Academic literature on the topic '3-Sulfolene'

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Journal articles on the topic "3-Sulfolene"

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Subramanian, T., S. Meenakshi, Sumedha Y. Dange, and Sujata V. Bhat. "Facile Synthesis of 3-Aroyl-3-Sulfolenes Through Cycloadditions of Arylnitrile Oxides & 3-Sulfolene." Synthetic Communications 27, no. 15 (1997): 2557–62. http://dx.doi.org/10.1080/00397919708004123.

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Chou, Shang-Shing P., and Pi-Wei Liang. "Synthetic Applications of 3-(Phenylsulfinyl)-3-sulfolene." Journal of the Chinese Chemical Society 47, no. 1 (2000): 83–90. http://dx.doi.org/10.1002/jccs.200000009.

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SUBRAMANIAN, T., S. MEENAKSHI, S. Y. DANGE, and S. V. BHAT. "ChemInform Abstract: Facile Synthesis of 3-Aroyl-3-sulfolenes Through Cycloadditions of Arylnitrile Oxides and 3-Sulfolene." ChemInform 28, no. 42 (2010): no. http://dx.doi.org/10.1002/chin.199742150.

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Greenberg, Fred H. "Preparation of the bromohydrin of 3-sulfolene." Journal of Chemical Education 62, no. 7 (1985): 638. http://dx.doi.org/10.1021/ed062p638.

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Leonard, John, Andrew B. Hague, Martin F. Jones, and Richard A. Ward. "A Practical Large-Scale Synthesis of 3-Carbomethoxy-3-sulfolene." Synthesis 2000, no. 04 (2000): 507–9. http://dx.doi.org/10.1055/s-2000-6367.

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Chou, Shang-Shing P., and Chin-Chuan Sung. "Spirodialkylation of 3-(Phenylthio)-3-Sulfolene and Subsequent Synthetic Transformations." Journal of the Chinese Chemical Society 36, no. 6 (1989): 601–7. http://dx.doi.org/10.1002/jccs.198900079.

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Palchykov, Vitalii, Nina Khromykh, Yurii Lykholat, Svitlana Mykolenko, and Tetyana Lykholat. "Synthesis and Plant Growth Regulatory Activity of 3-Sulfolene Derivatives." Chemistry & Chemical Technology 13, no. 4 (2019): 424–28. http://dx.doi.org/10.23939/chcht13.04.424.

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Chou, Shang-Shing P., and Chien-Ming Lee. "Intramolecular Diels-Alder Reactions via 3-(Phenylthio)-4-(Trimethylsilyl)-3-Sulfolene." Journal of the Chinese Chemical Society 38, no. 5 (1991): 491–96. http://dx.doi.org/10.1002/jccs.199100082.

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Kishali, Nurhan, Yunus Kara, Ayse Tan, Birgul Koc, and Ertan Sahin. "Synthesis of New Cantharimide Analogues Derived from 3-Sulfolene." Synthesis 2011, no. 07 (2011): 1079–84. http://dx.doi.org/10.1055/s-0030-1258466.

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Desai, Shailesh R., Vinayak K. Gore, T. Mayelvaganan, R. Padmakumar, and Sujata V. Bhat. "Studies in alkylation of 3-methyl-3-sulfolene and thermolysis of resulting 2-alkyl-3-sulfolenes: Convenient synthesis of 1,2-disubstituted-1,3-dienes." Tetrahedron 48, no. 3 (1992): 481–90. http://dx.doi.org/10.1016/s0040-4020(01)89010-4.

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Dissertations / Theses on the topic "3-Sulfolene"

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Chaloner, Lynne Marie. "Heterocyclic o-quinodimethanes from 3-sulfolenes." Thesis, University of Liverpool, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.333628.

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Ardes-Guisot, Nicolas. "Intramolecular inverse demand diels-alder approaches to alkaloids starting from 3-carbomethoxy-3-sulfolenes." Thesis, University of Salford, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.491032.

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Over the last 4 years, our research interests were focused on the development of new methodologies for the synthesis of 5-substituted-3-carbomethoxy-3-sulfolenes, never reported before, and their application in total synthesis of natural products.
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ZHENG, MENG-YI, and 鄭孟琦. "New synthetic applications of 3-(phenylsulfonyl)-4-(trimethylsilyl)-3-sulfolene." Thesis, 1992. http://ndltd.ncl.edu.tw/handle/54393321674143814243.

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吳夢菊. "A Study of 3-Nitril-3-Sulfolene and Corresponding Derivatives." Thesis, 1992. http://ndltd.ncl.edu.tw/handle/45691830913648913618.

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LI, JUN-XIAN, and 李俊賢. "Intramolecular diels-alder reactions and applications via 3-(phenylsulfonyl)-3-sulfolene." Thesis, 1992. http://ndltd.ncl.edu.tw/handle/63658787292927238448.

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李明堅. "Intramolecular Dies-Alder Reaction of 3(Phenylthio)-4 -(trimethylsilyl)_3-Sulfolene." Thesis, 1990. http://ndltd.ncl.edu.tw/handle/45181212031021699364.

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碩士<br>輔仁大學<br>化學學系<br>78<br>3- (Phenylthio)-4-(trimethylsilyl)-3-sulfolene upon treatment with n-BuLi at low temperature reacted with 5-iodo-l-pentene or 6-iodo-l-hexene to give nucleophilic substitution reactions. Besides the expected C5 alkylation products, the C2 regioisomers were also obtained due to the competition of electron -withdrawing effect of the phenylthio group and the steric hindrance of the trimethylsilyl group. Heating the alkylation mixture in refluxing toluene effectively gave the diene resulting from desulfonylation of only the C5 alkylation products. Further heating of
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Brant, Michael Glenn. "Synthesis of Bicyclic Sulfones: Inhibitors of Neuraminidase." Thesis, 2015. http://hdl.handle.net/1828/6339.

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The lithiation of 3-sulfolene followed by subsequent treatment with an alkyl halide electrophile has been previously established as a method to produce 2-substituted-3-sulfolenes. Tandem reactivity with bis-alkyl halides has been observed to afford relatively simple bicyclic products. We hypothesized that it may be possible to access more complex bicyclic systems through use of bis-vinyl ketones as the electrophilic component. Herein, we present the outcome and mechanistic insights for the reaction between a variety of 3-sulfolene and substituted-3-sulfolene anions with bis-vinyl ketones to af
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Chang, Chin-Jyh, and 張欽智. "Reactions of 3-Sulfolenyl Zinc and 3-Sulfolenyl Copper with Electrophiles." Thesis, 1997. http://ndltd.ncl.edu.tw/handle/60885562331188234782.

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碩士<br>國立臺灣大學<br>化學系研究所<br>85<br>Sulfolenyl zinc can be prepared from sulfolenyl lithium by a metal ion exc hange reaction. This sulfolenyl zinc can react with carbonyl compounds to give addition products in high yields. Zinc sulfolenylate exhibits quite different regioselectivity from lithium sulfolenylate toward carbonyl carbonyl electro philes. Sulfolenyl copper, generated from sulfolenyl lithium and cuprous sal t, reacts with αβ-unsaturated ketones to produce 1,4-addition compounds. How ever, it r
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Pi-Wei, Liang, and 梁丕偉. "Synthesis and Applications of 3-Phenylsulfinyl-3-sulfolenes." Thesis, 2002. http://ndltd.ncl.edu.tw/handle/29986930596832262527.

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博士<br>輔仁大學<br>化學系<br>90<br>Abstract The 3-phenylsulfinyl-3-sulfolene 2 was readily prepared by m-CPBA oxidation of the sulfide 1. Thermal desulfonylation of 2 gave 2- phenylsulfinyl-1,3-butadiene 4. The Diels-Alder reactions of 4 with various dienophiles gave the cyclized products 5-15 in good yields. The regiochemistry was found to be dominated by the phenylsulfinyl group. Deprotonation of 2 by BuLi (1 equiv) followed by the reaction with alkyl halides gave the substituted 2-sulfolenes 16-20. A synthetic application of 20 was demonstrated by converting 20 to the bicyclic product 2
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LIU, SHI-YONG, and 劉勢勇. "Synthesis and applications of 3-phenylthio-3-sulfolenes." Thesis, 1987. http://ndltd.ncl.edu.tw/handle/63440232869806950856.

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Book chapters on the topic "3-Sulfolene"

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Koo, S. "Reaction with 3-Sulfolenes." In Monocyclic Arenes, Quasiarenes, and Annulenes. Georg Thieme Verlag KG, 2010. http://dx.doi.org/10.1055/sos-sd-045-01464.

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Leonard, John, Andrew B. Hague, and John A. Knight. "Chapter 6 Preparation of substituted 3-sulfolenes and their use as precursors for diels-alder dienes." In Synthetic and Stereochemical Aspects. Elsevier, 1998. http://dx.doi.org/10.1016/s1099-8268(98)80009-7.

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Conference papers on the topic "3-Sulfolene"

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Diyuk, Vitaliy E., Liudmyla M. Grishchenko, Galyna G. Tsapyuk, Anna V. Vakaliuk, Alexander N. Zaderko, and Vladyslav V. Lisnyak. "Functionalization of Multi-Walled Carbon Nanotubes with 3-Sulfolene and Diethyl Acetylenedicarboxylate." In 2020 IEEE 40th International Conference on Electronics and Nanotechnology (ELNANO). IEEE, 2020. http://dx.doi.org/10.1109/elnano50318.2020.9088811.

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