Relevant bibliographies by topics / Heneicosene

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Heneicosene'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Heneicosene"

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ARUN, SABHARWAL, SHARMA SANJIV, VIG RAKESH, BHATTI B.S., and SHARMA S.C. "Short Synthesis of (Z)-7-Heneicosene and (Z)-7-Tricosene." Journal of Indian Chemical Society Vol. 66, Jun 1989 (1989): 411–12. https://doi.org/10.5281/zenodo.6140766.

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Department of Chemistry, Panjab University,&nbsp;Chandigarh-160 014 Department of Chemistry, H. P. University, Shimla <em>Manuscript&nbsp;received 31 October 1988, accepted 31&nbsp;March 1989</em> Short Synthesis of (Z)-7-Heneicosene and (Z)&middot;7-Tricosene&nbsp;
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EBATA, Takashi, and Kenji MORI. "Synthesis of both the enantiomers of (Z)-cis-9,10-epoxy-6-heneicosene." Agricultural and Biological Chemistry 53, no. 3 (1989): 801–4. http://dx.doi.org/10.1271/bbb1961.53.801.

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Ebata, Takashi, and Kenji Mori. "Synthesis of Both the Enantiomers of (Z)-cis-9,10-Epoxy-6-heneicosene." Agricultural and Biological Chemistry 53, no. 3 (1989): 801–4. http://dx.doi.org/10.1080/00021369.1989.10869343.

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Gries, R., D. Holden, G. Gries, P. D. C. Wimalaratne, K. N. Slessor, and C. Saunders. "3Z-cis-6,7-cis-9,10-Di-epoxy-heneicosene: Novel Class of Lepidopteran Pheromone." Naturwissenschaften 84, no. 5 (1997): 219–21. http://dx.doi.org/10.1007/s001140050383.

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Battu, Raminderjit S., Ranjit S. Dhillon, and Jasvinder Singh. "ChemInform Abstract: Synthesis of (Z)-7-Heneicosene and (Z)-7-Tricosene via Organoboranes. Part 5." ChemInform 31, no. 10 (2010): no. http://dx.doi.org/10.1002/chin.200010234.

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Gözcü, Sefa, Zeynep Akşit, and Hüseyin Akşit. "Antimicrobial Activity and Chemical Composition of Essential Oil Extracted from Hyoscyamus niger L. Inflorescence." Erzincan Üniversitesi Fen Bilimleri Enstitüsü Dergisi 17, no. 3 (2024): 751–60. https://doi.org/10.18185/erzifbed.1522296.

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This study aimed to analyze the chemical composition and evaluate the antibacterial activity of essential oils extracted from the H. niger inflorescence collected from Erzincan, Türkiye. The essential oils were extracted using hydrodistillation and analyzed by GC-MS, identifying 23 components, with major constituents being 10-heneicosene (35.72%), phytol (20.50%), and acetic acid, butyl ester (10.10%). The antibacterial activity was tested against six bacterial strains, including Staphylococcus aureus, Clostridium perfringens, Enterococcus faecalis, Bacillus cereus, Listeria monocytogenes, and
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Kar, Dattatreya, Hiramanjari Barik, Ananya Kuanar, et al. "Gas chromatographic methods coupled to mass spectrometry detection of leaf extracts of Symplocos racemosa Roxb." Israel Journal of Plant Sciences 68, no. 4 (2021): 277–86. http://dx.doi.org/10.1163/22238980-bja10034.

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Abstract Symplocos racemosa Roxb., belonging to the family Symplocaceae, is an important medicinal plant. Chemometric profile of chloroform, methanol and ethanol leaf extracts of S. racemosa were performed by hyphenated gas chromatography mass spectrometry (GC/MS) technique. Chemometric profile of leaf extracts revealed the presence of 57 phyto-chemotypes, among them, Erucylamide (15.94%), Vitamin E (8.26%), 10-Heneicosene (8.97%), n-Hexadecanoic acid (5.21%), 1-Heneicosyl formate (5.11%), Tetracosanol (5.36%), 2,4-Hexanedione, 5,5-dimethyl- (11.94%), Linoleic acid (19.30%), Dibutyl phthalate
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Robustelli della Cuna, Francesco Saverio, Pierluigi Cortis, Fabiana Esposito, Antonio De Agostini, Cristina Sottani, and Cinzia Sanna. "Chemical Composition of Essential Oil from Four Sympatric Orchids in NW-Italy." Plants 11, no. 6 (2022): 826. http://dx.doi.org/10.3390/plants11060826.

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Orchidaceae is a flowering plant family worldwide distributed known for producing volatile organic compounds (VOCs) which can act as olfactory signals for pollinators. Despite the importance of VOCs in the different reproductive strategies, in the literature there are only a few publications on the characterization of orchids’ volatile profiles. In this study, the essential oils from fresh inflorescences of sympatric orchids Anacamptis morio, Himantoglossum robertianum, Ophrys sphegodes and Orchis purpurea, naturally growing in Piedmont (Italy) were isolated by steam distillation and character
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Erida, Gina, Nurdin Saidi, Hasanuddin Hasanuddin, and Syafruddin Syafruddin. "Herbicidal Effects of Ethyl Acetate Extracts of Billygoat Weed (Ageratum conyzoides L.) on Spiny Amaranth (Amaranthus spinosus L.) Growth." Agronomy 11, no. 10 (2021): 1991. http://dx.doi.org/10.3390/agronomy11101991.

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This study aimed to evaluate the herbicidal activity of ethyl acetate leaf extract of Ageratum conyzoides L. at different subfractions on Amaranthus spinosus L. The leaves of A. conyzoides were sequentially extracted with n-hexane and ethyl acetate respectively and fractionated by chromatography column. The extracts were applied to A. spinosus in pot assays at a concentration of 5%, 10% and 15%. We applied A synthetic herbicide (2,4-D at 0.686 kg a.i. ha−1) for positive control and distilled water for negative control. The A. conyzoides extracts strongly differed in their effect on weed contro
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Abo El-Fadl, Reda E., Mahmoud M. El-Saber, Manal E. A. Ahmed, Tamer M. Abd Elaziem, and Ahmed A. El-Sayed. "Impact on Growth and Secondary Metabolites in White Poplar (Populus alba L.) Callus using SeNPs@Moringa." Current Materials Science 15, no. 2 (2022): 175–91. http://dx.doi.org/10.2174/2666145414666211125093640.

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Background: Green synthesis of nanoparticles has provided a cost-effective, environmentally friendly method, as well as raised safe strategies for the synthesis of nanomaterials. Methods: In this study, we investigated the synthesis of Selenium nanoparticles from the leaf aqueous extract of Moringa oleifera (MO-SeNPs) and studied the effect of MO-SeNPs and Moringa extract with various concentrations on the growth, active constituents, and antioxidant activity (scavenging DPPH) of Populus alba callus. MS medium supplemented with (2, 4-D at 2 mg/l + 0.5 mg/l BA) took the maximum callus induction
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Dissertations / Theses on the topic "Heneicosene"

1

Waters, Stephen Joseph 1957. "In vivo and in vitro toxicity of M-741 (3,15 di-(5,5-dimethyl-3-N(-(cyclopropylmethylinium)-(N-propylinium));-1-cyclohex-1-enyl);-7,11,18,21-tetraoxa-3,15-diazatrispiro (5.2.2.5.2.2); heneicosane)." Diss., The University of Arizona, 1996. http://hdl.handle.net/10150/282154.

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M-741 (3,15 di-[5,5-dimethyl-3-N[-(cyclopropylmethylinium)-(N-propylinium]-1-cyclohex-1-enyl]-7,11,18,21-tetraoxa-3,15-diazatrispiro [5.2.2.5.2.2] heneicosane produces hepatotoxicity in rats following intravenous administration. Hepatocellular pathology is characterized by parenchymal cell necrosis and inflammatory cell infiltration. Electron microscopic evaluation could not identify any treatment-related effects on mitochondria or the production of cytoplasmic lysosomal lamellar bodies. The M-741-induced hepatotoxicity is not modified by manipulations of nutritional status (fasting), hepatic
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Weng, Chiu-Feng, та 翁垂豐. "The synthesis of 13-Oxa-hexacyclo[9.6.2.210,16.02,7.09,17.011,15]Heneicosan-2,4,18,20-tetra-en-3,6-dione and π-facial selectivity". Thesis, 2000. http://ndltd.ncl.edu.tw/handle/27882242083601429408.

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碩士<br>東海大學<br>化學系<br>88<br>Abstract Diels-Alder reaction of dienone 12 with p-benzoquinone produced ﹝4＋2﹞cycloadduct 17, which was then subjected to aromatization and then oxidation to give quinone 19. Cycloaddition of 19 with cyclopentadiene and dienone 12 produced a mixture of 21a/21b and 23a respectively. Structural analysis of these compounds showed that the Diels-Alder reaction of 19 gives highly π-facial selectivity. The cyclic dienes approached exclusively from the syn face relative to the etheno-bridges of 19. The cycloadduct 23a was subjected to aromatization and followed
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Book chapters on the topic "Heneicosene"

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"heneicosane, n." In Oxford English Dictionary, 3rd ed. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/4380117895.

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Chanu, Khomdram Utarani, and Dr Wangkheimayum Marjit Singh. "EXTRACTION, ISOLATION AND PURIFICATION OF PURE COMPOUNDS 3-METHYL-HENEICOSANE FROM MESOSPHAERUM SUAVEOLENS (LANCHAK) OF LAMIACEAE FAMILY." In Futuristic Trends in Agriculture Engineering & Food Sciences Volume 3 Book 5. Iterative International Publisher, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3bcag5p1ch3.

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A naturally occurring hydrocarbon 3-methyl-Heinecosane was isolated from the petroleum ether extract of the dry plant Mesosphaerum suaveolens (Lanchak) and was characterised by UV-Visible Spectroscopy, Fourier transforms infra red (FT-IR) spectroscopy, Nuclear Magnetic Resonance (NMR) and GC-Mass spectroscopy. The fragmentation ions with their m/z of compound 1, 3-methyl-Heineicosane were studied and all of the relative abundance found in the GC-MS spectra is in agreement.
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Journal articles
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