Relevant bibliographies by topics / Substituted diaryl diselenides

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Substituted diaryl diselenides'

Author: Grafiati
Published: 4 June 2021
Last updated: 7 February 2022

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Journal articles on the topic "Substituted diaryl diselenides"

1

Nedel, Fernanda, Vinicius F. Campos, Diego Alves, et al. "Substituted diaryl diselenides: Cytotoxic and apoptotic effect in human colon adenocarcinoma cells." Life Sciences 91, no. 9-10 (2012): 345–52. http://dx.doi.org/10.1016/j.lfs.2012.07.023.

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2

Bhabak, Krishna P., and Debasish Bhowmick. "Synthetic strategies of gold(I)-selenolates from ortho-substituted diaryl diselenides via selenol and selenenyl sulfide intermediates." Inorganica Chimica Acta 450 (August 2016): 337–45. http://dx.doi.org/10.1016/j.ica.2016.06.022.

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3

Yu, Lei, Bo Chen, and Xian Huang. "Multicomponent reactions of allenes, diaryl diselenides, and nucleophiles in the presence of iodosobenzene diacetate: direct synthesis of 3-functionalized-2-arylselenyl substituted allyl derivatives." Tetrahedron Letters 48, no. 6 (2007): 925–27. http://dx.doi.org/10.1016/j.tetlet.2006.12.026.

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4

Wang, Jin-Xian, Xiaowei Wu, Yulai Hu, Kai Zhao, and Zhanxiang Liu. "Synthesis of Substituted Glycerol Selenide Ethers under Microwave Irradiation." Journal of Chemical Research 23, no. 12 (1999): 688–89. http://dx.doi.org/10.1177/174751989902301202.

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Substituted glycerol selenide ethers are rapidly obtained in high yields and good regioselectivities by reducing dialkyl diselenides with sodium tetrahydroborate in a basic environment followed by reaction with glycidyl sulfide ether under microwave irradiation conditions.
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5

Heredia, Adrián A., and Alicia B. Peñéñory. "Transition-metal-free one-pot synthesis of alkynyl selenides from terminal alkynes under aerobic and sustainable conditions." Beilstein Journal of Organic Chemistry 13 (May 16, 2017): 910–18. http://dx.doi.org/10.3762/bjoc.13.92.

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Alkynyl selenides were synthesized by a straightforward one-pot and three-step methodology, without the need of diselenides as starting reagents, under an oxygen atmosphere and using PEG 200 as the solvent. This procedure involves the in situ generation of dialkyl diselenides through a K3PO4-assisted reaction of an alkyl selenocyanate obtained by a nucleophilic substitution reaction between KSeCN and alkyl halides. Successive reaction with terminal alkynes in the presence of t-BuOK affords the corresponding alkyl alkynyl selenide in moderate to good yields. Finally, this methodology allowed th
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Murata, Yuki, Naoaki Otake, Moeko Sano, Mio Matsumura, and Shuji Yasuike. "Copper‐catalyzed C‐H selenations of 2‐substituted benzo[b]furans with diaryl diselenides: Synthesis of 2‐substituted 3‐selanylbenzo[b]furan derivatives." Asian Journal of Organic Chemistry, September 15, 2021. http://dx.doi.org/10.1002/ajoc.202100527.

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7

Yu, Lei, Bo Chen, and Xian Huang. "Multicomponent Reactions of Allenes, Diaryl Diselenides, and Nucleophiles in the Presence of Iodosobenzene Diacetate: Direct Synthesis of 3-Functionalized-2-arylselenyl Substituted Allyl Derivatives." ChemInform 38, no. 20 (2007). http://dx.doi.org/10.1002/chin.200720171.

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Dissertations / Theses on the topic "Substituted diaryl diselenides"

1

Nedel, Fernanda. "Seleção de novas moléculas e modalidades de tratamento no combate ao câncer." Universidade Federal de Pelotas, 2012. http://repositorio.ufpel.edu.br/handle/ri/1209.

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Made available in DSpace on 2014-08-20T13:32:46Z (GMT). No. of bitstreams: 1 tese_fernanda_nedel.pdf: 5232153 bytes, checksum: 94c9f4584571a1e142e44a8b165fc8dd (MD5) Previous issue date: 2012-09-17<br>Cancer is a leading cause of death and its rates are expected to increase 50% by 2020. Although surgical resection and additional therapies (such as chemotherapy and radiotherapy) are able to cure well-confined, primary tumors, the same does not apply during metastasis due to the systemic involvement and its resistance to conventional therapies. Therefore, the current clinical challenge is to
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