ISSN: 1477-0520

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Organic and Biomolecular Chemistry Q2 Unclaimed

Royal Society of Chemistry United Kingdom

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Organic and Biomolecular Chemistry is a journal indexed in SJR in Biochemistry and Organic Chemistry with an H index of 184. It has an SJR impact factor of 0,607 and it has a best quartile of Q2. It is published in English. It has an SJR impact factor of 0,607.

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: -

Categories: Organic Chemistry (Q2) Physical and Theoretical Chemistry (Q2) Biochemistry (Q3)

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Non OA

Metrics

0,607

SJR Impact factor

184

H Index

1052

Total Docs (Last Year)

3163

Total Docs (3 years)

57711

Total Refs

9326

Total Cites (3 years)

3156

Citable Docs (3 years)

2.88

Cites/Doc (2 years)

54.86

Ref/Doc

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Aims and Scope

Best articles by citations

Synthesis of unprotected and borane-protected cyclic phosphines using Ru? and Mo? based olefin metathesis catalystsThis 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

Easy synthesis of phenyl oligomers using a Ni complex

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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