• Title/Summary/Keyword: Tetracyclic

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Synthesis of Imidazo[1,2-a]pyridines and Pyrido[1,2-a]pyrimidines in Water and their SNAr Cyclizations

  • Chanu, Langpoklakpam Gellina;Singh, Thokchom Prasanta;Jang, Yong Ju;Yoon, Yong-Jin;Singh, Okram Mukherjee;Lee, Sang-Gyeong
    • Bulletin of the Korean Chemical Society
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    • v.35 no.4
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    • pp.994-1000
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    • 2014
  • Synthesis of tetrahydroimidazo[1,2-a]pyridines and tetrahydropyrido[1,2-a] pyrimidines by a one-pot and three component reaction of ${\alpha}$-oxoketenedithioacetals, diamines and DMAD in water has been described. Different routes for accessing the desired compounds were examined and a few specially designed-substrates have been utilized further to afford the new imidazo and pyrido fused [1,8] naphthyridine tetracyclic compound by $S_NAr$ intramolecular cyclization.

A Model Study toward the Synthesis of Xestoquinone and Halenaquinone

  • Ahn, Chan-Mug;Woo, Ho-Bum
    • Proceedings of the PSK Conference
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    • 2003.04a
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    • pp.240.2-240.2
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    • 2003
  • A strategy for synthesis of the furan-fused tetracyclic core of xestoquinone and halenaquinone was explored through a model study. Methyl 8-oxo-4-methyl-4-phenyl-2,7-nonadiynoate was prepared from hydratroponitrile and 3-butyn-1-ol as starting materials. The intramolecular cycloaddition of this intermediate as a key step will be involved.

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Facile Formation of Unexpected [m,6,n]-tricyclic Spiranes via Intramolecular [3+2] Cyclization of Platinum-bound Pyrylium with Alkenes

  • Oh, Chang-Ho;Tak, Sang-Yong;Lee, Ji-Ho;Piao, Lanhua
    • Bulletin of the Korean Chemical Society
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    • v.32 no.spc8
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    • pp.2978-2980
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    • 2011
  • Enynals bearing an olefinic pendant were successfully cyclized via Huisgen-type [3+2] cycloaddition to the tetracyclic Pt-carbene complexes which would undergo insertion into a C-H bond of the ${\beta}$-position to afford the fused cyclopropane intermediates. Their tandem rearrangement afforded diverse types of spiranes depending on the tethered alkenes of the enynals.

The Use of Psychotropics in Patients with Renal Diseases (신장질환환자들에서 향정신성 약물의 사용)

  • Koh, Kyung-Bong
    • Korean Journal of Psychosomatic Medicine
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    • v.1 no.1
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    • pp.25-34
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    • 1993
  • The author reviewed the general principle in the use of psychotropics for patients with renal diseases. who have psychiatric problems. Durgs which are dialyzable and metabolized or eliminated by kidney should not be used for patients with renal failure. However, lithium can be effectively used in a single dose$(300{\sim}600 mg/day)$ after each dialysis. though lithium has the double negative components. It is recommended that serum lithium level should be frequently monitored and the dose of lithium should be gradually increased to minimize its side effect Most of other psychotropics such as benzodiazepine anxiolytics tricyclic or tetracyclic antidepressants, and neuroleptics are metabolized in the liver, and they can be used in renal patients. The dose of these drugs should be reduced in two-thirds of the standard dose. In addition. it is necessary for liaison psychiatrists and other physicians to understand the interactions between psychotropics and drugs often used for treatment of renal diseases in order to prescribe psychotropics safely and effectively in renal patients.

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New Geldanamycin Analogs from Streptomyces hygroscopicus

  • Wu, Cheng-Zhu;Jang, Jae-Hyuk;Ahn, Jong Seog;Hong, Young-Soo
    • Journal of Microbiology and Biotechnology
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    • v.22 no.11
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    • pp.1478-1481
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    • 2012
  • Geldanamycin (GM) and its analogs are important anticancer agents that inhibit heat shock protein (Hsp) 90, which is a major chaperone protein in cancer cells. Accordingly, based on interest in obtaining novel natural GM derivatives, the potential of Streptomyces hygroscopicus JCM4427, a GM producer, was explored for novel natural GM derivative(s), resulting in the discovery of new GM analogs as a biosynthetic shunt product and intermediates from its fermentation broth. In this study, the fermentation, isolation, structure determination, and biological activity of the compounds, two new tetracyclic thiazinogeldanamycin (1) and 19-hydroxy-4,5-dihydrogeldanamycin (3), together with the three known 4,5-dihydrothiazinogeldanamycin (2), reblastatin (4), and 17-demethoxy-reblastatin (5), are described.

Anticancer and Antiviral Effect of Some Triterpenes Isolated from the Natural Sources

  • Kim, Young-Sup;Choi, Sang-Un;Lee, Chong-Ock;Lee, Chong-Kyo;Ryu, Shi-Yong
    • Proceedings of the PSK Conference
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    • 2002.10a
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    • pp.138-139
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    • 2002
  • The diverse, widespread, and exceedingly numerous family of natural products constructed from five carbon building-units and so comprising compounds with $C_{5}$, $C_{10}$, $C_{15}$, $C_{20}$, ${\cdots}$, $C_{40}$ skeletons (together with a few higher members) are synoymously termed terpenes or terpenoids. Among the terpene classes, the triterpenes ($C_{30}$ skeletones) form the largest group and are widely distributed in the plant kingdom, either in the free state or as esters or glycosides, although a few important members found in the animal kingdom such as squalene and a number of tetracyclic component including lanosterol. (omitted)

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Structure of Cholesteryl Hemisuccinate (Cholesteryl Hemisuccinate의 구조)

  • Park, Young-Ja
    • Korean Journal of Crystallography
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    • v.15 no.1
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    • pp.29-34
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    • 2004
  • The crystal structure of cholesteryl hemisuccinate ($C_{31}H_{50}O_4$) was investigated by X-ray diffraction method. The cholesterol fragment of the title compound were in good agreement with those for related cholesterol derivatives. The unit cell contains four cholesteryl hemisuccinate molecules that are not related by crystal symmetry and have their tetracyclic system almost parellel to each other. There are two pairs of hydrogen-bonded dimer between A and D molecules and B and C molecules. These two hydrogen-bonded dimers are parallel to the c-axis, and are closely packed.

Triterpenoid Components of Betula latifolia $K_{OMAROV}$ -Isolation and Characterization of Triterpenoids- (자작나무 엽(葉)의 Triterpenoid 성분연구(成分硏究) -Triterpenoid의 분리(分離) 및 동정(同定)-)

  • Han, Byung-Hoon;Chi, Hyung-Joon;Han, Young-Nam
    • Korean Journal of Pharmacognosy
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    • v.4 no.4
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    • pp.167-172
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    • 1973
  • Five crystalline substances, which are positive to$L_{IEBERMAN}-B_{URCHARD}$ reaction, were isolated from the unsaponifiable fraction of the fresh leaves of Betula latifolia $K_{OMAROV}$ (Betulaceae)by silica gel column chromatographic purification. Compound $A\;(C_{29}H_{50}O,\;mp\;136^{\circ}), \;B\;(C_{30}H_{52}O_3,\;mp\;165^{\circ}), \;C\;(C_{30}H_{52}O_4,\;mp\;237^{\circ}), \;D\;(C_{30}H_{52}O_3,\;mp\;196^{\circ})\;and\; E\;(C_{30}H_{52}O_4,\;mp\;121^{\circ})$ were isolated. Compound B was characterized as a new tetracyclic triterpenoid. Compounds A, C and D were identified as ${\beta}-sitosterol$, betulatriterpene C, and betulafolienetriol, respectively.

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Mass Spectrometry of Dammarane Triterpenoids (Dammarane계(係) Triterpenoid의 질량분광분석(質量分光分析))

  • Han, Byung-Hoon;Kim, Jae-Hoon;Chi, Hyung-Joon
    • Korean Journal of Pharmacognosy
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    • v.10 no.2
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    • pp.55-59
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    • 1979
  • Mass spectra of the dammarane triterpenes having open side chain and $C_{20}-C_{25}-epoxy$ side chain were measured. Principal fragment ions were assigned and plausible mechanisms for the formation of the fragment ions were proposed. In general, the triter-penoids of $C_{20}-C_{25}-epoxy$ side chain. produce $h_{1}-species$ fragment ions by the deletion of side chain at $C_{20}-C_{22}$ bond and open side chain triterpenoids produce $h_{2}$ species fragmentions whose mass numbers are higher by two mass unit than those of $h_{1}$ species. The mass number of h species fragment ions will serve as the diagnostic tool for the elucidation of side chain structure of tetracyclic triterpenoids.

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