Relevant bibliographies by topics / Photochemistry. Cyclopropane

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Photochemistry. Cyclopropane'

Author: Grafiati
Published: 4 June 2021
Last updated: 13 February 2022

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Journal articles on the topic "Photochemistry. Cyclopropane"

1

ZIMMERMAN, H. E. "ChemInform Abstract: Cyclopropane Photochemistry." ChemInform 28, no. 8 (2010): no. http://dx.doi.org/10.1002/chin.199708307.

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2

Engel, Paul S., and Wen Xue Wu. "Photochemistry of [(trifluoromethyl)azo]cyclopropane: a reinvestigation." Journal of Organic Chemistry 55, no. 5 (1990): 1503–5. http://dx.doi.org/10.1021/jo00292a024.

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3

Carson, Philip A., and Paul de Mayo. "Surface photochemistry: Semiconductor mediated reactions of some 1,2-diarylcyclopropanes." Canadian Journal of Chemistry 65, no. 5 (1987): 976–79. http://dx.doi.org/10.1139/v87-166.

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1,2-Diphenylcyclopropane (1) was found to be oxidized on illuminated ZnO in the presence of air while 1-(p-methoxyphenyl)-2-phenylcyclopropane (2) and 1,2-bis(p-methoxyphenyl)cyclopropane (3) were found to be similarly oxidized on illuminated CdS. Compounds 2 and 3 were found, also, to undergo a rapid photochemical cis-trans isomerization on CdS whereas 1 did not undergo such isomerization. An electron transfer mechanism involving formation of the radical cations of the substrates is proposed.
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4

Altundas, Ramazan, and Metin Balci. "The Di-p-methane Photorearrangement of 2,3-Disubstituted Benzobarrelenes: the Effect of Substituents of Opposite Polarity on the Regioselectivity." Australian Journal of Chemistry 50, no. 8 (1997): 787. http://dx.doi.org/10.1071/c97047.

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The solution phase photochemistry of benzobarrelene derivatives (8) and (11), containing electron-donating and electron-withdrawing substituents, has been studied. The structures of the photoproducts (16)/(20) and (17)/(21) indicate clearly that vinyl-vinyl nitrile (aldehyde) bridging is not operating. The formation of these products is discussed in terms of the stabilizing effect of the substituents on the radical and the destabilizing effect on the formation of the cyclopropane ring.
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5

KATAGI, Toshiyuki, Yasuo KIKUZONO, Nobuyoshi MIKAMI, Tadashi MATSUDA, and Junshi MIYAMOTO. "A Theoretical Approach to Photochemistry of Pyrethroids Possessing the Cyclopropane Ring." Journal of Pesticide Science 13, no. 1 (1988): 129–32. http://dx.doi.org/10.1584/jpestics.13.129.

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6

Herbertz, Torsten, and Heinz D. Roth. "Electron Transfer Photochemistry of Homochrysanthemol: Intramolecular Nucleophilic Attack on the Cyclopropane Ring." Journal of Organic Chemistry 64, no. 10 (1999): 3708–13. http://dx.doi.org/10.1021/jo9903048.

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7

FANG, WEI-HAI, та DAVID LEE PHILLIPS. "PHOTOCHEMISTRY OF BUTYROPHENONE AND ITS α-SUBSTITUTED DERIVATIVE: A THEORETICAL EXAMINATION OF A NEW PHOTOCHEMICAL ROUTE TO CYCLOPROPANE GROUP FORMATION". Journal of Theoretical and Computational Chemistry 02, № 01 (2003): 23–31. http://dx.doi.org/10.1142/s0219633603000355.

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The potential energy surfaces of dissociations and isomerizations for butyrophenone and its α-substituted derivative in low-lying electronic states have been studied with use of the CASSCF and DFT methods. A three-surface (S1, T1 and T2) intersection was found in the present work and this plays an important role in the S1 → T1 process for butyrophenone and related aromatic carbonyl compounds. Examination of these results provides some new insights into the mechanistic photochemistry of aromatic ketones. The most probable mechanism leading to formation of a cyclopropane moiety was obtained on t
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8

Kline, Ellen S., Robert H. Hauge, Zakya H. Kafafi, and John L. Margrave. "Nickel and cyclopropane reactions and photochemistry using matrix-isolation Fourier-transform IR spectroscopy. Nickelacyclobutane synthesis and photofragmentation." Organometallics 7, no. 7 (1988): 1512–16. http://dx.doi.org/10.1021/om00097a010.

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9

Demuth, Martin, Bernhard Wietfeld, Bipin Pandey, and Kurt Schaffner. "Photochemistry of 1-Methoxybicyclo[2.2.2] octenones; Photolytic Cyclopropane Cleavage of the Initially Formed Tricyclo [3.3.0.02,8]octan-3-ones." Angewandte Chemie International Edition in English 24, no. 9 (1985): 763–64. http://dx.doi.org/10.1002/anie.198507631.

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10

Bischofberger, Norbert, Bruno Frei, and Oskar Jeger. "Photochemical reactions. 146th communication. Photochemistry of conjugated methano-epoxydienes: Participation of the neighboring cyclopropane ring in product formationvia carbonyl ylide and carbene intermediates." Helvetica Chimica Acta 68, no. 6 (1985): 1583–91. http://dx.doi.org/10.1002/hlca.19850680610.

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Dissertations / Theses on the topic "Photochemistry. Cyclopropane"

1

Kan, Tze-wai Jovi. "Development of new polymer-supported reagents for organic synthesis, solvent effects in samarium promoted allylic alcohol cyclopropanation reactions and time resolved resonance studies of the photodeprotection of p-hydroxyphenacyl caged phototrigger compounds." Click to view the E-thesis via HKUTO, 2006. http://sunzi.lib.hku.hk/hkuto/record/B37925660.

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Kan, Tze-wai Jovi, and 簡紫慧. "Development of new polymer-supported reagents for organic synthesis, solvent effects in samarium promoted allylic alcohol cyclopropanationreactions and time resolved resonance studies of the photodeprotectionof p-hydroxyphenacyl caged phototrigger compounds." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2006. http://hub.hku.hk/bib/B37925660.

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