78)90213-8openalex-snapshot
Bioconversion of sitosterol to useful steroidal intermediates by mutants of Mycobacterium fortuitum
inferredcites →https://doi.org/10.1016/0040-4020(94)01034-wopenalex-snapshot
A short total synthesis of estrone derivatives: A novel 1,3-rearrangement of an allylic nitro group
inferredcites →https://doi.org/10.1016/0040-4039(84)80111-2openalex-snapshot
A mild reduction of aliphatic nitro compounds to imines for further reactions : A simple synthesis of pyrroles
inferredcites →https://doi.org/10.1016/0040-4039(95)00522-eopenalex-snapshot
On the mechanism of the nitrous acid induced conversion of an isopropylidene group into an alkyne
inferredcites →https://doi.org/10.1016/0040-4039(95)01146-9openalex-snapshot
An Efficient Synthesis of Large Ring Acetylenes
inferredcites →https://doi.org/10.1016/0040-4039(96)00078-0openalex-snapshot
A new selective reduction of nitroalkenes into enamides
inferredcites →https://doi.org/10.1016/j.tet.2011.09.103openalex-snapshot
A flexible approach to hexahydronaphthalene-1-carboxylates
inferredcites →https://doi.org/10.1016/s0040-4020(01)80849-8openalex-snapshot
Iminyl radicals: Part I. generation and intramolecular capture by an olefin.
inferredcites →https://doi.org/10.1016/s0040-4020(01)80850-4openalex-snapshot
Iminyl radicals: part II. ring opening of cyclobutyl- and cyclopentyliminyl radicals.
inferredcites →https://doi.org/10.1016/s0040-4020(01)89069-4openalex-snapshot
A useful synthesis of pyrroles from nitroolefins
inferredcites →https://doi.org/10.1016/s0040-4039(00)60462-8openalex-snapshot
1,3-Rearrangement of allylic sulphones: Rearrangement-cyclisation of allylic 4-pentenyl sulphones
inferredcites →https://doi.org/10.1016/s0040-4039(00)60463-xopenalex-snapshot
Free radical rearrangement of unsaturated sulphones involving an intramolecular hydrogen abstraction
inferredcites →https://doi.org/10.1016/s0040-4039(00)61237-6openalex-snapshot
Concise enantiospecific syntheses of (+)-Eldanolide and (−)-cis-whisky lactone
inferredcites →https://doi.org/10.1016/s0040-4039(00)74843-xopenalex-snapshot
An expedient total synthesis of (±)-estrone derivatives
inferredcites →https://doi.org/10.1016/s0040-4039(00)77482-xopenalex-snapshot
A new synthesis of substituted dienes by reductive elimination of allylic nitro derivatives
inferredcites →https://doi.org/10.1016/s0040-4039(00)83993-3openalex-snapshot
Ethylidyne alkynes from isopropylidene olefins
inferredcites →https://doi.org/10.1016/s0040-4039(00)88403-8openalex-snapshot
A mild oxidative nef reaction
inferredcites →https://doi.org/10.1016/s0040-4039(00)88507-xopenalex-snapshot
A practical access to allylic sulphones and lactones from allylic nitro compounds
inferredcites →https://doi.org/10.1016/s0040-4039(00)92375-xopenalex-snapshot
A new practical method for the synthesis of acetylenes.
inferredcites →https://doi.org/10.1016/s0040-4039(00)94340-5openalex-snapshot
Cyclisation of imine radicals derived from sulphenylimines: A simple access to Δ1-pyrrolines.
inferredcites →https://doi.org/10.1016/s0040-4039(00)94438-1openalex-snapshot
Multiple radical additions starting with iminyl radicals derived from sulphenylimines.
inferredcites →https://doi.org/10.1016/s0040-4039(00)96659-0openalex-snapshot
Mechanism of the nitrous acid-induced dealkylation of trisubstituted (terminal isopropylidene) olefins to form acetylenes
inferredcites →https://doi.org/10.1016/s0040-4039(96)02015-1openalex-snapshot
A convergent approach to functionalised alkynes
inferredcites →https://doi.org/10.1016/s1460-1567(02)x8001-5openalex-snapshot
Organic Syntheses Based on Name Reactions
inferredcites →https://doi.org/10.1021/ar50077a004openalex-snapshot
Allylic sulfoxides. Useful intermediates in organic synthesis
inferredcites →https://doi.org/10.1021/cr900411fopenalex-snapshot
Isocyanoacetate Derivatives: Synthesis, Reactivity, and Application
inferredcites →https://doi.org/10.1021/ja00003a057openalex-snapshot
Ring opening induced by iminyl radicals derived from cyclobutanones: new aspects of tin hydride cleavage of S-phenyl sulfenylimines
inferredcites →https://doi.org/10.1021/ja00748a075openalex-snapshot
Reversible 1,3 transposition of sulfoxide and alcohol functions. Potential synthetic utility
inferredcites →https://doi.org/10.1021/ja00965a048openalex-snapshot
Mechanisms of Thermal Racemization of Sulfoxides1
inferredcites →https://doi.org/10.1021/ja01020a021openalex-snapshot
Thermal racemization of allylic sulfoxides and interconversion of allylic sulfoxides and sulfenates. Mechanism and stereochemistry
inferredcites →https://doi.org/10.1021/ja01239a040openalex-snapshot
Rearrangement of Allyl Groups in Dyad Systems. Amine Oxides
inferredcites →https://doi.org/10.1021/jo00364a013openalex-snapshot
Direct conversion of terpenylalkanolamines to ethylidyne N-nitroso compounds
inferredcites →https://doi.org/10.1021/jo00373a007openalex-snapshot
Facile synthesis of allylic nitro compounds by N,N-dimethylethylenediamine-catalyzed condensation of aliphatic and alicyclic ketones with primary nitroalkanes
inferredcites →https://doi.org/10.1021/jo900045kopenalex-snapshot
Expeditious Construction of (+)-Mintlactone via Intramolecular Hetero-Pauson−Khand Reaction
inferredcites →https://doi.org/10.1021/jo902259uopenalex-snapshot
A Facile and Practical Synthesis of N-Acetyl Enamides
inferredcites →https://doi.org/10.1021/jo9809332openalex-snapshot
A Three-Step Procedure for Asymmetric Catalytic Reductive Amidation of Ketones
inferredcites →https://doi.org/10.1021/jo981590aopenalex-snapshot
Practical Syntheses of β-Amino Alcohols via Asymmetric Catalytic Hydrogenation
inferredcites →https://doi.org/10.1021/ol035027copenalex-snapshot
β-Nitro Xanthates as Olefin Precursors
inferredcites →https://doi.org/10.1021/ol047472topenalex-snapshot
Mercuric Triflate-Catalyzed Tandem Cyclization Leading to Polycarbocycles
inferredcites →https://doi.org/10.1021/ol051196gopenalex-snapshot
On the [2,3] Sigmatropic Rearrangement of Allylic Nitro Compounds
inferredcites →https://doi.org/10.1021/ol902472ropenalex-snapshot
Unusual Approach to Branched 3-Alkynylamides and to 1,5-Dihydropyrrol-2-ones
inferredcites →https://doi.org/10.1039/b101751iopenalex-snapshot
Synthetic equivalents of alkynyl and propargyl radicals
inferredcites →https://doi.org/10.1039/b203383fopenalex-snapshot
New syntheses of alkynes: a tale of serendipity and design
inferredcites →https://doi.org/10.1039/b613443mopenalex-snapshot
Recent progress in the generation and use of nitrogen-centred radicals
inferredcites →https://doi.org/10.1039/c29710001001openalex-snapshot
Synthesis of 1,2,3-triazoles by reaction of azide ion with αβ-unsaturated nitro-compounds and nitriles
inferredcites →https://doi.org/10.1039/c39810000774openalex-snapshot
Efficient synthesis of the corticosteroid side-chain from 17-ketones
inferredcites →https://doi.org/10.1039/c39820000551openalex-snapshot
A simple construction of the hydroxy-ketone side chain of corticosteroids from 17-oxo-steroids via nitro-olefins
inferredcites →https://doi.org/10.1039/c39840000337openalex-snapshot
A mild and efficient method for the reduction of oximes to imines for futher in situ reactions
inferredcites →https://doi.org/10.1039/c39850001098openalex-snapshot
A new synthesis of pyrroles from nitroalkenes
inferredcites →https://doi.org/10.1039/c39850001222openalex-snapshot
Nitrosative elimination of terpenyl alkanolamines leading to alkynyl N-nitroso-analogues
inferredcites →https://doi.org/10.1039/c39890001006openalex-snapshot
A novel thermal rearrangement of allylic nitro derivatives into allylic alcohols
inferredcites →https://doi.org/10.1039/p19850002191openalex-snapshot
A further synthesis of the corticosteroid side chain starting with a suitable 17-ketone
inferredcites →https://doi.org/10.1039/p19860002243openalex-snapshot
Reduction of oximes and aliphatic nitro compounds to imines for further in situ reactions: a novel synthesis of pyrroles and pyrrolin-2-ones
inferredcites →https://doi.org/10.1039/p19870002707openalex-snapshot
1,3-Rearrangements of some allylic sulphones
inferredcites →https://doi.org/10.1039/p19890000313openalex-snapshot
Radical induced cyclisations of some cyclic unsaturated allylic sulphones
inferredcites →https://doi.org/10.1039/p19890000319openalex-snapshot
Radical induced 1,3-rearrangement–cyclisations of some unsaturated allylic sulphones
inferredcites →https://doi.org/10.1055/s-1996-5698openalex-snapshot
Iminyl Radicals: A Fresh Look at a Forgotten Species (and Some of its Relatives)
inferredcites →https://doi.org/10.1055/s-2005-918463openalex-snapshot
The Synthesis of 1,2,3-Triazoles from Nitroalkenes - Revisited
inferredcites →https://doi.org/10.1055/s-2008-1032135openalex-snapshot
(4E,8Z)-12-Methyloxacyclotetradeca-4,8-dien-2-one and Its 7a-Homologue: Conformationally Constrained Double-Unsaturated Macrocyclic Musks by Ring-Closing Alkyne Metathesis
inferredcites →https://doi.org/10.1128/aem.23.1.72-77.1972openalex-snapshot
Microbial Degradation of Sterols
inferredcites →https://doi.org/10.2533/chimia.1979.1openalex-snapshot
Nitroaliphatic Compounds - Ideal Intermediates in Organic Synthesis?
inferredcites →https://doi.org/10.3987/rev-07-622openalex-snapshot
Barton-Zard Pyrrole Synthesis and Its Application to Synthesis of Porphyrins, Polypyrroles, and Dipyrromethene Dyes
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.4187022openalex-extracted
Meanderings of a Curious Chemist
inferred← citeshttps://doi.org/10.1002/adsc.201801439openalex-snapshot
Synthesis of Functionalized Cyclobutane‐Fused Naphthalene Derivatives via Cascade Reactions of Allenynes with tert‐Butyl Nitrite
inferred← citeshttps://doi.org/10.1002/adsc.202001344openalex-snapshot
Synthesis of Nitro Alcohols by Riboflavin Promoted Tandem Nef‐Henry Reactions on Nitroalkanes
inferred← citeshttps://doi.org/10.1002/bkcs.10577openalex-snapshot
Synthesis of 1,3,4‐Trisubstituted Benzenes from Morita–Baylis–Hillman Adducts of α‐Bromocinnamaldehyde via [5+1] Annulation Strategy
inferred← citeshttps://doi.org/10.1002/chem.201903526openalex-snapshot
Straightforward Access to the Nitric Oxide Donor Azasydnone Scaffold by Cascade Reactions of Amines
inferred← citeshttps://doi.org/10.1002/chin.201303213openalex-snapshot
ChemInform Abstract: Some Aspects of the Chemistry of Nitro Compounds
inferred← citeshttps://doi.org/10.1002/cplu.202000364openalex-snapshot
High‐Pressure‐Mediated Thiourea‐Organocatalyzed Asymmetric Michael Addition to (Hetero)aromatic Nitroolefins: Prediction of Reaction Parameters by PCP‐SAFT Modelling
inferred← citeshttps://doi.org/10.1007/s10593-022-03120-8openalex-snapshot
The features of the Michael reaction in ([1,2,4]triazolo[4,3-a][1,3,5]triazin-5-yl)dinitromethanides
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00214-7openalex-snapshot
2.13 The Henry (Nitroaldol) Reaction
inferred← citeshttps://doi.org/10.1016/b978-0-323-96025-0.00111-3openalex-snapshot
The Henry (Nitroaldol) Reaction
inferred← citeshttps://doi.org/10.1016/j.cbi.2020.109229openalex-snapshot
Targeting cell cycle by β-carboline alkaloids in vitro: Novel therapeutic prospects for the treatment of cancer
inferred← citeshttps://doi.org/10.1016/j.mencom.2015.03.001openalex-snapshot
Organic and hybrid molecular systems
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00578openalex-snapshot
Radical Nitration-Debromination of α-Bromo-α-fluoroalkenes as a Stereoselective Route to Aromatic α-Fluoronitroalkenes—Functionalized Fluorinated Building Blocks for Organic Synthesis
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00040openalex-snapshot
Copper-Assisted Direct Nitration of Cyclic Ketones with Ceric Ammonium Nitrate for the Synthesis of Tertiary α-Nitro-α-substituted Scaffolds
inferred← citeshttps://doi.org/10.1039/c8cc08920eopenalex-snapshot
Transition-metal-free α-arylation of nitroketones with diaryliodonium salts for the synthesis of tertiary α-aryl, α-nitro ketones
inferred← citeshttps://doi.org/10.1039/c9cc05963fopenalex-snapshot
Selective synthesis of β-nitrated N-heterocycles and N -nitroso-2-alkoxyamine aldehydes from inactivated cyclic amines promoted by t BuONO and oxoammonium salt
inferred← citeshttps://doi.org/10.1039/c9ob01005jopenalex-snapshot
Tandem double acylation/[3,3]-rearrangement of aliphatic nitro compounds: a route to α-oxygenated oxime derivatives
inferred← citeshttps://doi.org/10.1039/d2qo00992gopenalex-snapshot
Fe-catalyzed denitrative cyanoalkylation of nitroalkenes with cycloketone oxime esters via reductive C–C bond formation
inferred← citeshttps://doi.org/10.1039/d5ra05815eopenalex-snapshot
Direct vicinal halo-nitration of unsaturated compounds: an overview
inferred← citeshttps://doi.org/10.1055/sos-sd-113-00177openalex-snapshot
13.13.6 1,2,3-Triazoles (Update 2015)
inferred← citeshttps://doi.org/10.1080/00397911.2020.1752730openalex-snapshot
Transition-metal-free mono- or dinitration of protected anilines
inferred← citeshttps://doi.org/10.1177/17475198221088194openalex-snapshot
The xanthate route to six-membered carbocycles
inferred← citeshttps://doi.org/10.1515/hc-2016-0003openalex-snapshot
Stereoselective Michael addition of O -nucleophiles to carbohydrate-based nitro-olefin
inferred← citeshttps://doi.org/10.2174/1385272823666190820113718openalex-snapshot
Comprehension of the α-Arylation of Nitroalkanes
inferred← citeshttps://doi.org/10.3389/fchem.2014.00020openalex-snapshot
Cancer wars: natural products strike back
inferred← citeshttps://doi.org/10.3390/biomedicines11102698openalex-snapshot
Steroids Bearing Heteroatom as Potential Drugs for Medicine
inferred← citeshttps://doi.org/10.3390/molecules25153390openalex-snapshot
Denitrative Cross-Couplings of Nitrostyrenes
inferred← citeshttps://doi.org/10.3390/molecules28020686openalex-snapshot
Interrupted Nef and Meyer Reactions: A Growing Point for Diversity-Oriented Synthesis Based on Nitro Compounds
inferred← citeshttps://doi.org/10.3390/molecules30183768openalex-snapshot
Analysis of the Reactivity of Z-2-Ar-1-EWG-1-Nitroethene Molecular Segment in the Hetero Diels–Alder Reaction: Experimental and MEDT Quantum Chemical Study
inferred← citeshttps://doi.org/10.70675/7c36bc77zbcf8z4d6ez988dzdd814ec9a952openalex-snapshot
Role of the immune receptor CD47 in mouse model of non-infectious uveitis
inferred← citeshttps://doi.org/10.70675/7d68b550za64ez450ez9652z105c70164939openalex-snapshot
Development of new approaches for the synthesis of flavaglines
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.