Relevant bibliographies by topics / Absolute stereochemistry

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Absolute stereochemistry'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "Absolute stereochemistry"

1

Hu, Yulin, Herman Ziffer, and J. V. Sllverton. "Preparation and absolute stereochemistry of (−)-acenaphthenol." Canadian Journal of Chemistry 67, no. 1 (1989): 60–62. http://dx.doi.org/10.1139/v89-010.

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1-Acenaphthenol was resolved by fractional crystallization of its camphanate ester followed by hydrolysis. The absolute stereochemistry of the (+)-camphanate and (−)-alcohol, derived therefrom, was established as (R) by X-ray crystallography. Keywords: (−)-acenaphthenol, stereochemistry, synthesis, X-ray crystallography.
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2

Hayashi, Ken-ichiro, Masahira Nakagawa, Tomoyuki Fujita, and Mitsuru Nakayama. "Absolute Stereochemistry of Alisamycin." Bioscience, Biotechnology, and Biochemistry 58, no. 7 (1994): 1332–33. http://dx.doi.org/10.1271/bbb.58.1332.

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Cui, Zheng, Ping Zhu, Masayuki Onda, et al. "Absolute Stereochemistry of (-)-Ambinine." Journal of Natural Products 53, no. 5 (1990): 1182–86. http://dx.doi.org/10.1021/np50071a008.

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Takahashi, Yohei, Takaaki Kubota, Eri Fukushi, Jun Kawabata, and Jun’ichi Kobayashi. "Absolute Stereochemistry of Amphidinolide Q." Organic Letters 10, no. 17 (2008): 3709–11. http://dx.doi.org/10.1021/ol8013123.

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Ungur, Nicon, Margherita Gavagnin, Ernesto Mollo, and Guido Cimino. "Absolute stereochemistry of anisodorin 5." Tetrahedron: Asymmetry 10, no. 9 (1999): 1635–36. http://dx.doi.org/10.1016/s0957-4166(99)00160-3.

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Al Dulayymi, Juma'a R., Mark S. Baird, and Keith Jones. "The absolute stereochemistry of grenadamide." Tetrahedron 60, no. 2 (2004): 341–45. http://dx.doi.org/10.1016/j.tet.2003.11.006.

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Sarma, J. C., R. P. Sharma, R. De Jong, and C. H. Stam. "Absolute stereochemistry of tagitinin A." Phytochemistry 26, no. 8 (1987): 2406–7. http://dx.doi.org/10.1016/s0031-9422(00)84732-9.

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Ishibashi, Masami, Haruaki Ishiyama, and Jun'ichi Kobayashi. "Absolute stereochemistry of amphidinolide B." Tetrahedron Letters 35, no. 44 (1994): 8241–42. http://dx.doi.org/10.1016/0040-4039(94)88292-4.

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Allingham, John S., Junichi Tanaka, Gerard Marriott, and Ivan Rayment. "Absolute Stereochemistry of Ulapualide A." Organic Letters 6, no. 4 (2004): 597–99. http://dx.doi.org/10.1021/ol036458y.

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Kubota, Takaaki, Masashi Tsuda, and Jun'ichi Kobayashi. "Absolute Stereochemistry of Amphidinolide E." Journal of Organic Chemistry 67, no. 5 (2002): 1651–56. http://dx.doi.org/10.1021/jo016326n.

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Dissertations / Theses on the topic "Absolute stereochemistry"

1

Kennedy, D. A. "Crystallographic studies of relative and absolute stereochemistry." Thesis, Queen's University Belfast, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.373533.

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Turner, Helen Louise. "Absolute stereochemistry : the merits of VCD and XRD." Thesis, University of Southampton, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.430715.

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Roberts, Ieuan Owain. "The absolute stereochemistry of various naturally occurring fatty acids." Thesis, Bangor University, 2006. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.429867.

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O'Loughlin, Julian Matthew Adrian. "Control of absolute stereochemistry in the aza-(2,3)-Wittig rearrangement." Thesis, University of Nottingham, 2004. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.415867.

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Dorrity, Michael R. J. "Crystallographic studies of relative and absolute stereochemistry in cycloadducts and arene metabolites." Thesis, Queen's University Belfast, 1992. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.317502.

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Evans, Timothy Arthur. "Crystallographic studies of relative and absolute stereochemistry in substituted arenes and arene metababolites." Thesis, Queen's University Belfast, 1994. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.241391.

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MacMillan, John Bryan. "Investigation of the diverse secondary metabolism of cyanobacteria : structural elucidation and absolute stereochemistry /." For electronic version search Digital dissertations database. Restricted to UC campuses. Access is free to UC campus dissertations, 2004. http://uclibs.org/PID/11984.

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Sun, Han. "Stereochemistry of Challenging Natural Products Studied by NMR-based Methods." Doctoral thesis, Niedersächsische Staats- und Universitätsbibliothek Göttingen, 2012. http://hdl.handle.net/11858/00-1735-0000-000D-FD1A-F.

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Pedroso, Marcelo. "Caleol: modificações estruturais, estereoquímica absoluta e atividade antimicrobiana dos derivados." Universidade Federal de Santa Maria, 2011. http://repositorio.ufsm.br/handle/1/10488.

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Conselho Nacional de Desenvolvimento Científico e Tecnológico<br>The essential oil of the leaves of Calea clematidea, a plant of Asteraceae family used in the folk medicine in treatment of flu, stomachic disease and gastric ulcer, was extracted and of it was isolated the monoterpene caleol. This metabolite was submitted to structural modification reactions by the opening of its epoxide functional group. In the reactions catalyzed by anhydrous iron (III) chloride, the epoxide opening was selective when primary alcohols was used like nucleophile, giving like product the less substituted alcohol.
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Tennant, Shaun. "Chiral biaryls : the absolute configuration of streptonigrin." Phd thesis, 1992. http://hdl.handle.net/1885/140167.

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Books on the topic "Absolute stereochemistry"

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1951-, Hill R. A., and Klyne William, eds. Atlas of stereochemistry, absolute configurations of organie molecules, second edition. Chapman and Hall, 1986.

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2

Reddy, Guvvala Nagabhushana. Absolute stereochemistry and total synthesis of botryococcene. 1987.

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3

Kennedy, Deirdre Anne. Crystallographic studies of relative and absolute stereochemistry. 1985.

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4

Atlas of Stereochemistry: Absolute Configurations of Organic Molecules. Chapman & Hall, 1987.

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Book chapters on the topic "Absolute stereochemistry"

1

Saito, Yoshihiko. "Absolute Stereochemistry of Chelate Complexes." In Topics in Stereochemistry. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470147191.ch2.

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Krow, Grant. "The Determination of Absolute Configuration of Planar and Axially Dissymmetric Molecules." In Topics in Stereochemistry. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470147146.ch2.

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Harada, Nobuyuki. "Chiral Auxiliaries Powerful for Both Enantiomer Resolution and Determination of Absolute Configuration by X-Ray Crystallography." In Topics in Stereochemistry. John Wiley & Sons, Inc., 2006. http://dx.doi.org/10.1002/0471785156.ch6.

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Addadi, L., Z. Berkovitch-Yellin, I. Weissbuch, M. Lahav, and L. Leiserowitz. "A Link Between Macroscopic Phenomena and Molecular Chirality: Crystals as Probes for the Direct Assignment of Absolute Configuration of Chiral Molecules." In Topics in Stereochemistry. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470147252.ch1.

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Manstein, D. J., V. Massey, and E. F. Pai. "Absolute stereochemistry of flavins in enzyme - catalyzed reactions." In Flavins and Flavoproteins 1987, edited by D. E. Edmondson and D. B. McCormick. De Gruyter, 1987. http://dx.doi.org/10.1515/9783110884715-004.

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Harada, Nobuyuki, and Shunsuke Kuwahara. "CD Spectra of Chiral Extended π-Electron Compounds: Theoretical Determination of the Absolute Stereochemistry and Experimental Verification." In Comprehensive Chiroptical Spectroscopy. John Wiley & Sons, Inc., 2012. http://dx.doi.org/10.1002/9781118120392.ch5.

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"Absolute Configuration." In Stereochemistry and Stereoselective Synthesis: An Introduction. Wiley-VCH Verlag GmbH & Co. KGaA, 2017. http://dx.doi.org/10.1002/9783527341177.ch4.

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Seco, J. M., and R. Riguera. "Absolute Stereochemistry by NMR Spectroscopy." In Encyclopedia of Spectroscopy and Spectrometry. Elsevier, 2017. http://dx.doi.org/10.1016/b978-0-12-409547-2.12115-8.

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Robinson, Michael J. T. "Racemates and resolution." In Organic Stereochemistry. Oxford University Press, 2000. http://dx.doi.org/10.1093/hesc/9780198792758.003.0005.

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This chapter extends the concept of stereoisomerism to groups of molecules, e.g., in crystals, or a molecule surrounded by a solvent or adsorbed on a surface. It argues that these are essential in some methods for resolving racemic compounds, i.e., separating mixtures of enantiomeric compounds. The chapter also discusses the scalar properties in terms of interatomic distances and energies. It notes that these are independent of the absolute configuration of a chiral molecule that is either isolated or in an achiral environment. The chapter then jumps to investigate how enantiomeric chiral mole
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Bansal, Anshul. "Stereochemistry of Organic Compounds-II." In Basics of Organic Chemistry: A Textbook for Undergraduate Students. BENTHAM SCIENCE PUBLISHERS, 2024. http://dx.doi.org/10.2174/9789815223224124010007.

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This chapter continues the exploration of stereochemistry in organic compounds, focusing on detailed methods for describing and differentiating the spatial arrangement of atoms within molecules. It begins with absolute configuration, which provides a precise description of the spatial arrangement of atoms around a chiral center, independent of other molecules. Relative configuration is then discussed, explaining how the arrangement of atoms in one chiral molecule relates to another, often determined through chemical interconversion. The D-L system, a traditional method for denoting configurati
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Conference papers on the topic "Absolute stereochemistry"

1

Bešlo, D., M. Molnar, D. Agić, S. Roca, and B. Lučić. "THE PREDICTION ACCURACY OF 1H AND 13C NMR CHEMICAL SHIFTS OF COUMARIN DERIVATIVES BY CHEMO/BIOINFORMATICS METHODS." In 1st INTERNATIONAL Conference on Chemo and BioInformatics. Institute for Information Technologies, University of Kragujevac, 2021. http://dx.doi.org/10.46793/iccbi21.422b.

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In plant biochemistry and physiology, coumarins are known as antioxidants, enzyme inhibitors and precursors of toxic substances. Nuclear magnetic resonance (NMR) spectra are primary sources of molecular structural data. NMR provides detailed information about the local environment of the atom which can be used to determine the atomic connectivity, stereochemistry, and molecular conformation. For many years the molecular structure has been determined by NMR spectroscopy and chemical shifts are determined manually with the help of computer programs. However, recent progress in computational chem
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Reports on the topic "Absolute stereochemistry"

1

สุวรรณบริรักษ์, คณิต, та สุรัตนา อำนวยผล. การศึกษาทางพฤกษเคมีของต้นข้าวหลาม : รายงานผลการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 1996. https://doi.org/10.58837/chula.res.1996.14.

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ได้ทำการสกัดแยกสารจากเปลือกต้นข้าวหลาม Goniothalamus marcanii Craib โดยใช้วิธีทางโครมาโทกราฟีควบคู่ไปกับผลการทดสอบฤทธิ์ทางชีวภาพ ทำให้สามารถแยกสารได้ 4 กลุ่ม โดยการวิเคราะห์ข้อมูลจากสเปกโทรสโกปีเพื่อพิสูจน์สูตรโครงสร้างทางเคมีของสารที่แยกได้ ทำให้ทราบว่าสารทั้ง 4 กลุ่มคือ 1-azaanthraquinones, flavanoids, triterpenoids และ mono-THF annonaceous acetogenins โดยที่สารกลุ่ม 1-azaanthraquinoes ที่แยกได้เป็นสารชนิดใหม่ 1 ชนิด คือ marcanine C ร่วมกับสารที่ทราบสูตรโครงสร้างแล้ว 2 ชนิด คือ marcanine A และ dielsiquinone ส่วนสารกลุ่ม flavanoids ที่แยกได้เป็นสารที่ทราบสูตรโครงสร้างแล้ว 1 ชนิด คือ pinocembr
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