• 제목/요약/키워드: $\alpha$,$\beta$-Unsaturated aldehyde

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A New HPLC-analytical Method for Total Sphingosine Contents as an Indirect Index for the Ganglioside Contents of Deer Antlers

  • Choi, Hye-Ok;Kim, Jeung-Won;Jo, Sung-Jun;Kim, Jung-Hwan;Han, Byung-Hoon
    • Natural Product Sciences
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    • 제17권4호
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    • pp.315-320
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    • 2011
  • Routinely applicable HPLC assay procedures for the ganglioside content in various deer antler preparations were established through the creation of a UV-absorbing chromophoric substance - trans-${\alpha},{\beta}$-unsaturated-hexadecene-aldehyde - from the sphingosine moiety in ganglioside molecules by two step chemical reactions. In order to guarantee the assay's accuracy and sensitivity, the HPLC-assay procedure adopted internal reference procedures by mixing cis-${\alpha},{\beta}$-unsaturated-hexadecene aldehyde[V] or cis-3-heptadecene- 1,2-diol[IV] to assay samples. The internal reference compound [IV] or [V] was synthesized in our laboratory starting from mannitol-diacetonide through three or four step organic reactions. This new HPLC-assay procedure was successfully applied to deer antler extracts with good dose-dependent calibration curves at the picomole level of gangliosides.

${\alpha}$,${\beta}$-不飽和 카르보닐化合物의 還元 아미노화反應 (Reductive Amination of ${\alpha}$,${\beta}$-Unsaturated Carbonyl Compounds with Tetracarbonylhydridoferrate as a Reducing Agent)

  • 김홍석;심상철;심상철
    • 대한화학회지
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    • 제23권2호
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    • pp.99-103
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    • 1979
  • 세개의 ${\alpha}$,${\beta}$-불포화알데히드, 신남알데히드, 크로톤알데히드, 아크로레인을 여러가지 일차 아민 존재하에서 테트라카르보닐철산염으로 환원시켜 상당히 다른 수득률로 N-알킬아민을 합성하였다. 보통, $KHFe(CO)_4$ (22mmole)와 일차아민(22∼44mmole)과 ${\alpha}$,${\beta}$-불포화 알데히드 (22mmole)를 에탄올 용매에 넣고 일산화탄소 분위기하에 실온에서 9∼60시간 자석 젓개로 저어주면 일산화탄소를 천천히 흡수하면서 반응이 진행된다. 생성물은 가스크로마토그래피, 질량분석스펙트럼, 핵자기공명스펙트럼, 적외선스펙트럼 등으로 그 구조를 알았다.

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메타아크릴 알데히드의 선택적 수소화에서 2가 알코올의 이합체 형성 부반응 억제효과 (Inhibition of Side Reactions Forming Dimers of Diols in the Selective Hydrogenation of Methacryl Aldehyde)

  • 신국승;차미선;강경구;이창수
    • 청정기술
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    • 제29권2호
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    • pp.79-86
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    • 2023
  • Ru-MACHO-BH 촉매는 α, β-불포화 알데히드 화합물들의 카르보닐기(carbonyl group)만을 선택적으로 수소화 반응을 수행할 수 있다. 그러나 α, β-불포화 알데히드의 수소화 반응은 불균일 딜즈-앨더 반응을 수반하여 부산물인 이합체를 다량 생성한다. 본 연구에서는 Ru-MACHO-BH (Carbonyl hydrido (tetrahydroborato) [bis (2-diphenyl phosphino ethyl) amino] ruthenium(II)) 촉매를 이용하여, α, β-불포화 알데히드의 한 종류인 메타아크릴 알데히드(methacryl aldehyde) 화합물의 카르보닐기만 선택적으로 수소화 반응을 시켜 메타아릴 알코올(methallyl alcohol)을 합성하며, 동시에 2가 알코올을 부반응 억제제로 적용하였다. 이 결과는 모노 에틸렌 글리콜(mono ethylene glycol)이 이합체의 생성을 현저히 저감 시킬 수 있음을 보여주고 있다. 이러한 결과를 바탕으로 비닐기의 화학적 상호작용을 효과적으로 억제할 수 있는 하이드로퀴논을 사용하여 메타아크릴 알데히드에 존재하는 비닐기의 이합체 형성을 효과적으로 억제할 수 있었으며, 결국 메타아크릴 알데히드의 전환율을 상승시킬 수 있었다. 최종적으로, 고가의 귀금속 균일촉매인 Ru-MACHO-BH의 투입량을 1/10로 줄인 상태에서 원하는 생성물인 메타아릴 알코올의 선택도는 약 90% 이상, 수율은 약 80% 이상을 확보할 수 있었다. 이 결과는 수율 감소를 최소화하는 동시에 고가의 촉매 사용량을 저감하여 경제성을 향상시킬 수 있는 방법을 찾을 수 있게 하였다.

Selective Reduction by Lithium Bis-or Tris(dialkylamino)-aluminum Hydrides. II. Reaction of Lithium Tris(dibutylamino)-aluminum Hydride with Selected Organic Compounds Containing Representative Functional Groups

  • Cha, Jin-Soon;Lee, Sung-Eun;Lee, Heung-Soo
    • Bulletin of the Korean Chemical Society
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    • 제12권6호
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    • pp.644-649
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    • 1991
  • The approximate rates and stoichiometry of the reaction of excess lithium tris(dibutylamino)aluminum hydride (LT-DBA) with selected organic compounds containing representative functional groups under standardized conditions (tetrahydrofuran, $0^{\circ}C$) were studied in order to characterize the reducing characteristics of the reagent for selective reductions. The reducing ability of LTDBA was also compared with those of the parent lithium aluminum hydride and the alkoxy derivatives. The reagent appears to be much milder than the parent reagent, but stronger than lithium tri-t-butoxyaluminohydride in reducing strength. LTDBA shows a unique reducing characteristics. Thus, the reagent reduces aldehydes, ketones, esters, acid chlorides, epoxides, and amides readily. In addition to that, ${\alpha},{\beta}$-unsaturated aldehyde is reduced to ${\alpha},{\beta}$-unsaturated alcohol. Quinones are reduced to the corresponding diols without evolution of hydrogen. Tertiary amides and aromatic nitriles are converted to aldehydes with a limiting amount of LTDBA. Finally, disulfides and sulfoxides are readily reduced to thiols and sulfides, respectively, without hydrogen evolution.

Long Chain Dicationic Phase Transfer Catalysts in the Condensation Reactions of Aromatic Aldehydes in Water Under Ultrasonic Effect

  • Esen, Ilker;Yolacan, Cigdem;Aydogan, Feray
    • Bulletin of the Korean Chemical Society
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    • 제31권8호
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    • pp.2289-2292
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    • 2010
  • Long chain dicationic ammonium salts were used successfully as phase transfer catalyst in the condensation reactions of aromatic aldehydes in water under ultrasonic irradiation for the first time. The quaternary salt having longer distance between the cation centers was more effective than the mono- and dicationic ones having short chain.

Korean Red Ginseng water extract inhibits COX-2 expression by suppressing p38 in acrolein-treated human endothelial cells

  • Lee, Seung Eun;Park, Yong Seek
    • Journal of Ginseng Research
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    • 제38권1호
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    • pp.34-39
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    • 2014
  • Cigarette smoke is considered a major risk factor for vascular diseases. There are many toxic compounds in cigarette smoke, including acrolein and other ${\alpha},{\beta}$-unsaturated aldehydes, which are regarded as mediators of inflammation and vascular dysfunction. Furthermore, recent studies have revealed that acrolein, an ${\alpha},{\beta}$-unsaturated aldehyde in cigarette smoke, induces inflammatory mediator expression, which is known to be related to vascular diseases. In this study, we investigated whether Korean Red Ginseng (KRG) water extract suppressed acrolein-induced cyclooxygenase (COX)-2 expression in human umbilical vein endothelial cells (HUVECs). Acrolein-induced COX-2 expression was accompanied by increased levels of phosphorylated p38 in HUVECs and KRG inhibited COX-2 expression in HUVECs. These results suggest that KRG suppresses acrolein-induced COX-2 expression via inhibition of the p38 mitogen-activated protein kinase signaling pathway. In addition, KRG exhibited an inhibitory effect on acrolein-induced apoptosis, as demonstrated by annexin Vepropidium iodide staining and terminal deoxynucleotidyl transferase-mediated dUTP nick end-labeling assay. Consistent with these results, KRG may exert a vasculoprotective effect through inhibition of COX-2 expression in acrolein-stimulated human endothelial cells.

Selective Reduction of Organic Compounds with Non-Free Hydride Reducing Agents

  • Cha, Jin Soon
    • 통합자연과학논문집
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    • 제1권3호
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    • pp.192-194
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    • 2008
  • A series of non-free hydride reducing systems containing boron or aluminum atom, which possess no metal-hydride bond but an available hydrogen at a branched ${\beta}$-position, has been applied to the selective reduction (chemo--, regio-, and stereoselective reduction) of organic compounds. The systems, comprised of diisopinocampheylborane and diisobutylalane derivatives, exhibited almost perfect selectivities in the reduction of aldehydes and ketones. The characteristics features of this systems leading to a perfect transformation have been depicted in this report, especially in the 1) Reduction of ${\alpha}$,${\beta}$-Unsaturated Carbonyl Compounds to Allylic Alcohols via 1,2-Reduction, 2) Chemoselective Reduction between Structurally Different Carbonyl Compounds, and 3) Stereoselective Reduction of Cyclic Ketones.

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α, β-불포화 알데히드의 선택적 수소화 반응성 향상을 위한 전처리 방법 (Pretreatment for Improving Selective Hydrogenation Reaction of α, β-Unsaturated Aldehydes)

  • 신국승;차미선;이창수
    • Korean Chemical Engineering Research
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    • 제61권1호
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    • pp.168-174
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    • 2023
  • 일반적인 메틸 메타아크릴레이트(methyl methacrylate) 상업 공정의 중간체인 메타아크릴 알데히드(methacryl aldehyde)에는 불순물이 존재한다. 이는 전체 화학 반응의 전환율과 선택도가 크게 저하되는 원인이며 메타아릴 알코올(methallyl alcohol) 생산성 향상의 주요 문제이다. 본 연구는 다양한 불순물 중에서 반응성 저하의 주요 원인이 산(acid)임을 발견하였다. 불순물로 존재하는 산은 촉매의 활성을 급격하게 저하시키며, 부반응인 불균일 딜스-알더 반응(hetero Diels-Alder reaction)이 촉진됨을 확인하였다. 따라서, 메타아크릴 알데히드의 카르보닐기(carbonyl group)를 선택적으로 수소화하는 반응에서 반응 불순물인 산을 제거하기 위해 전처리 방법을 비교 평가하였고, 생산성을 향상시키기 위한 효과적인 방법을 제안하였다. 이를 통해 제안된 조건 하에서 최적의 선택적 수소화 반응 조건을 완성하였다.

Synthesis of Certain Mercapto and Aminopyrimidine Derivatives as Potential Antimicrobial Agents

  • El-Kerdawy, M.M.;Eisa, H.M.;El-Emam, A.A.;Massoud, M.A.;Nasr, M.N.
    • Archives of Pharmacal Research
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    • 제13권2호
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    • pp.142-146
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    • 1990
  • Reaction of ethyl 4-chloro-2-phenylpyrimidine-4-carboxylate (4) with 5-chloro-2-methylthiophenol or 3-aryl-4-phenyl-1, 2, 4-triazole-5 thiol yielded the corresponding thioethers (5) and (8a, b), respectively. Careful alkaline hydrolysis of (5) yielded the corresponding carboxylic acid (6). Reaction of (4) with p-aminoacetophenone yielded compound (10) which was reacted with certain aromatic aldehyde to afford the$\alpha,\beta$-unsaturated ketones (11a-d). Condensation of (11a-d) with malononitrile or phenylhydrazine yielded the 2-amino-3-cyanopyridines (12a-f) or the 2-pyrazolines (13a, b) respectively. Seven representative compounds were tested for their in vitro antimicrobial activity against some pathogenic micro-organisms, some of them were proved to be active.

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