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Artykuły w czasopismach na temat "Carbocyclic ring compounds"
Yavari, Issa, i Aliyeh Khajeh-Khezri. "Recent Advances in the Synthesis of Hetero- and Carbocyclic Compounds and Complexes Based on Acenaphthylene-1,2-dione". Synthesis 50, nr 20 (16.08.2018): 3947–73. http://dx.doi.org/10.1055/s-0037-1610209.
Pełny tekst źródłaLautens, Mark, Dino Alberico, Cyril Bressy, Yuan-Qing Fang, Brian Mariampillai i Thorsten Wilhelm. "Palladium-catalyzed ring-forming reactions: Methods and applications". Pure and Applied Chemistry 78, nr 2 (1.01.2006): 351–61. http://dx.doi.org/10.1351/pac200678020351.
Pełny tekst źródłaBanwell, MG. "New Methods for the Synthesis of Troponoid Compounds". Australian Journal of Chemistry 44, nr 1 (1991): 1. http://dx.doi.org/10.1071/ch9910001.
Pełny tekst źródłaSaborit, Gisela V., Carlos Cativiela, Ana I. Jiménez, Josep Bonjoch i Ben Bradshaw. "Synthesis of cis-hydrindan-2,4-diones bearing an all-carbon quaternary center by a Danheiser annulation". Beilstein Journal of Organic Chemistry 14 (9.10.2018): 2597–601. http://dx.doi.org/10.3762/bjoc.14.237.
Pełny tekst źródłaHalliday, Jill I., Mary Chebib i Malcolm D. McLeod. "Synthesis and Biological Evaluation of a New Family of Constrained Azabicyclic Homocholine Analogues". Australian Journal of Chemistry 63, nr 5 (2010): 808. http://dx.doi.org/10.1071/ch10024.
Pełny tekst źródłaMikaia, Anzor. "Protocol for structure determination of unknowns by EI mass spectrometry. II. Diagnostic ions in one ring alicyclic, heterocyclic, and aromatic compounds". Journal of Physical and Chemical Reference Data 52, nr 2 (1.06.2023): 021501. http://dx.doi.org/10.1063/5.0140771.
Pełny tekst źródłaSivakrishna, Balija, Sehbanul Islam, Amarendra Panda, Maddi Saranya, Manas K. Santra i Shantanu Pal. "Synthesis and Anticancer Properties of Novel Truncated Carbocyclic Nucleoside Analogues". Anti-Cancer Agents in Medicinal Chemistry 18, nr 10 (23.01.2019): 1425–31. http://dx.doi.org/10.2174/1871520618666180322120533.
Pełny tekst źródłaTakahashi, Hidetoshi, Kazuhiro Yoshida i Akira Yanagisawa. "Synthesis of Carbocyclic Aromatic Compounds Using Ruthenium-Catalyzed Ring-Closing Enyne Metathesis". Journal of Organic Chemistry 74, nr 10 (15.05.2009): 3632–40. http://dx.doi.org/10.1021/jo900456g.
Pełny tekst źródłaPaquette, Leo A. "Book Review, Carbocyclic Three-Membered Ring Compounds, Houben-Weyl, Methods of Organic Chemistry". Synthesis 1998, nr 02 (luty 1998): 225. http://dx.doi.org/10.1055/s-1998-4511.
Pełny tekst źródłaPaquette, Leo A. "Book Review, Carbocyclic Four-Membered Ring Compounds, Houben-Weyl, Methods of Organic Chemistry". Synthesis 1998, nr 02 (luty 1998): 226. http://dx.doi.org/10.1055/s-1998-4512.
Pełny tekst źródłaRozprawy doktorskie na temat "Carbocyclic ring compounds"
Song, Eunho Krafft Marie E. "Ring-closing metathesis for the synthesis of carbocyclic and heterocyclic intramolecular Baylis-Hillman adducts". Diss., 2005. http://etd.lib.fsu.edu/theses/available/etd-05062005-172529.
Pełny tekst źródłaAdvisor: Dr. Marie E. Krafft, Florida State University, College of Arts and Sciences, Dept. of Chemistry and Biochemistry. Title and description from dissertation home page (viewed Sept. 19, 2005). Document formatted into pages; contains 147 pages. Includes bibliographical references.
Singh, Jatinder. "C-H activation and multi-functionalization of carbocyclic rings bound to the sandwich compound, (n5-RCp)Co(n4-C4Ph3R')". Thesis, 2017. http://localhost:8080/iit/handle/2074/7258.
Pełny tekst źródła"Synthetic studies of carbocycles from carbohydrates". Thesis, 2008. http://library.cuhk.edu.hk/record=b6074641.
Pełny tekst źródłaIn this thesis, a review regarding intramolecular direct aldol reaction from 1971 to 2008 is presented. The background information on pseudo-acarviosin, valiolamine and its containing compounds, gabosines and human glutathione transferase (hGST) is introduced.
Intramolecular direct aldol reaction was investigated for the construction of cyclohexanones and cycloheptanones from carbohydrates. Amine bases, amide bases and L-proline were employed to facilitate cyclization of 1,5- and 1,6-diketones successfully. These 1,5- and 1,6-diketones were prepared from carbohydrates by standard transformations. Different bases were employed to promote cyclization of 1,5-diketone derived from D-glucose to give cyclohexanones stereoselectively.
Intramolecular nitrile oxide-alkene cycloaddition (INOC) was studied with sugar derivatives having free hydroxyl groups. The INOC reaction, by incorporating chloramine-T and silica gel for the formation of nitrile oxide from oxime, proceeded smoothly with one, two, and four unmasked hydroxyl groups to give cyclopentanes and cyclohexanes.
The polyhydroxylated carbocycles constructed from sugars were successfully transformed into a variety of target molecules including pseudo-acarviosin, valiolamine and its containing compounds and gabosines. A series of 2-crotonyloxymethyl-(4 R,5R,6R)-4,5,6-trihydroxy-2-cyclohexenone (COTC) analogues as inhibitors of hGST were prepared in order to study the structure-activity relationships.
Cheng, Hau Man.
Adviser: Tony K. M. Shing.
Source: Dissertation Abstracts International, Volume: 70-06, Section: B, page: 3508.
Thesis (Ph.D.)--Chinese University of Hong Kong, 2008.
Includes bibliographical references (leaves 214-224).
Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web.
Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [200-] System requirements: Adobe Acrobat Reader. Available via World Wide Web.
Abstracts in English and Chinese.
School code: 1307.
"Construction of carbocycles from carbohydrates via 1,3-dipolar cycloadditions". 2007. http://library.cuhk.edu.hk/record=b5893442.
Pełny tekst źródłaThesis (M.Phil.)--Chinese University of Hong Kong, 2007.
Includes bibliographical references (leaves 147-152).
Abstracts in English and Chinese.
Acknowledgment --- p.i
Table of Contents --- p.ii
Abstract --- p.iii
Abstract (Chinese Version) --- p.iv
Abbreviation --- p.v
Chapter 1. --- Introduction --- p.1
Chapter 1.1 --- General Background --- p.1
Chapter 1.1.1 --- "1,3-Dipolar Cycloaddition" --- p.1
Chapter 1.1.2 --- Structure of Preparation of Nitrile Oxide --- p.3
Chapter 1.2 --- Intramolecular Nitrile Oxide Alkene Cyclization (INOC) --- p.7
Chapter 1.2.1 --- INOC in Organic Synthesis --- p.7
Chapter 1.2.2 --- Formation of Oximolactone as Unwanted Reaction in INOC --- p.10
Chapter 1.2.3 --- Nitrile Oxide Alkene Cyclization with Free Hydroxyl Group --- p.11
Chapter 1.3 --- Natural Occurring Gabosine --- p.14
Chapter 1.3.1 --- "Structure, Biological Effect and Syntheses of Gabosines" --- p.14
Chapter 1.3.2 --- Synthesis of Gabosine O and its 4-epimer --- p.17
Chapter 1.4 --- Protected 6-dehydroxy-Pseudo-a-D-Talose --- p.21
Chapter 1.4.1 --- Structures and Biological Effects of Valienamine and its Derivatives --- p.21
Chapter 1.4.2 --- Structural and Biological Studies of Valienamine by Our Group --- p.23
Chapter 2. --- Results and Discussion --- p.28
Chapter 2.1 --- Studies on INOC of Sugar Derivatives with Free Hydroxyl Group(s) --- p.28
Chapter 2.2 --- Enantiospecific Synthesis of 4-epi-Gabosine O --- p.47
Chapter 2.3 --- Enantiospecific Synthesis of Gabosine O --- p.84
Chapter 2.4 --- Synthesis of 6-Deoxy-Pseudo-a-D-Talose --- p.87
Chapter 3. --- Conclusion --- p.95
Chapter 4. --- Experimental --- p.100
References --- p.147
Appendix NMR spectra --- p.153
"Construction of carbocycles from carbohydrates via 1,3-dipolar cycloaddition". Thesis, 2011. http://library.cuhk.edu.hk/record=b6075206.
Pełny tekst źródłaBy using intramolecular nitrile oxide-alkene cycloaddition (INOC) as the kep step to construct hydroxylated carbocycles, gabosine F was synthesized for the first time from L-arabinose. Hence, theoretically, gabosine B, which is the enantiomer of gabosine F, can also be synthesized from D-arabinose by the same synthetic strategy.
In this thesis, the background information on the construction of carbocycles from carbohydrates via intramolecular 1,3-dipolar cycloaddition is presented. A review regarding the syntheses of gabosine B and cocaine are also descibed.
Starting with D-ribose, INAC of nitrones 113, 129, and 140, bearing an alpha/beta-unsaturated ester as the dipolarophile was studied. The INAC endo-cycloadduct 141 (cycloheptane) was converted into natural cocaine sucessfully, together with cocaine analogues 162,169,170,173,175, and 177.
The regioselectivity of intramolecular nitrone-alkene cycloaddition (INAC) was studied. The INAC of hept-6-enose nitrone 98, with a 3,4- trans-pentylidene acetal as the only blocking group, afforded endo-cycloadduct 97 (cycloheptane) exclusively. This result concluded that the regiospecific outcome of this INAC reaction is due to the present of the 3,4-trans-pentylidene acetal blocking group.
To investigate the regioselectivity in INAC of hex-5-enose with a 2,3- trans-pentylidene acetal blocking group, nitrones 178 and 195 were prepared from D-mannitol. endo-Cycloadducts (cyclohexanes) were afforded exclusively.
So, King Ho.
Adviser: Kung Ming Tony Shing.
Source: Dissertation Abstracts International, Volume: 73-06, Section: B, page: .
Thesis (Ph.D.)--Chinese University of Hong Kong, 2011.
Includes bibliographical references (leaves 165-171).
Electronic reproduction. Hong Kong : Chinese University of Hong Kong, [2012] System requirements: Adobe Acrobat Reader. Available via World Wide Web.
Electronic reproduction. [Ann Arbor, MI] : ProQuest Information and Learning, [201-] System requirements: Adobe Acrobat Reader. Available via World Wide Web.
Abstract also in Chinese.
Książki na temat "Carbocyclic ring compounds"
Carbocycle construction in terpene synthesis. New York, N.Y: VCH, 1988.
Znajdź pełny tekst źródłaCarbocyclic Three- and Four-membered Ring Compounds. G.Thieme Verlag,Germany, 1996.
Znajdź pełny tekst źródłaCarbocyclic Three- and Four-membered Ring Compounds. G.Thieme Verlag,Germany, 1997.
Znajdź pełny tekst źródłaMeijere, Armin De, (Ed.), red. Carbocyclic Three- and Four-membered Ring Compounds. G.Thieme Verlag,Germany, 1996.
Znajdź pełny tekst źródłaHouben-Weyl. Carbocyclic Three-and-four-membered Ring Compounds: Vols A-F (E17 Series). Thieme Publishing Group, 1997.
Znajdź pełny tekst źródłaSainsbury, Malcolm. Aromatic Compounds : Polybenzenoid Hydrocarbons and Their Derivatives : Hydrocarbon Ring Assemblies, Polyphenyl-Substituted Aliphatic Hydrocarbons and Their Derivatives , Monocarboxylic Acids of the Benzene Series: C7-C13-Carbocyclic Compoun. Elsevier, 2016.
Znajdź pełny tekst źródłaHo, Tse-Lok. Carbocycle Construction in Terpene Synthesis. Wiley & Sons, Incorporated, John, 1988.
Znajdź pełny tekst źródłaCzęści książek na temat "Carbocyclic ring compounds"
"3. By Ring Contraction". W Carbocyclic Three- and Four Membered Ring Compounds, redaktor Armin de Meijere. Stuttgart: Georg Thieme Verlag, 1997. http://dx.doi.org/10.1055/b-0035-112506.
Pełny tekst źródła"2. By Ring Contraction". W Carbocyclic Three- and Four Membered Ring Compounds, redaktor Armin de Meijere. Stuttgart: Georg Thieme Verlag, 1997. http://dx.doi.org/10.1055/b-0035-112522.
Pełny tekst źródła"2. With Ring Opening". W Carbocyclic Three- and Four Membered Ring Compounds, redaktor Armin de Meijere. Stuttgart: Georg Thieme Verlag, 1997. http://dx.doi.org/10.1055/b-0035-112548.
Pełny tekst źródła"2.1.1. Rearrangement of Homoallylic Compounds". W Carbocyclic Three- and Four-Membered Ring Compounds, redaktor Armin de Meijere. Stuttgart: Georg Thieme Verlag, 1997. http://dx.doi.org/10.1055/b-0035-113163.
Pełny tekst źródłaGrossel, Martin. "Introduction". W Alicyclic Chemistry. Oxford University Press, 1997. http://dx.doi.org/10.1093/hesc/9780198501046.003.0001.
Pełny tekst źródłaWard, Robert S. "Cyclisation versus polymerisation". W Bifunctional Compounds. Oxford University Press, 1994. http://dx.doi.org/10.1093/hesc/9780198558088.003.0011.
Pełny tekst źródła"3.5. From Cyclopropenes and Metal Carbonyl Compounds". W Carbocyclic Three- and Four-Membered Ring Compounds, redaktor Armin de Meijere. Stuttgart: Georg Thieme Verlag, 1997. http://dx.doi.org/10.1055/b-0035-112564.
Pełny tekst źródła"1. With Retention of the Ring". W Carbocyclic Three- and Four Membered Ring Compounds, redaktor Armin de Meijere. Stuttgart: Georg Thieme Verlag, 1997. http://dx.doi.org/10.1055/b-0035-112508.
Pełny tekst źródła"1. With Retention of the Ring". W Carbocyclic Three- and Four Membered Ring Compounds, redaktor Armin de Meijere. Stuttgart: Georg Thieme Verlag, 1997. http://dx.doi.org/10.1055/b-0035-112547.
Pełny tekst źródła"1. With Retention of the Ring". W Carbocyclic Three- and Four Membered Ring Compounds, redaktor Armin de Meijere. Stuttgart: Georg Thieme Verlag, 1997. http://dx.doi.org/10.1055/b-0035-112549.
Pełny tekst źródła