Relevant bibliographies by topics / Alicyclic compounds – Synthesis ; Microbiology

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Academic literature on the topic 'Alicyclic compounds – Synthesis ; Microbiology'

Author: Grafiati
Published: 4 June 2021
Last updated: 7 February 2022

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Journal articles on the topic "Alicyclic compounds – Synthesis ; Microbiology"

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Grygorenko, Oleksandr, Andriy Sokolov, Sergey Golovach та ін. "Diastereoselective Synthesis of Cyclic sp3-Enriched cis-β-Alkoxysulfonyl Chlorides". Synthesis 51, № 04 (2018): 848–58. http://dx.doi.org/10.1055/s-0037-1611277.

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A three-step synthesis of β-alkoxy-substituted alicyclic sulfonyl chlorides from cyclic alkenes and alcohols is reported. The scope of the method was studied for a range of the substrates with various steric and electronic properties. The title compounds were obtained on a hundred-gram scale in up to 52% overall yield scale as single cis-diastereomers.
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Mohammed, Hamid Hashim. "Synthesis of fused cyclic chromene and alicyclic chromene derivatives from 2-amino-4-[4-(dimethylamino)phenyl]5-oxo-4H,5H-pyrano [3,2-c]chromene-3-carbonitrile." Al-Mustansiriyah Journal of Science 27, no. 5 (2017): 36. http://dx.doi.org/10.23851/mjs.v27i5.165.

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Derivatives of fused cyclic chromene and alicyclic chromene were synthesized starting from 2-amino-4-[4-(dimethylamino)phenyl]5-oxo-4H,5H-pyrano [3,2-c]chromene-3-carbonitrile. The structures of the synthesized compounds were elucidated by spectral data : infrared spectra (FT-IR) and 1HNMR.
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3

Zaidi, Sadaf, Devdutt Chaturvedi, Mridula Saxena та Richa Srivastava. "Synthesis and Antimicrobial Activity of Dithiocarbamates of ω-Substituted (2-naphthyloxy)alkanes". Asian Journal of Chemistry 31, № 10 (2019): 2201–10. http://dx.doi.org/10.14233/ajchem.2019.22090.

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A series of dithiocarbamates of ω-substituted (2-naphthyloxy) alkanes was developed through condensation of 2-(2-chloro-alkoxy)-naphthalene to various kinds of aliphatic, aromatic, alicyclic, heterocyclic primary and secondary amines employing benzyl trimethyl ammonium hydroxide in catalytic quantity (Triton-B/CS2 system) afforded desired products in high yields (82-98 %). The complete series of synthesized compounds (4-48) were evaluated for antimicrobial activity through microdilution method using various bacterial and fungal strains. The antifungal and antibacterial values were estimated as
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Direnko, Dmitriy Yurievich, Boris Ivanovich Drevko, and Yaroslav Borisovich Drevko. "The Synthesis of New Selenium-containing Heterocycles by the Oxidation Reaction of 2,4-Diaryltetrahydro-4H-selenochromenes." Current Organic Chemistry 24, no. 15 (2020): 1663–68. http://dx.doi.org/10.2174/1385272824999200720165656.

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We have explored the reactions of tetrahydro-4H-selenochromenes in the presence of phosphoric pentachloride, and synthesized new condensate aroylbenzoselenophenes. During the reactions, tetrahydro-4H-selenochromenes with phosphoric pentachloride underwent oxidative aromatization and nucleophilic substitution for a chlorine atom of one of the protons in the alicyclic fragment. Also, the narrowing of the heterocyclic fragment occurred as in synthesized selenium-containing compounds earlier transformed into the corresponding condensate aroylbenzoselenophenes.
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5

Alrubaie, Leaqaa A., Raheem J. Muhasin та Mazin N. Mousa. "Synthesis, characterization and evaluation of antiinflammatory properties of novel α, β-unsaturated ketones". Tropical Journal of Pharmaceutical Research 19, № 1 (2020): 147–54. http://dx.doi.org/10.4314/tjpr.v19i1.22.

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Purpose: To prepare and characterize alicyclic aromatic chalcone derivatives, and study their antibiotic and anti-inflammatory properties.Methods: Claisen-Schmidt (aldol condensation) base-catalyzed condensation was used for preparation of chalcone derivatives (compounds I - IV), and the products were characterized using ultraviolet-visible spectroscopy (UV), FT-IR spectroscopy, proton nuclear magnetic resonance (1H-NMR), carbone 13CNMR and mass spectroscopy (MS). The antibacterial effect of the compounds was determined against Baci. cereus, Staph. Aureus, E. coli, and Pseudomonas Aeruginosa.
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6

FUELOEP, F., I. HUBER, and G. BERNATH. "ChemInform Abstract: Cyclic Aminoalcohols and Related Compounds. Part 39. Simple Synthesis of Alicyclic 1,3-Amino Alcohol Analogues of CNS-Active Compounds." ChemInform 28, no. 18 (2010): no. http://dx.doi.org/10.1002/chin.199718101.

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Hernáez, M. J., E. Andújar, J. L. Ríos, S. R. Kaschabek, W. Reineke, and E. Santero. "Identification of a Serine Hydrolase Which Cleaves the Alicyclic Ring of Tetralin." Journal of Bacteriology 182, no. 19 (2000): 5448–53. http://dx.doi.org/10.1128/jb.182.19.5448-5453.2000.

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ABSTRACT A gene designated thnD, which is required for biodegradation of the organic solvent tetralin by Sphingomonas macrogoltabidus strain TFA, has been identified. Sequence comparison analysis indicated that thnD codes for a carbon-carbon bond serine hydrolase showing highest similarity to hydrolases involved in biodegradation of biphenyl. An insertion mutant defective in ThnD accumulates the ring fission product which results from the extradiol cleavage of the aromatic ring of dihydroxytetralin. The gene product has been purified and characterized. ThnD is an octameric thermostable enzyme
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8

Shanker Pandey, Karuna, Murlidhar Jaywantrao Mendki, Karumuru Mallikarjuna Rao, and Ramamoorthy Vaidyanathaswamy. "Synthesis and Bioevaluation of Alicyclic and Heterocyclic Alkanoates as Cockroach Attractants." Bioscience, Biotechnology, and Biochemistry 59, no. 4 (1995): 725–27. http://dx.doi.org/10.1271/bbb.59.725.

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Gutierrez-Lara, Erika, Carlos Martínez-Conde, Edgar Rosales-Ortega, et al. "Synthesis and In Vitro AMPK Activation of Cycloalkyl/Alkarylbiguanides with Robust In Vivo Antihyperglycemic Action." Journal of Chemistry 2017 (2017): 1–8. http://dx.doi.org/10.1155/2017/1212609.

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This work describes the design, synthesis in one step, and the in vitro, in vivo, and in silico antidiabetic evaluation of a series of ten alicyclic and aromatic (alkyl +aryl: alkaryl)biguanides, analogues of metformin and phenformin. The design was conceived using isosteric replacement, chain-ring transformation, and lower and higher homologation strategies. All compounds were obtained as crystals and their structure was confirmed on the basis of their spectral data (NMR and mass spectra), and their purity was ascertained by microanalysis. Compounds were in vitro evaluated as activators of AM
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KARAMYSHEVA, L. A., S. I. TORGOVA, I. F. AGAFONOVA, R. KH GEIVANDOV, V. V. BYKOVA, and P. A. BURYLIN. "ChemInform Abstract: Liquid-Crystalline Alicyclic Compounds. Part 3. Synthesis and Isomorphism of Ethers and Esters Containing the Phenylcyclohexane Fragment." ChemInform 24, no. 10 (2010): no. http://dx.doi.org/10.1002/chin.199310171.

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Dissertations / Theses on the topic "Alicyclic compounds – Synthesis ; Microbiology"

1

Hiralal, Lettish. "Effect of fermentation and nutritional conditions on the profile of flavour active ester compounds in beer." Thesis, 2011. http://hdl.handle.net/10413/9061.

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During fermentation, the yeast Saccharomyces cerevisiae produces a broad range of aroma-active esters that are important for the desirable complex flavour of beer. The sensory threshold levels of these esters in beer are low, ranging from 0.2 ppm for isoamyl acetate to 15-20 ppm for ethyl acetate. Although esters are only present in trace amounts in beer, they are extremely important as minor changes in their concentration may have dramatic effects on beer flavour. Therefore, optimization of the concentrations of these aroma-active esters in beer is of interest in beer brewing. The number and
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Books on the topic "Alicyclic compounds – Synthesis ; Microbiology"

1

L, Novák, ed. Selective biocatalysis: A synthetic approach. VCH, 1992.

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