• Title/Summary/Keyword: furan

Search Result 264, Processing Time 0.028 seconds

CONFORMATIONAL ANALYSIS ON THE C$_4$-PHOTOCYCLODIMERS OF 4,$5^1$,8-TRIMETHYLPSORALEN

  • Kim, Ja-Hong
    • Journal of Photoscience
    • /
    • v.2 no.2
    • /
    • pp.99-101
    • /
    • 1995
  • A semiempirical methods(PM3-CI-UHF, MM2) for the evaluation of ground and excited state electronic structures of electron-donating substituents are applied to 4, 5', 8-trimethylpsoralen(TMP) with TMP dimer. Three types of product have been proposed; (1) pyrone< >pyrone, (2) pyrone< >furan, (3) hetero dimer resulting from the C$_4$-cycloaddition between the furan end of one TMP moiety and the pyrone end of the other, with cis-syn configuration.

  • PDF

Cirsiumaldehyde from Gastrodia elata

  • YunChoi, Hye-Sook;Pyo, Mi-Kyung;Park, Kyung-Mi
    • Natural Product Sciences
    • /
    • v.3 no.2
    • /
    • pp.104-105
    • /
    • 1997
  • In the course of continous work on tubers of Gastrodia elata, a new constituent was isolated from the ethyl acetate soluble fraction prepared from the methanol extract. The structure of the compound was identified as ${\alpha},{\alpha}'-[bis-2-(5-carboxaldehydo)furanyl]-dimethyl$ ether from the elemental analytical and spectroscopic data. This compound was once isolated from Cirsium chlorolepis and named as cirsiumaldehyde. This is the first furan type compound isolated from Gastrodia elata.

  • PDF

Convenient Route to Core-modified Corroles by Acid-catalyzed Condensation of Furylpyrromethanes and Dipyrromethanes

  • Lee, Chang Hui;Jo, Won Seop;Ga, Jae Won;Kim, Han Jae;Lee, Pil Ho
    • Bulletin of the Korean Chemical Society
    • /
    • v.21 no.4
    • /
    • pp.429-433
    • /
    • 2000
  • Corroles and oxacorroles were synthesized by acid-catalyzed, 2+2 condensation. The condensation afforded different corroles bearing core-heteroatoms at the predesignated locations. Regioselective a- a’ linkage be-tween pyrrole and furan or betwee n pyrrole and pyrrole was achieved by keeping the linking carbon at different position of starting dipyrromethanes. The condensation was only fruitful when furan-containing dipyrromethanes were condensed.

Analysis of Volatile Components of a Chicken Model Food System in Retortable Pouches (레토르트 파우치 계육 모형식품의 휘발성분 분석)

  • Choi, Jun-Bong;Chung, Ha-Yull;Kong, Un-Young;Moon, Tae-Wha
    • Korean Journal of Food Science and Technology
    • /
    • v.28 no.4
    • /
    • pp.772-778
    • /
    • 1996
  • In order to investigate changes of flavor during food sterilization in retortable pluches, a model food system consisting of 50% chicken breast meat, 1% salt and 49% chicken stock was analyzed before and after retorting using GC and GC-MS. In the analysis of the volatile components collected by the nitrogen purge and trap technique before and after retorting, a total of 53 peaks were observed on chromatograms and 42 peaks were identified. Among the 42 peaks identified were 17 caused by aldehydes, 9 by hydrocarbons, 8 by alcohols, 6 by ketones, 1 by furan and 1 by terpene. Analysis of the data obtained from our model food system strongly suggested that the compounds responsible for retort flavor are 2-heptanone, 2-pentyl furan and various ketones.

  • PDF

Synthesis of Strigol Analogues (Strigol 유사체의 합성)

  • Kim In Kyu;Hong Young Tech;Kim Sung Soo
    • Journal of the Korean Chemical Society
    • /
    • v.36 no.5
    • /
    • pp.764-769
    • /
    • 1992
  • Strigol, a natural product isolated from root exudates of cotton, was found to be an extremely potent seed germination stimulant for the parasitic plant, witchweed. Witchweed seeds can remain dormant in the soil for several years until favorable conditions prevail including exposure to some type of chemical germination stimulant. Several strigol analogues, 3-methyl-4-(2-oxo-3,3a,6,6a-tetrahydro-2H-cyclopenta[b]furan-3-ylidenemethoxy)-but-2-en-4-olide(21), 4-(2-oxo-3,3a,6,6a-tetrahydro-2H-cyclopenta[b]furan-3-ylidenemethoxy)but-2-en-4-oilde(22), 3-methyl-4-(2-oxotetrahydrofuran-3-ylidenemethoxy)-but-2-en-4-olide(23), and 4-(2-oxotetrahydrofuran-3-ylidenemethoxy)-but-2-en-4-olide(24), were synthesized.

  • PDF

1-Furan-2-yl-3-Pyridine-2-yl-Propenone Inhibits TNF-${\apha}$-induced Intestinal Inflammation via Suppression of MCP-1 and IL-8 Expressions in HT-29 Human Colon Epithelial Cells (1-Furan-2-yl-3-pyridin-2-yl-propenone의 TNF-${\apha}$ 유도성 MCP-1과 IL-8의 발현 억제를 통한 장 상피세포 염증 억제효과)

  • Kim, Kyoung-Jin;Kim, Jong-Tae;Lee, Eung-Seok;Lee, Jong-Suk;Kim, Jung-Ae
    • YAKHAK HOEJI
    • /
    • v.52 no.5
    • /
    • pp.402-406
    • /
    • 2008
  • Previously, we have shown that 1-furan-2-yl-3-pyridin-2-yl-propenone (FPP-3) has an anti-inflammatory activity in a rat paw-edema model. In the present study, we investigated an inhibitory effect of FPP-3 on the tumor necrosis factor (TNF)-${\apha}$-induced inflammatory cytokine response in HT-29 human colon epithelial cells. Treatment with FPP-3 significantly prevented the TNF-${\apha}$-induced attachment of leukocytes to HT-29 colon epithelial cells, which is one of the pathologic hallmarks in colon inflammation. The effect of FPP-3 was markedly superior than that of 5-aminosalicylic acid (5-ASA), a commonly used drug for the treatment of inflammatory bowel disease (IBD). The pretreatment with FPP-3 inhibited TNF-${\apha}$- induced monocyte chemoattractant protein (MCP)-1, interleukin (IL)-8 mRNA expressions. In addition, FPP-3 significantly suppressed TNF-${\apha}$-induced nuclear factor (NF)-${\kappa}B$ transcription activity. These results demonstrate that FPP-3 modulates intestinal inflammation via suppressing the NF-${\kappa}B$ dependent expressions of MCP-1 and IL-8, and suggest that FPP-3 may be a valuable agent for the treatment of IBD.

Polymerization and Characterization of Polyesters Using Furan Monomers from Biomass (Biomass 유래 퓨란계 단량체를 이용한 폴리에스터의 중합 및 특성 연구)

  • Seo, Kang-Jin;Kim, Myeong-Jun;Jeong, Ji-Hea;Lee, Young-Chul;Noh, Si-Tae;Chung, Yong-Seog
    • Polymer(Korea)
    • /
    • v.35 no.6
    • /
    • pp.526-530
    • /
    • 2011
  • Furan-2,5-dicarboxylic acid (FDCA) was synthesized by $KMnO_4$ oxidation of 2,5-dihydroxymethylfuran(DHMF) derived from biomass. Polyesters were synthesized by esterification and polycondensation of FDCA with various diols(ethane-1,2-diol, propane-1,3-diol, butane-1,4-diol, hexane-1,6-diol, decane-1,10-diol). The composition of polyesters was characterized by using $^1H$ NMR. Thermal properties of the polyesters were characterized by DSC and TGA. Intrinsic viscosities(IV) of the polyesters were measured to be 0.78~1.2 dL/g comparable with IV of commercial poly(ethylene terephthalate)(PET). As the chain lengths of diols increased, Young's modulus and strength decreased and elongation-to-break generally increased. Young's modulus and strength of the polyesters were measured to be 3551 MPa and 103 MPa, respectively, comparable with commercial PET.

Synthesis of Ligands Containing Thiophene- or Furan- groups and Determination of Stability Constants of Chelating Compounds for Removal of Heavy Metals (Cd 2+,Pd 2+,Zn 2+,Cu 2+) in Aqueous Solution (수용액 중의 중금속 (Cd 2+,Pd 2+,Zn 2+,Cu 2+)이온 분리를 위한 티오펜 및 퓨란기를 포함하는 리간드들의 합성과 착화합물의 안정도상수 결정)

  • Kim, Jun Gwang;Kim, Jeong Seong
    • Journal of Environmental Science International
    • /
    • v.13 no.4
    • /
    • pp.435-440
    • /
    • 2004
  • The thiophene or furan-containing hexadentate ligands 1, 12-bis (2-theophene )-2,5,8,ll-tetraazadodecane(Thiotrien ㆍ 4HCl) and 1,12-bis (2-furan)-2,5,8,11-tetraazadodecane(Furatrienㆍ4HC1) were synthesized as their tetrahydrochloride salt and characterized by EA, IR, NMR, and Mass spectrum. Their protonation constants (logK$_{nH}$) and stability constants (logK$^{M}_{L}$ for Cd$^{2+}$, Pb$^{2+}$, $Zn^{2+}$ and Cu$^{2+}$ ions were determined in aqueous solution by potentiometry and compared with 1, 12-bis(2-pyridyl)-2,5,8, 11-tetra-azadodecane(Pytrien) of pyridyl-containing ligand. The effect stability constants of ligands and metal ion for removal of heavy metals in aqueous solution were described.