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Статті в журналах з теми "3-oxathiane"

Щоб переглянути інші типи публікацій з цієї теми, перейдіть за посиланням: 3-oxathiane.

Автор: Grafiati

Опубліковано: 10 грудня 2022

Оновлено: 29 січня 2023

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1

Varshnaya, Rohit Kumar, and Prabal Banerjee. "Construction of thiazines and oxathianes via [3 + 3] annulation of N-tosylaziridinedicarboxylates and oxiranes with 1,4-dithiane-2,5-diol: application towards the synthesis of bioactive molecules." Organic & Biomolecular Chemistry 15, no. 24 (2017): 5182–90. http://dx.doi.org/10.1039/c7ob00941k.

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Анотація:

Efficient construction of functionalized thiazine and oxathiane derivatives via [3 + 3] annulation of N-tosylaziridinedicarboxylates and oxiranes with in situ generated mercaptoaldehyde in the presence of a Lewis acid is described.

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2

Sun, Jingbo, Jinchang Wu, and Hua Yang. "Synthesis, Structure, and Conformation of 2′,3′-Fused Oxathiane and Thiomorpholine Uridines." Helvetica Chimica Acta 90, no. 10 (October 2007): 1917–24. http://dx.doi.org/10.1002/hlca.200790199.

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3

Arkhipov, A. Yu, and A. V. Anisimov. "2,4-dichloromethyl-1,5-diphenoxy-3-thiapentane in the synthesis of oxathiane crown ethers." Chemistry of Heterocyclic Compounds 31, no. 11 (November 1995): 1373–74. http://dx.doi.org/10.1007/bf01168636.

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4

KO, K. Y., and K. I. KIM. "ChemInform Abstract: Highly Diastereoselective Reduction of 2-Acyl-1,3-oxathiane 3-Oxides Derived from (1R)-(+)-Camphor." ChemInform 30, no. 3 (June 17, 2010): no. http://dx.doi.org/10.1002/chin.199903053.

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5

Hossaini, Zinatossadat, Faramarz Rostami-Charati, Samereh Seyfi, and Mehdi Ghambarian. "Multicomponent reactions for the synthesis of functionalized 1,4-oxathiane-3-thiones under microwave irradiation in water." Chinese Chemical Letters 24, no. 5 (May 2013): 376–78. http://dx.doi.org/10.1016/j.cclet.2013.03.003.

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6

Hahn, Hoh-Gyu, and Kee-Hyuk Chang. "Formation of Bicyclic b-Lactams from Dichloro-1,4-oxathiane-3-carboxanilides: Nucleophilic Substitution of Nitrogen on Anomeric Carbon." HETEROCYCLES 50, no. 2 (1999): 713. http://dx.doi.org/10.3987/com-98-s(h)61.

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7

Hossaini, Zinatossadat, Faramarz Rostami-Charati, Samereh Seyfi, and Mehdi Ghambarian. "ChemInform Abstract: Multicomponent Reactions for the Synthesis of Functionalized 1,4-Oxathiane-3-thiones under Microwave Irradiation in Water." ChemInform 44, no. 44 (October 14, 2013): no. http://dx.doi.org/10.1002/chin.201344156.

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8

Ko, Kwang-Youn, and Ho-Seop Yun. "Diastereoselective Reduction of Chiral 2-(1-Alkenoyl)- and 2-(1-Alkynoyl)-1,3-Oxathiane 3-Oxides Derived from (1R)-(+)-Camphor." Bulletin of the Korean Chemical Society 33, no. 7 (July 20, 2012): 2415–18. http://dx.doi.org/10.5012/bkcs.2012.33.7.2415.

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9

Hahn, Hoh-Gyu, та Kee-Hyuk Chang. "ChemInform Abstract: Formation of Bicyclic β-Lactams from Dichloro-1,4-oxathiane-3-carboxanilides: Nucleophilic Substitution of Nitrogen on Anomeric Carbon." ChemInform 30, № 29 (14 червня 2010): no. http://dx.doi.org/10.1002/chin.199929151.

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10

J.I., Nirmal Kumar, Megha Barot, and Shamiyan R. Khan. "Some Intermediate Bio-Transformants During Biodegradation of High Molecular Weight Phenanthrene and Fluoranthene by Cyanobacterial species – Aulosira Fertilissima Ghose." International Journal of Applied Sciences and Biotechnology 1, no. 3 (September 25, 2013): 97–105. http://dx.doi.org/10.3126/ijasbt.v1i3.8232.

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The PAHs compounds are known to be carcinogenic, teratogenic, mutagenic and toxic to all living organism. Handful of literature is available on biodegradation of these compounds by bacteria and fungi, however, scanty work is done by using microalgae on biodegradation of these two PAHs. In this investigation, the efficiency of Aulosira fertilissima Ghose to remove fluoranthene (0.001gm.ml-1), phenanthrene (0.001gm.ml-1) and a mixture of both (each at concentration of 0.0005gm.ml-1) were evaluated for intermediate bio-transformants during biodegradation by using GCMS. The result showed that the efficiency of Aulosira fertilissima for removal and biodegradation of phenanthrene was higher than fluoranthene, indicate fluoranthene was more stable and recalcitrant. PAHs uptake after 7-days of treatment was 80% and 66% of these phenanthrene and fluoranthene, respectively by the cyanobacteria. The synergetic effect of fluoranthene on phenanthrene was observed, presence of fluoranthene stimulate the degradation of phenanthrene due to which phenanthrene produce more bio-transformants. Some intermediates were observed like Methyl linoleate, 4-(2,2- dimethyl-6-methylenecyclohexylidene)-3-methyl-,(Z)- etc. for phenanthrene biodegradation process while 2,3-dihydrofluoranthene, (1R,5R)-2-isopropyl-5-methylcyclohexanol, for fluoranthene degradation. Moreover, 3-isopropylidene-2,2-dimethyl-6-phenyl-1,4-oxathiane, 7- phenyltridecane, diphenylacetylene, for mixture of two PAHs applied.DOI: http://dx.doi.org/10.3126/ijasbt.v1i3.8232 Int J Appl Sci Biotechnol, Vol. 1(3) 2013 : 97-105

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11

Halperin Kuhns, Victoria L., Jason Sanchez, Dylan C. Sarver, Zoya Khalil, Premraj Rajkumar, Kieren A. Marr, and Jennifer L. Pluznick. "Characterizing novel olfactory receptors expressed in the murine renal cortex." American Journal of Physiology-Renal Physiology 317, no. 1 (July 1, 2019): F172—F186. http://dx.doi.org/10.1152/ajprenal.00624.2018.

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The kidney uses specialized G protein-coupled receptors, including olfactory receptors (ORs), to act as sensors of molecules and metabolites. In the present study, we cloned and studied seven renal ORs, which we previously found to be expressed in the murine renal cortex. As most ORs are orphan receptors, our goal was to identify ligands for these ORs in the hope that this will guide future research into their functional roles. We identified novel ligands for two ORs: Olfr558 and Olfr90. For Olfr558, we confirmed activation by previously reported ligands and identified 16 additional carboxylic acids that activated this OR. The strongest activation of Olfr558 was produced by butyric, cyclobutanecarboxylic, isovaleric, 2-methylvaleric, 3-methylvaleric, 4-methylvaleric, and valeric acids. The primary in vivo source of both butyric and isovaleric acids is gut microbial metabolism. We also identified 14 novel ligands that activated Olfr90, the strongest of which were 2-methyl-4-propyl-1,3-oxathiane, 1-octen-3-ol, 2-octanol, and 3-octanol. Interestingly, 8 of these 14 ligands are of fungal origin. We also investigated the tissue distribution of these receptors and found that they are each found in a subset of “nonsensory” tissues. Finally, we examined the putative human orthologs of Olfr558 and Olfr90 and found that the human ortholog of Olfr558 (OR51E1) has a similar ligand profile, indicating that the role of this OR is likely evolutionarily conserved. In summary, we examined seven novel renal ORs and identified new ligands for Olfr558 and Olfr90, which imply that both of these receptors serve to detect metabolites produced by microorganisms.

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12

Pihlaja, Kalevi, Reijo Sillanp��, Martti Dahlqvist, G�za St�jer, and Markku Ahlgren. "Conformational analysis 29: Preparation and1H and13C NMR, FTIR, MS, and crystallographic conformational and configurational study of 3-Oxo-1,3-oxathiane and its monomethyl derivatives." Structural Chemistry 4, no. 3 (June 1993): 203–10. http://dx.doi.org/10.1007/bf00679347.

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13

PIHLAJA, K., R. SILLANPAEAE, M. DAHLQVIST, G. STAJER, and M. AHLGREN. "ChemInform Abstract: Conformational Analysis. Part 29. Preparation and 1H and 13C NMR, FTIR, MS, and Crystallographic Conformational and Configurational Study of 3-Oxo-1,3-oxathiane and Its Monomethyl Derivatives." ChemInform 24, no. 43 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199343054.

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14

Samzadeh-Kermani, Alireza. "Silver salt catalyzed synthesis of 1,4-oxathian-3-imine derivatives." Tetrahedron 72, no. 35 (September 2016): 5301–4. http://dx.doi.org/10.1016/j.tet.2016.06.072.

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15

Sizov, A. Yu, A. F. Kolomiets, and A. V. Fokin. "Formation of 2,2-difluoro-3-hydroxymethylbenzo-1,4-oxathianes from 2-(?-trifluoromethylvinylthio)phenols)." Russian Chemical Bulletin 43, no. 8 (August 1994): 1381–83. http://dx.doi.org/10.1007/bf00703699.

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16

WALKUP, R. D., та P. D. JUN BOATMAN. "ChemInform Abstract: Preparation of 4-Alkanesulfinyl-δ4-1,3-oxathianes and δ4-1, 3-Oxathianes. On the Resistance of Endocyclic Ketene Dithioacetals to Nucleophilic Attack." ChemInform 24, № 36 (20 серпня 2010): no. http://dx.doi.org/10.1002/chin.199336196.

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17

Tschierske, Carsten, Detlev Joachimi, and Horst Zaschke. "Kristallin-flüssige Heterocycloalkane; Synthese kristallin-flüssiger 5-Alkyl-1, 3-oxathian-2-carbonsäureester." Zeitschrift für Chemie 28, no. 8 (August 31, 2010): 303–4. http://dx.doi.org/10.1002/zfch.19880280823.

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18

Juaristi, Eusebio, Gabriel Cuevas, and Abelardo Flores-Vela. "Stereoelectronic interpretation of the unusual perlin effects and 1H NMR chemical shifts in 1,3-oxathiane." Tetrahedron Letters 33, no. 46 (November 1992): 6927–30. http://dx.doi.org/10.1016/s0040-4039(00)60897-3.

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19

O’Sullivan, Orlagh C. M., Stuart G. Collins, Anita R. Maguire, Matthias Böhm, and Wolfram Sander. "Photochemistry ofcis-3-Diazo-5,6-dimethyl-1,4-oxathian-2-oneS-Oxide in Argon Matrices." European Journal of Organic Chemistry 2006, no. 13 (July 2006): 2918–24. http://dx.doi.org/10.1002/ejoc.200500971.

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20

Juaristi, E., A. Flores-Vela, V. Labastida, and M. Ordoñez. "Lack of manifestation of an anomeric effect in 2-diphenylphosphinoyl-1, 3-dioxane and 2-diphenylphosphinoyl-1, 3-oxathiane1." Journal of Physical Organic Chemistry 2, no. 4 (June 1989): 349–58. http://dx.doi.org/10.1002/poc.610020406.

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21

SIZOV, A. YU, A. F. KOLOMIETS, and A. V. FOKIN. "ChemInform Abstract: Formation of 2,2-Difluoro-3-hydroxymethylbenzo-1,4-oxathianes from 2-(. alpha.-Trifluoromethylvinylthio)phenols." ChemInform 26, no. 12 (August 18, 2010): no. http://dx.doi.org/10.1002/chin.199512205.

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22

Singer, Gabriele, Georg Heusinger, Armin Mosandl, and Christian Burschka. "Stereoisomere Aromastoffe, XVI. Struktur und Eigenschaften optisch reiner 2-Methyl-4-propyl-1,3-oxathian-3-oxide." Liebigs Annalen der Chemie 1987, no. 5 (May 15, 1987): 451–53. http://dx.doi.org/10.1002/jlac.198719870352.

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23

Hahn, Hoh-Gyu, Joong-Kwon Choi, and Kee Dal Nam. "ChemInform Abstract: Anchimeric Assistance in the Rearrangement of Dichloro-3-methyl-1,4-oxathianes to 2-Chloromethyl Dihydro-1,4-oxathiins." ChemInform 30, no. 10 (June 17, 2010): no. http://dx.doi.org/10.1002/chin.199910048.

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24

Kenis, Sara, Matthias D'hooghe, Guido Verniest, Maaike Reybroeck, Tuyet Anh Dang Thi, Chinh Pham The, Tham Thi Pham, Karl W. Törnroos, Nguyen Van Tuyen, and Norbert De Kimpe. "Nucleophile-Directed Selective Transformation ofcis-1-Tosyl-2-tosyloxymethyl-3-(trifluoromethyl)aziridine into Aziridines, Azetidines, and Benzo-Fused Dithianes, Oxathianes, Dioxanes, and (Thio)morpholines." Chemistry - A European Journal 19, no. 19 (March 19, 2013): 5966–71. http://dx.doi.org/10.1002/chem.201204485.

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25

D'hooghe, Matthias, and et al et al. "ChemInform Abstract: Nucleophile-Directed Selective Transformation of cis-1-Tosyl-2-tosyloxymethyl-3-(trifluoromethyl)aziridine into Aziridines, Azetidines, and Benzo-Fused Dithianes, Oxathianes, Dioxanes, and (Thio)morpholines." ChemInform 44, no. 36 (August 15, 2013): no. http://dx.doi.org/10.1002/chin.201336089.

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26

CLAUS, P. K., and E. JAEGER. "ChemInform Abstract: CONFORMATIONAL EQUILIBRIA OF 1,3-OXATHIANE-3-IMIDES." Chemischer Informationsdienst 16, no. 5 (February 5, 1985). http://dx.doi.org/10.1002/chin.198505249.

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27

SINGER, G., G. HEUSINGER, A. MOSANDL, and C. BURSCHKA. "ChemInform Abstract: Stereoisomeric Flavor Compounds. Part 16. Structure and Properties of Optically Pure 2-Methyl-4-propyl-1,3-oxathiane 3-Oxides." ChemInform 18, no. 34 (August 25, 1987). http://dx.doi.org/10.1002/chin.198734215.

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28

Samzadeh-Kermani, Alireza. "ChemInform Abstract: Silver Salt Catalyzed Synthesis of 1,4-Oxathian-3-imine Derivatives." ChemInform 47, no. 50 (November 2016). http://dx.doi.org/10.1002/chin.201650138.

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29

SUOKAS, E., S. KALTIA, and J. KANSIKAS. "ChemInform Abstract: ACID CATALYZED REARRANGEMENT OF CARBOXIN AND THE X-RAY CRYSTAL STRUCTURE OF (E)-3-(1-ANILINOETHYLIDENE)-1,4-OXATHIAN-2-ONE." Chemischer Informationsdienst 16, no. 20 (May 21, 1985). http://dx.doi.org/10.1002/chin.198520226.

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