Добірка наукової літератури з теми "Decalones"
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Статті в журналах з теми "Decalones"
Huffman, John W., and William H. Balke. "Enolization of 2-decalones." Journal of Organic Chemistry 53, no. 16 (August 1988): 3828–31. http://dx.doi.org/10.1021/jo00251a030.
Повний текст джерелаJ. Hart, David, and Shung C. Wu. "Gelsemine Model Studies: Alkoxymethylations of Decalones and Indoles." HETEROCYCLES 35, no. 1 (1993): 135. http://dx.doi.org/10.3987/com-92-s57.
Повний текст джерелаSuh, Young-Ger, Hwa-Soon Kim, P. Raja kumar, Nam-Song Choi, and Jae-Kyung Jung. "Practical and versatile syntheses of angular hydroxymethylated decalones." Tetrahedron 54, no. 50 (December 1998): 15161–66. http://dx.doi.org/10.1016/s0040-4020(98)00965-x.
Повний текст джерелаFerraz, Helena M. C., and Luiz F. Silva Jr. "Thallium trinitrate mediated ring contraction of cis-2-decalones." Journal of the Brazilian Chemical Society 12, no. 4 (August 2001): 548–51. http://dx.doi.org/10.1590/s0103-50532001000400018.
Повний текст джерелаSolladié-Cavallo, Arlette, Loïc Jierry, Arlette Klein, Michel Schmitt та Richard Welter. "α-Fluoro decalones as chiral epoxidation catalysts: fluorine effect". Tetrahedron: Asymmetry 15, № 24 (грудень 2004): 3891–98. http://dx.doi.org/10.1016/j.tetasy.2004.10.033.
Повний текст джерелаPiriou, Francois, and Hugues d'Orchymont. "Synthesis and Conformational Analysis of 3-Amino-2-decalones." Magnetic Resonance in Chemistry 34, no. 3 (March 1996): 213–20. http://dx.doi.org/10.1002/(sici)1097-458x(199603)34:3<213::aid-omr868>3.0.co;2-a.
Повний текст джерелаSuh, Young-Ger, Hwa-Soon Kim, P. Raja Kumar, Nam-Song Choi, and Jae-Kyung Jung. "ChemInform Abstract: Practical and Versatile Syntheses of Angular Hydroxymethylated Decalones." ChemInform 30, no. 17 (June 16, 2010): no. http://dx.doi.org/10.1002/chin.199917108.
Повний текст джерелаHART, D. J., and S. C. WU. "ChemInform Abstract: Gelsemine Model Studies: Alkoxymethylations of Decalones and Indoles." ChemInform 24, no. 29 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199329175.
Повний текст джерелаZiegler, Frederick E., Ki Jun Hwang, John F. Kadow, Scott I. Klein, Uttam K. Pati, and Tein Fu Wang. "Practical routes to two functionalized decalones for the synthesis of quassinoids." Journal of Organic Chemistry 51, no. 24 (November 1986): 4573–79. http://dx.doi.org/10.1021/jo00374a016.
Повний текст джерелаAn, Yi Zhong, and David F. Wiemer. "Regiochemistry of vinyl phosphate/.beta.-keto phosphonate rearrangements in functionalized cyclohexanones and decalones." Journal of Organic Chemistry 57, no. 1 (January 1992): 317–21. http://dx.doi.org/10.1021/jo00027a055.
Повний текст джерелаДисертації з теми "Decalones"
Crews, Everett III. "Retroaldo-trapping reactions of [beta]-hydroxy-[alpha]-phenylsulfenyl cyclohexanone and decalone derivatives and the total synthesis of the California red scale sex pheromone." Diss., Georgia Institute of Technology, 1985. http://hdl.handle.net/1853/27404.
Повний текст джерелаBeer, Leilani. "The role of the priests in Israelite identity formation in the exilic/post-exilic period with special reference to Leviticus 19:1-19a." Thesis, 2021. http://hdl.handle.net/10500/27842.
Повний текст джерелаSource-criticism of the Pentateuch suggests that the priests (Source P) alone authored the Holiness Code – the premise being that Source P forms one religious, literate and elite group of several. Through the endeavor to redefine Israelite identity during the Neo-Babylonian Empire of 626–539 BCE and the Achaemenid Persian Empire of 550–330 BCE, various ideologies of Israelite identity were produced by various religious, literate and elite groups. Possibly, the Holiness Code functions as the compromise reached between two such groups, these being: the Shaphanites, and the Zadokites. Moreover, the Holiness Code functions as the basis for the agreed identity of Israel as seen by the Shaphanites and the Zadokites. Specifically, in Leviticus 19:1-19a – as being the Levitical decalogue of the Holiness Code, and which forms the emphasis of this thesis – both Shaphanite and Zadokite ideologies are expressed therein. The Shaphanite ideology is expressed through the Mosaic tradition: i.e., through the Law; and the Zadokite ideology is expressed through the Aaronide tradition: i.e., through the Cult. In the debate between the supremacy of the Law, or the Cult – i.e., Moses or Aaron – the ancient Near Eastern convention of the ‘rivalry between brothers’ is masterfully negotiated in Leviticus 19:1-19a.
Old Testament and Ancient Near Eastern Studies
D. Phil. (Old Testament)
Книги з теми "Decalones"
Cai, Edward Yi-Gu. Approaches to the synthesis of 9-hydroxy-4,10-dimethyl-1-decalones. Ottawa: National Library of Canada, 1990.
Знайти повний текст джерелаLuther, Martin. Solus Decalogus est aeternus =: Martin Luther's complete antinomian theses and disputations. Minneapolis, MN: Lutheran Press, 2008.
Знайти повний текст джерелаCarmichael, Calum M. The origins of Biblical law: The Decalogues and the Book of the Covenant. Ithaca, N.Y: Cornell University Press, 1992.
Знайти повний текст джерелаADAMS, John. Fesarius: The Decalon Trap. Independently Published, 2020.
Знайти повний текст джерелаScarbrough, Allen L. Rise and Fall of Man: Decalogues-Book One. Lulu Press, Inc., 2012.
Знайти повний текст джерелаOrtiz, Carlos Alberto Rendon. 69, Mejor, 72 Historias Cortas de Salud y Seguridad en el Trabajo: Decalogos Del Jefe y Del Lider en Caso de Accidente. Independently Published, 2018.
Знайти повний текст джерелаЧастини книг з теми "Decalones"
"1. The Decalogues." In The Origins of Biblical Law, 22–73. Ithaca, NY: Cornell University Press, 2020. http://dx.doi.org/10.7591/9781501733666-004.
Повний текст джерелаТези доповідей конференцій з теми "Decalones"
Caliebe, Swantje, Melanie Schnell, and Pablo Pinacho. "INTERPLAY OF INTERMOLECULAR INTERACTIONS: COMPLEXES OF 2-DECALONE WITH WATER, BENZENE, AND PHENOL." In 2022 International Symposium on Molecular Spectroscopy. Urbana, Illinois: University of Illinois at Urbana-Champaign, 2022. http://dx.doi.org/10.15278/isms.2022.fd02.
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