Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry is a journal indexed in SJR in Biochemistry and Organic Chemistry with an H index of 189. It has an SJR impact factor of 0,6 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 0,6.
Organic and Biomolecular Chemistry focuses its scope in these topics and keywords: synthesis, biological, nmr, synthetic, h, supplementary, dna, asymmetric, esi, compounds, ...
Metrics
Scimago and CountryOfPapers database fields
SJR Impact
0,6
H-index
189
Docs (year)
1048
Docs 3y
3248
Total refs
58516
Cites 3y
9738
Citable 3y
3241
Cites/Doc 2y
2.84
Ref/Doc
55.84
Immediate OA
—
Embargoed OA
0 €
Non OA / Submission
—
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Best articles by citations
Bio-inspired enantioselective total syntheses of (-)-viminalins A, B, H, I, and N and structural reassignment of (-)-viminalin M
View moreTributylgermanium hydride as a replacement for tributyltin hydride in radical reactionsElectronic supplementary information (ESI) available: full experimental details and data. See http://www.rsc.org/suppdata/ob/b3/b310520b/
View moreEfficient resolution of 2,2'-dihydroxy-1,1'-binaphthyl by inclusion complexation with chiral N-(3-chloro-2-hydroxypropyl)-N,N,N-trimethylammonium chloride
View moreEasy synthesis of phenyl oligomers using a Ni complex
View moreDNA-catalyzed reactivity of a phosphoramidate functional group and formation of an unusual pyrophosphoramidate linkage
View moreDiscovery of novel diarylpyrimidines as potent HIV-1 NNRTIs by investigating the chemical space of a less explored "hydrophobic channel"
View moreDiamagnetic and paramagnetic ring currents in expanded porphyrins
View moreDevelopment of a new rhodamine-based FRET platform and its application as a Cu2+ probe
View moreDetection of a metallo-beta-lactamase (IMP-1) by fluorescent probes having dansyl and thiol groups
View moreCyclic PNA-based compound directed against HIV-1 TAR RNA: modelling, liquid-phase synthesis and TAR bindingElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/ob/b3/b311775h/
View moreControl of diastereoselectivity in the crotylation and cinnamylation of aldehydes by the selection of ligands on allylic indium reagents
View moreClostrindolin is an antimycobacterial pyrone alkaloid from Clostridium beijerinckii
View moreBiomimetic total synthesis of forbesione and desoxymorellin utilizing a tandem Claisen/Diels-Alder/Claisen rearrangement
View more3,3-Diethyl- and 3,3-dibenzyl-1,2-diferrocenylcyclopropenes
View moreBifurcated, modular syntheses of chiral annulet triazacyclononanes
View moreBend ribbon-forming tetrahydrofuran amino acidsThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years of organic chemistry research in that building, as all its current aca
View moreAtom-efficient electrophilic aromatic nitration by dinitrogen pentoxide catalysed by zirconium(iv) 2,4-pentanedionate
View moreAsymmetric synthesis of (1R,2S,3R)-3-methylcispentacin and (1S,2S,3R)-3-methyltranspentacin by kinetic resolution of tert-butyl (±)-3-methylcyclopentene-1-carboxylate
View moreApplication of Fmoc-amino acid carrying an unmasked carbohydrate to the synthesis of the epidermal growth factor-like domain of bovine blood coagulation factor IXElectronic supplementary information (ESI) available: experimental details. See http://w
View moreAn approach to the generation of simple analogues of the antitumour agent spicamycinThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years of organic chemistry research in
View moreAminocyclopentanols as sugar mimics. Synthesis from unsaturated bicyclic lactones by Overman rearrangement
View moreAbsolute stereochemistry of dihydrofuroangelicins bearing C-8 substituted double bonds: a combined chemical/exciton chirality protocolElectronic supplementary information (ESI) available: Relative energies and relevant geometrical parameters of DFT-o
View moreA novel and facile synthesis of dienals and substituted 2H-pyrans via the Vilsmeier reaction of a-oxo-ketenedithioacetals
View moreA multicomponent coupling strategy suitable for the synthesis of the triene component of the oxazolomycin antibioticsThis is one of a number of contributions from the current members of the Dyson Perrins Laboratory to mark the end of almost 90 years
View more