ISSN: 1381-1177

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Journal of Molecular Catalysis B: Enzymatic Q3 Unclaimed

Elsevier Netherlands

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Journal of Molecular Catalysis B: Enzymatic is a journal indexed in SJR in Biochemistry and Bioengineering with an H index of 99. It has an SJR impact factor of 0,324 and it has a best quartile of Q3. It is published in English. It has an SJR impact factor of 0,324.

Type: Journal

Type of Copyright:

Languages: English

Open Access Policy: Open Choice

Type of publications:

Publication frecuency: -

Categories: Bioengineering (Q3) Process Chemistry and Technology (Q3) Biochemistry (Q4) Catalysis (Q4)

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Metrics

Journal of Molecular Catalysis B: Enzymatic

0,324

SJR Impact factor

99

H Index

0

Total Docs (Last Year)

1

Total Docs (3 years)

0

Total Refs

3

Total Cites (3 years)

1

Citable Docs (3 years)

0

Cites/Doc (2 years)

0.0

Ref/Doc

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Aims and Scope

Best articles by citations

Site-specific mutagenesis at positions 272 and 273 of the Bacillus sp. SAM1606 a-glucosidase to screen mutants with altered specificity for oligosaccharide production by transglucosylation

Lipase catalyzed reactions of aliphatic and arylaliphatic carbonic acid esters

Molecular adaptation to cold of an Antarctic bacterial lipase

Enzymatic resolution of 2-phenyl-1-propanol by enantioselective hydrolysis of its ester having a bulky group in an acyl moiety

Lipase-catalysed ammoniolysis of lipids. A facile synthesis of fatty acid amides [J. Mol. Catal. B, 1 (1996) 109-113]

Stabilization of d-hydantoinase by intersubunit cross-linking

Immobilization of beta-galactosidase from Kluyveromyces lactis on silica and agarose: comparison of different methods

Immobilization of catalase via adsorption onto l-histidine grafted functional pHEMA based membrane

Lipase-catalyzed conversions of trimethylsilyl ethers: deprotection, acetylation, epoxidation and one-pot-multi-step reactions

Lipase-catalyzed enantioselective deacetylation of ortho-substituted phenyl acetates with 1-butanol in organic solvents

Lipase-catalyzed enantiotope selective acetylation of 2-acyloxypropane-1,3-diols. Influence of the acyl moiety on the selectivity

Enzymatic synthesis of - and sedoheptulose 7-phosphate and ido-heptulose 7-phosphate

SHOW MORE ARTICLES

New fluorescent glycerolipids for a dual wavelength assay of lipase activity and stereoselectivity

Comparative studies on the sugar esters synthesis catalysed by Candida antarctica and Candida rugosa lipases in hexane

Mass transfer limitation as a tool to enhance the enantiomeric excess in the enzymatic synthesis of chiral cyanohydrins

Lipase-catalyzed regioselective acylation of resorcin[4]arenes

Enzymatic synthesis of AHA derivatives for cosmetic application

Enzymatic synthesis of fatty acid ascorbyl esters

Oxidation of isoeugenol and coniferyl alcohol catalyzed by laccases isolated from Rhus vernicifera Stokes and Pycnoporus coccineus

Enantio-reversal in Candida rugosa lipase-catalyzed esterification of 3-hydroxybutyric acid

Enzymatic synthesis of the acrylic esters: a comparative study

Use of Mucor miehei lipase in the preparation of long chain 3-O-acylcatechins

The evolution of a non universal codon as detected in Candida rugosa lipase

Functionalization of natural drimanic compounds via microbial/chemical tandem reactions