Relevant bibliographies by topics / Di-π-methane rearrangement

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  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Di-π-methane rearrangement'

Author: Grafiati
Published: 4 June 2021
Last updated: 11 February 2022

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Journal articles on the topic "Di-π-methane rearrangement"

1

Zimmerman, Howard E. "ChemInform Abstract: Di-π-Methane Rearrangement". ChemInform 43, № 39 (2012): no. http://dx.doi.org/10.1002/chin.201239272.

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Nair, Vijay, Gopinathan Anilkumar, Jaya Prabhakaran, Davis Maliakal, Guenter K. Eigendorf та Paul G. Williard. "Photochemical di-π-methane rearrangement of quinoxalinobarrelenes". Journal of Photochemistry and Photobiology A: Chemistry 111, № 1-3 (1997): 57–59. http://dx.doi.org/10.1016/s1010-6030(97)00256-6.

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ZIMMERMAN, H. E. "ChemInform Abstract: The Di-π-methane Rearrangement". ChemInform 23, № 38 (2010): no. http://dx.doi.org/10.1002/chin.199238310.

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Zimmerman, Howard E., та Diego Armesto. "Synthetic Aspects of the Di-π-methane Rearrangement". Chemical Reviews 96, № 8 (1996): 3065–112. http://dx.doi.org/10.1021/cr910109c.

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Rigo, Massimo, Manuela Weber, and Christian Müller. "Expanding the phosphorus–carbon analogy: formation of an unprecedented 5-phosphasemibullvalene derivative." Chemical Communications 52, no. 44 (2016): 7090–93. http://dx.doi.org/10.1039/c6cc02461k.

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ZIMMERMAN, H. E., та D. ARMESTO. "ChemInform Abstract: Synthetic Aspects of the Di-π-methane Rearrangement". ChemInform 28, № 14 (2010): no. http://dx.doi.org/10.1002/chin.199714325.

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Schlosser, Julika, Radek Cibulka, Philipp Groß, Heiko Ihmels та Christian J. Mohrschladt. "Visible‐Light‐Induced Di‐π‐Methane Rearrangement of Dibenzobarrelene Derivatives". ChemPhotoChem 4, № 2 (2019): 132–37. http://dx.doi.org/10.1002/cptc.201900221.

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Bender, Christopher Owen, Douglas Dolman, Jeremy Christian Foesier, Sherry Lee Lawson, and Kathryn Elvia Preuss. "The differing mechanisms of photo-formation of 7-cyanobenzocyclooctatetraene from 7- and 6-cyano-2,3-benzobicyclo[4.2.0]octa-2,4,7-triene." Canadian Journal of Chemistry 81, no. 1 (2003): 37–44. http://dx.doi.org/10.1139/v02-204.

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It is known that 7-cyanobenzocyclooctatetraene (COT 2) is a product of the thermolysis and direct photolysis of 7- and 6-cyano-2,3-benzobicyclo[4.2.0]octa-2,4,7-triene (1 and 5), though the mechanisms of these rearrangements have not been reported. In the present study experiments have been carried out using the deuterium-labelled trienes 1a (93%-d1 at C-6) and 5a (93%-d1 at C-8), which were formed from 2π + 2π photo-closure (direct irradiation) of COT 2a labelled at C-8. The results reveal that whereas the thermolysis of 1a and 5a and the direct irradiation of 5a reform COT 2a, probably via c
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Tanifuji, Naoki, Honghua Huang, Yoko Shinagawa та Keiji Kobayashi. "The di-π-methane rearrangement induced in tris(2-benzo[b]thienyl)methane". Tetrahedron Letters 44, № 4 (2003): 751–54. http://dx.doi.org/10.1016/s0040-4039(02)02713-2.

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Ihmels, Heiko, та Jia Luo. "Synthesis of cationic dibenzosemibullvalene-based phase-transfer catalysts by di-π-methane rearrangements of pyrrolinium-annelated dibenzobarrelene derivatives". Beilstein Journal of Organic Chemistry 7 (26 січня 2011): 119–26. http://dx.doi.org/10.3762/bjoc.7.17.

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Dibenzobarrelene derivatives, that are annelated with a pyrrolinium unit [N,N-dialkyl-3,4-(9',10'-dihydro-9',10'-anthraceno-3-pyrrolinium) derivatives], undergo a photo-induced di-π-methane rearrangement upon triplet sensitization to give the corresponding cationic dibenzosemibullvalene derivatives [N,N-dialkyl-3,4-{8c,8e-(4b,8b-dihydrodibenzo[a,f]cyclopropa[cd]pentaleno)}pyrrolidinium derivatives]. Whereas the covalent attachment of a benzophenone functionality to the pyrrolinium nitrogen atom did not result in an internal triplet sensitization, the introduction of a benzophenone unit as part
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Dissertations / Theses on the topic "Di-π-methane rearrangement"

1

Derstine, Brenden Paul. "PHOTOCHEMICAL AND TITANIUM (II) MEDIATED METHODS FOR THE SYNTHESIS OF COMPLEX MOLECULAR SCAFFOLDS." Diss., Temple University Libraries, 2018. http://cdm16002.contentdm.oclc.org/cdm/ref/collection/p245801coll10/id/497266.

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Chemistry<br>Ph.D.<br>Development of therapeutics is an extensive process, consuming significant amounts of time and requiring herculean synthetic efforts. A new therapeutic is most often designed from a previously commercialized scaffold, to increase the chance of success. Designing new molecular scaffolds can be extremely high risk and time consuming, yet at the same time the reward can be substantial. Accessing new molecular scaffolds, with efficient and “green” methods, is important in modern medicinal chemistry to diversify chemical space for therapeutic targets. There may be significant
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Book chapters on the topic "Di-π-methane rearrangement"

1

Li, Jie Jack. "Di-π-methane rearrangement." In Name Reactions. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/978-3-662-04835-1_84.

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Li, Jie Jack. "Di–π–methane rearrangement." In Name Reactions. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-01053-8_82.

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Li, Jie Jack. "Di-π-methane rearrangement." In Name Reactions. Springer Berlin Heidelberg, 2003. http://dx.doi.org/10.1007/978-3-662-05336-2_89.

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4

Banwell, Martin G., and David J. Y. D. Bon. "Applications of Di-Π-Methane and Related Rearrangement Reactions in Chemical Synthesis." In Molecular Rearrangements in Organic Synthesis. John Wiley & Sons, Inc, 2015. http://dx.doi.org/10.1002/9781118939901.ch9.

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Zimmerman, Howard. "Di-π-Methane Rearrangement." In CRC Handbook of Organic Photochemistry and Photobiology, Third Edition - Two Volume Set. CRC Press, 2012. http://dx.doi.org/10.1201/b12252-22.

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"36. Di‒π‒Methane Rearrangement." In Organic Chemistry: 100 Must-Know Mechanisms. De Gruyter, 2020. http://dx.doi.org/10.1515/9783110608373-036.

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Zimmerman, Howard E. "The Di-π-methane Rearrangement." In Organic Photochemistry. Routledge, 2017. http://dx.doi.org/10.1201/9780203744826-1.

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Rao, V., and Kolupula Srinivas. "Oxa-Di-π-Methane Rearrangement of _,_-Unsaturated Ketones." In CRC Handbook of Organic Photochemistry and Photobiology, Third Edition - Two Volume Set. CRC Press, 2012. http://dx.doi.org/10.1201/b12252-23.

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You might also be interested in the extended bibliographies on the topic 'Di-π-methane rearrangement' for particular source types:
Journal articles
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