Default: Organic and Biomolecular Chemistry

ISSN: 1477-0520

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Organic and Biomolecular Chemistry Q1 Unclaimed

Royal Society of Chemistry United Kingdom
Unfortunately this journal has not been claimed yet. For this reason, some information may be unavailable.

Organic and Biomolecular Chemistry is a journal indexed in SJR in Biochemistry and Organic Chemistry with an H index of 146. It has an SJR impact factor of 0,923 and it has a best quartile of Q1. It is published in English. It has an SJR impact factor of 0,923.

Organic and Biomolecular Chemistry focuses its scope in these topics and keywords: synthesis, nmr, biological, synthetic, h, regioselective, supplementary, information, application, kalkitoxin, ...

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy:

Type of publications:

Publication frecuency: -

Price

- €

Inmediate OA

0 €

Embargoed OA

- €

Non OA

Metrics

Organic and Biomolecular Chemistry

0,923

SJR Impact factor

146

H Index

1081

Total Docs (Last Year)

3592

Total Docs (3 years)

58997

Total Refs

11826

Total Cites (3 years)

3587

Citable Docs (3 years)

3,41

Cites/Doc (2 years)

54,58

Ref/Doc

Aims and Scope


synthesis, nmr, biological, synthetic, h, regioselective, supplementary, information, application, kalkitoxin, asymmetric, esi, ring, prepared, evaluation, compounds, reactions, spectra, dna, alkylationa,



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Easy synthesis of phenyl oligomers using a Ni complex

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Microwave-assisted one-pot synthesis and anti-biofilm activity of 2-amino-1H-imidazole/triazole conjugates

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Discovery of novel diarylpyrimidines as potent HIV-1 NNRTIs by investigating the chemical space of a less explored "hydrophobic channel"

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Synthesis of various sulfoforms of the trisaccharide beta-d-GlcpA-(1=>3)-beta-d-Galp-(1=>3)-beta-d-Galp-(1=>OMP) as probes for the study of the biosynthesis and sorting of proteoglycans

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A 'molecular switchboard' - covalent modifications to proteins and their impact on transcription

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Efficient resolution of 2,2'-dihydroxy-1,1'-binaphthyl by inclusion complexation with chiral N-(3-chloro-2-hydroxypropyl)-N,N,N-trimethylammonium chloride

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A 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

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Hydrogen bonding between histidine and lignin model compounds or redox mediators as calculated with the DFT method. Effects on the ease of oxidation

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Oligocyclization of 2-(hydroxymethyl)pyrroles with electron-withdrawing groups at beta-positions: formation and structural elucidation of porphyrinogens and hexaphyrinogens

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New biophysical probes for structure-activity analyses of vacuolar-H+-ATPase enzymes

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Photochromism of polymorphic 4,4'-methylenebis(N-salicylidene-2,6-diisopropylaniline) crystals

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Microwave-assisted synthesis of allylic amines: considerable rate acceleration in the hydrozirconation-transmetalation-aldimine addition sequence

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A novel and facile synthesis of dienals and substituted 2H-pyrans via the Vilsmeier reaction of a-oxo-ketenedithioacetals

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Highly sensitive and selective colorimetric and off-on fluorescent probe for Cu2+ based on rhodamine derivative

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Bio-inspired enantioselective total syntheses of (-)-viminalins A, B, H, I, and N and structural reassignment of (-)-viminalin M

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The fluorine-containing p-allylmetal complex. The transition metal-catalyzed allylic substitution reaction of fluorinated allyl mesylates with various carbon nucleophiles

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Isoprenoid biosynthesis via the MEP pathway. Synthesis of (3R,4S)-3,4-dihydroxy-5-oxohexylphosphonic acid, an isosteric analogue of 1-deoxy-d-xylulose 5-phosphate, the substrate of the 1-deoxy-d-xylulose 5-phosphate reducto-isomerase

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An 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

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Oligodeoxynucleotides containing a-l-ribo configured LNA-type C-aryl nucleotides

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Synthesis of N-acyl-N,a,a-trialkyl and N-acyl-a,a-dialkyl glycines by selective cleavage of Ugi-Passerini adducts. Qualitative assessment of the effect of substituents on the path and yield of reaction

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Atom-efficient electrophilic aromatic nitration by dinitrogen pentoxide catalysed by zirconium(iv) 2,4-pentanedionate

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Indolequinone antitumour agents: correlation between quinone structure and rate of metabolism by recombinant human NAD(P)H:quinone oxidoreductase

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Precise structure activity relationships in asymmetric catalysis using carbohydrate scaffolds to allow ready fine tuning: dialkylzinc-aldehyde additions

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