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Relevant bibliographies by topics / Octahydro-1

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Academic literature on the topic 'Octahydro-1'

Author: Grafiati

Published: 4 June 2021

Last updated: 2 February 2022

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Journal articles on the topic "Octahydro-1"

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Goodridge, RJ, TW Hambley, and DD Ridley. "Preparations and Crystal-Structures of the 2-Oxides of Some Octahydro-3,2,1-Benzoxathiazines and Octahydro-2h-3,1,2-Benzoxazaphosphorines." Australian Journal of Chemistry 39, no. 4 (1986): 591. http://dx.doi.org/10.1071/ch9860591.

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The cis -and trans-fused 1-benzyl-1,4,4a,5,6,7,8,8a-octahydro-3,2,1- benzoxathiazine 2- oxides and cis - and trans-fused 1-benzyl-2-phenyl-1,4,4a,5,6,7,8,8a-octahydro-2H-3,1,2-benzoxazaphosphorine 2-oxides have been prepared from the cis- and trans-2-benzylaminocyclohexanemethanols and their structures have been determined by n.m.r .and crystallographic methods.

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Peng, Wan Xi, Hong Chen Qi, Zhong Feng Zhang, and Lan Sheng Wang. "Py-GC/MS Analysis on Biomedicine of Benzene/Ethanol Extractives from Eucalyptus camaldulensis Biomass." Key Engineering Materials 467-469 (February 2011): 1702–5. http://dx.doi.org/10.4028/www.scientific.net/kem.467-469.1702.

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The benzene/ethanol extractives of Eucalyptus camaldulensis biomass were identified by Py-GC/MS to find out biomedical application. The main 350°С pyrolysis components were 1-phenanthrenecarboxylic acid, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)- (21.22%), .beta.-sitosterol acetate (6.4%), stigmasterol, 22,23-dihydro-(5.87%), ergosta-4,6,22-trien-3.beta.-ol(3.6%), etc. The main 350°С pyrolysis components were 1-phenanthrenecarboxylic acid, 1,2,3,4,4a,9,10,10a-octahydro-1,4a-dimethyl-7-(1-methylethyl)- ( 23.58%), ergosta-4,6,22-trien- 3.alpha.-ol(6.27%), decanoic acid, 1,2,3

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Bhat, Sujata V., Rohan S. Pawar, and P. Rajakannu. "Facile One-Pot Synthesis and Crystal Structure of 2:1 Adducts of Myrcene (or Ocimene) with Benzoquinones." Letters in Organic Chemistry 17, no. 8 (2020): 624–27. http://dx.doi.org/10.2174/1570178617666200227110001.

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One-pot tandem oxidation and double Diels-Alder reaction of myrcene or ocimene with in situ generated 1,4-benzoquinone or 1,2-benzoquinone at 0°C for 1.5 h yielded polyalkylated 1,4,4a,5,8,8a,9a,10a-octahydro-9,10-anthracenediones and bis(alkylated) 9,10-phenanthrenedione respectively. The structure of novel bis-adduct from ocimene, (1R,4aR,5S,8aS,9aS,10aR)-rel- 1,4,4a,5,8,8a,9a,10a-octahydro-2,6-dimethyl-1,5-bis(3-methyl-2-buten-1-yl)-9,10-anthracenedione, was elucidated through single crystal X-ray analysis.

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Purwati, Purwati, and Sabirin Matsjeh. "ANALISIS KOMPONEN KIMIA EKSTRAK METANOL FRAKSI PETROLEUM ETER DAUN EUPATORIUM ODORATUM DENGAN GC-MS." Molekul 3, no. 1 (2008): 10. http://dx.doi.org/10.20884/1.jm.2008.3.1.41.

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The purpose of this investigation was to analize the organic compounds of Eupatorium odoratum leaf and identification of the compounds using Gas Chromatography Mass Spectrometry (GC-MS). The sample was soaked in metanol. The extract of metanol was partitioned using petroleum ether. The extracts obtained were analyzed and identified by GC-MS. The results showed that in the extract of petroleum ether contained the organic compounds: germacrene, isocaryophyllene, 2,6,6,9-tetramethyl-1,4,8-cycloundecatriene, 1-methyl-5-methylene-8-(1-methylethyl)-1,7-cyclodecadiene, 1,2,4a,5,8,8a-hexahydro-4,7-dim

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Li-Zhulanov, Nikolai, Alexandra Zakharenko, Arina Chepanova, et al. "A Novel Class of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors That Contains the Octahydro-2H-chromen-4-ol Scaffold." Molecules 23, no. 10 (2018): 2468. http://dx.doi.org/10.3390/molecules23102468.

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Tyrosyl-DNA phosphodiesterase 1 (Tdp1) is a DNA repair enzyme that mends topoisomerase 1-mediated DNA damage. Tdp1 is a current inhibition target for the development of improved anticancer treatments, as its inhibition may enhance the therapeutic effect of topoisomerase 1 poisons. Here, we report a study on the development of a novel class of Tdp1 inhibitors that is based on the octahydro-2H-chromene scaffold. Inhibition and binding assays revealed that these compounds are potent inhibitors of Tdp1, with IC50 and KD values in the low micromolar concentration range. Molecular modelling predicte

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Griffiths, D. Vaughan, and Geoffrey Wilcox. "Synthetic and stereochemical studies of the octahydro-1-benzopyran system." Journal of the Chemical Society, Perkin Transactions 2, no. 4 (1988): 431. http://dx.doi.org/10.1039/p29880000431.

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Blinokhvatov, A. F., O. V. Markovtseva, S. V. Chivokin, et al. "Molecular complexes ofsym-octahydro-1-chalcogenaanthracene salts with aromatic compounds." Chemistry of Heterocyclic Compounds 31, no. 1 (1995): 23–27. http://dx.doi.org/10.1007/bf01171284.

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Mansur, Muhammad Abdullah Al, M. Mahboob Ali Siddiqi, Md Ahedul Akbor, and Koushik Saha. "Phytochemical Screening and GC-MS Chemical Profiling of Ethyl Acetate Extract of Seed and Stem of Anethum sowa Linn." Dhaka University Journal of Pharmaceutical Sciences 16, no. 2 (2018): 187–94. http://dx.doi.org/10.3329/dujps.v16i2.35256.

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Tahe phytochemical constituents from the ethyl acetate extracts of seed and stem of Anethum sowa were identified by qualitative and gas chromatography-mass spectroscopy (GC-MS). Qualitative analyses exhibited the presence of alkaloids, flavonoids, tannins, carbohydrate, steroids and terpenoids in both extracts. In GC-MS analysis of A. sowa 6 notable peaks (3,4,4a,5,6,7,8,9-Octahydro-2H-benzocyclohepten-2-one, 2,2,4,6,7-Pentamethyl- 1,2,3,4-tetrahydro quinoline, 5-Ethyl-2-methyl-pyridin-4-amine, 2-(2-Furyl) pyridine, 9-Ethyl 9-borabicyclo-[3.3.1]- nonane and 7-Methylenebicyclo-[4.2.0]-octane) a

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Bourke, David G., and David J. Collins. "The Conversion of Steroidal Ring B Lactones into Ortho Esters: Preparation of 7,7-Dimethoxy-6-oxaestra-1,3,5(10)-triene Derivatives." Australian Journal of Chemistry 51, no. 11 (1998): 1003. http://dx.doi.org/10.1071/c97179.

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17β-t-Butyldimethylsilyloxy-3-methoxy-6-oxaestra-1,3,5(10)-trien-7-one (1), prepared in three steps from 17b-hydroxy-3-methoxy-6-oxaestra-1,3,5(10),8-tetraen-7-one (5a), was converted via the corresponding phenolic acid into 1β-t-butyldimethylsilyloxy-5β-(2′-t-butyldimethylsilyloxy-4′-methoxyphenyl)-N,7aβ-dimethyl-N-phenyl-2,3,3aα,4,5,6,7,7a-octahydro-1H-indene-4α-carboxamide (17c). Subjection of (17c) to a reaction sequence with methyl trifluoromethanesulfonate, sodium methoxide/methanol, and then dry methanol/acetic acid gave a low yield (12%) of the ortho ester 3,7,7,17β-tetramethoxy- 6-oxa

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Schloegla, Martin, Carsten Trolla, Ulf Thewaltb, and Bernhard Riegera. "Semi-Hydrogenated, Asymmetric Metallocene Catalysts for the Propylene Polymerization." Zeitschrift für Naturforschung B 58, no. 6 (2003): 533–38. http://dx.doi.org/10.1515/znb-2003-0608.

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The hydrogenation of rac-[1-(9-η5-fluorenyl)-2-(5,6-cylopenta-2-methyl-1-η5-indenyl)ethane] metallocene dichlorides (1a: Zr, 1b: Hf) with PtO2/H2O/H2 is reported. The diastereoselective formation of exclusively rac-[1-(2,3,4,5,6,7,8,9-octahydro-η5-fluorenyl)-2-(2-methyl- 1,4,4a(R;S),5,6,7,7a(S;R),8-octahydro-s-η5-indacenyl)ethane]metallocene dichlorides (2a: Zr, 2b: Hf) was shown by 1H-NMR and by X-ray analysis of 2a. Both compounds were activated in situ with triisobutylaluminum/PhC+3 [B(C6F5)4]D and tested as catalysts in propylene polymerization reactions. Comparison to the non-hydrogenated

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Dissertations / Theses on the topic "Octahydro-1"

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Schrack-Belschner, Sonja Miriam Irmgard [Verfasser], and Wolfgang [Akademischer Betreuer] Schwack. "Determination of potentially hazardous oxidation products in cosmetics containing lanolin or 1-(1,2,3,4,5,6,7,8-octahydro-2,3,8,8-tetramethyl-2-naphthalenyl)ethanone (OTNE) / Sonja Miriam Irmgard Schrack-Belschner ; Betreuer: Wolfgang Schwack." Hohenheim : Kommunikations-, Informations- und Medienzentrum der Universität Hohenheim, 2019. http://d-nb.info/1201411041/34.

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Schrack-Belschner, Sonja [Verfasser], and Wolfgang [Akademischer Betreuer] Schwack. "Determination of potentially hazardous oxidation products in cosmetics containing lanolin or 1-(1,2,3,4,5,6,7,8-octahydro-2,3,8,8-tetramethyl-2-naphthalenyl)ethanone (OTNE) / Sonja Miriam Irmgard Schrack-Belschner ; Betreuer: Wolfgang Schwack." Hohenheim : Kommunikations-, Informations- und Medienzentrum der Universität Hohenheim, 2019. http://d-nb.info/1201411041/34.

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Carré, Christiane. "Étude des réactions photoinduites de l'octahydro-1,2,3,4,6,7,8,9 phénazine en solution ou la voie des diazines vers la photo-homolyse de l'eau." Paris 11, 1985. http://www.theses.fr/1985PA112084.

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Certaines diazines-1,4 - en particulier la phénazine – sont susceptibles de provoquer la photo-homolyse de l’eau. Ce travail porte sur les réactions photoinduites de l’octahydro-1,2,3,4,6,7,8,9 phénazine. Après étude par R. P. E. Des diverses espèces radicalaires formées par transfert d’un électron sur cette molécule, nous avons pu montrer que par irradiation des solutions d’octahydrophénazine dans l’eau ou dans l’alcool, c’est le radical cation qui se forme très rapidement : il résulte de l’arrachement d’un atome d’hydrogène par la molécule monoprotonée excitée. C’est surtout l’octahydrophéna

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Chen, Chien-Wen, та 陳建文. "Intramolecular Radical Cyclization Of α-Enone Radical: Synthesis Of 3,4,5a,6,7,8,9,9a-Octahydro-1(2H)dibenzofuranone". Thesis, 1994. http://ndltd.ncl.edu.tw/handle/62887520492245793540.

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Chang, Chun-Wei, and 張鈞崴. "1. Organocatalytic Enantioselective Synthesis of Steroid Skeleton 2. One-pot Synthesis of Racemic Octahydro-1H-indene Derivatives via Double Michael-Henry Reaction." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/00149832229969255903.

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碩士<br>國立中正大學<br>化學暨生物化學研究所<br>103<br>Asymmetric synthesis of highly enantioselective steroid skeleton with six stereogenic centers has been achieved by a sequential organocatalyzed Michael-Michael-aldol condensation and Henry reaction with nitroalkane and α,β-unsaturated aldehyde. In addition, different one-pot strategies were employed to optimize the yield. Furthermore, reaction of 2-methylcyclopentane-1,3-dione and trans-β-nitrostyrenes with base affect the indane derivatives via a Michael-Michael-Henry cascade.

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Book chapters on the topic "Octahydro-1"

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of vanadyl complex with Schiff-base derived from 1,2,3,5,6,7,8,8a-octahydro-3-oxo-N,1-diphenyl-5(phenylmethylene)-2-naphthalenecarboxamide and o-aminophenol." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_85.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of vanadyl complex with Schiff-base derived from 1,2,3,5,6,7,8,8a-octahydro-3-oxo-N,1-diphenyl-5(phenyl-methylene)-2-naphthalenecarboxamide and o-aminothiophenol." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_86.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mononuclear cobalt(II) complex with Schiff-base derived from 1,2,3,5,6,7,8,8a-octahydro-3-oxo-N,1-diphenyl-5(phenylmethylene)-2-naphthalenecarboxamide and o-aminophenol." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_480.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of vanadyl complex with Schiff-base derived from 1,2,3,5,6,7,8,8a-octahydro-3-oxo-N,1-diphenyl-5(phenyl-methylene)-2-naphthalenecarboxamide and o-aminobenzoic acid." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_87.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear copper(II) chloro complex with Schiff-base derived from 1,2,3,5,6,7,8,8a-octahydro-3-oxo-N,1-diphenyl-5(phenylmethylene)-2-naphthalenecarboxamide and o-aminophenol." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_473.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear copper(II) chloro complex with Schiff-base derived from 1,2,3,5,6,7,8,8a-octahydro-3-oxo-N,1-diphenyl-5(phenylmethylene)-2-naphthalenecarboxamide and o-aminothiophenol." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_474.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mononuclear cobalt(II) complex with Schiff-base derived from 1,2,3,5,6,7,8,8a-octahydro-3-oxo-N,1-diphenyl-5(phenyl-methylene)-2-naphthalenecarboxamide and o-aminothiophenol." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54231-6_481.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mononuclear nickel(II) chloro complex with Schiff-base derived from 1,2,3,5,6,7,8,8a-octahydro-3-oxo-N,1-diphenyl-5(phenylmethylene)-2-naphthalenecarboxamide and o-aminophenol." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_174.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of mononuclear nickel(II) complex with Schiff-base derived from 1,2,3,5,6,7,8,8a-octahydro-3-oxo-N,1-diphenyl-5(phenyl-methylene)-2-naphthalenecarboxamide and o-aminothiophenol." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54234-7_175.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of dinuclear copper(II) complex with Schiff-base derived from 1,2,3,5,6,7,8,8a-octahydro-3-oxo-N,1-diphenyl-5(phenyl-methylene)-2-naphthalenecarboxamide and o-aminobenzoic acid." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54237-8_475.

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Conference papers on the topic "Octahydro-1"

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Wemhoff, Aaron P., Alan K. Burnham, Albert L. Nichols, and Jaroslaw Knap. "Calibration Methods for the Extended Prout-Tompkins Chemical Kinetics Model and Derived Cookoff Parameters for RDX, HMX, LX-10 and PBXN-109." In ASME/JSME 2007 Thermal Engineering Heat Transfer Summer Conference collocated with the ASME 2007 InterPACK Conference. ASMEDC, 2007. http://dx.doi.org/10.1115/ht2007-32279.

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Thermal explosions result when local temperature-dependent heat generation exceeds heat loss via conduction. The temperature dependence of the heat source term is directly related to the material’s chemical kinetics, and hence the chemical kinetics has a direct impact on the thermal explosion times of a material. Much success has been gained in past work to accurately model thermal explosions in various explosives using multi-step Arrhenius chemical kinetics models. However, the generation of these kinetics models is time consuming and complex. Therefore, a methodology has been developed that

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Reports on the topic "Octahydro-1"

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Bausum, Howard T. Recommended Water Quality Criteria for Octahydro-1,3,5,7-Tentranitro-1, 3,5,7-Tetrazocin (HMX). Defense Technical Information Center, 1989. http://dx.doi.org/10.21236/ada258561.

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