Relevant bibliographies by topics / Lateral metalation

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Lateral metalation'

Author: Grafiati
Published: 4 June 2021
Last updated: 2 February 2022

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Journal articles on the topic "Lateral metalation"

1

Natale, Nicholas R., and Yousef R. Mirzaei. "THE LATERAL METALATION OF ISOXAZOLES. A REVIEW." Organic Preparations and Procedures International 25, no. 5 (1993): 515–56. http://dx.doi.org/10.1080/00304949309457997.

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NATALE, N. R., and Y. R. MIRZAEI. "ChemInform Abstract: The Lateral Metalation of Isoxazoles. A Review." ChemInform 26, no. 2 (2010): no. http://dx.doi.org/10.1002/chin.199502288.

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3

Miah, M. A. Jalil, Mukund P. Sibi, S. Chattopadhyay, Oluwole B. Familoni, and Victor Snieckus. "Directed ortho -Metalation of O -Aryl N ,N -Dialkylcarbamates: Methodology, Anionic ortho -Fries Rearrangement, and Lateral Metalation." European Journal of Organic Chemistry 2018, no. 4 (2017): 440–46. http://dx.doi.org/10.1002/ejoc.201701142.

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Mirzaei, Yousef R., Brenda Mallet Simpson, David J. Triggle, and Nicholas R. Natale. "Diastereoselectivity in the lateral metalation and electrophilic quenching of isoxazolyloxazolines." Journal of Organic Chemistry 57, no. 23 (1992): 6271–79. http://dx.doi.org/10.1021/jo00049a039.

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Boccuzzi, Tiziana, Luciana Cicco, Andrea Francesca Quivelli, et al. "2-Diphenylphosphinomethyl-3-methylpyrazine." Molbank 2021, no. 3 (2021): M1267. http://dx.doi.org/10.3390/m1267.

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The lateral metalation-electrophilic trapping reaction of alkyl-substituted pyrazines has always been challenging and poorly regioselective, with the corresponding derivatives often being isolated in moderate yield. In this contribution, we first report on the preparation of an unsymmetrically-substituted pyrazine, that is 2-diphenylphosphinomethyl-3-methylpyrazine, by subjecting to metalation with n-BuLi the commercially available 2,3-dimethylpyrazine, followed by interception of the putative lithiated benzyl-type intermediate with Ph2PCl. Such a functionalization has been successfully carrie
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6

R. Natale, Nicholas, and Chorng-Shyr Niou. "Synthesis, Metalation and Electrophilic Quenching of Alkyl-isoxazole-4-tertiary Carboxamides. A Critical Comparison of Three Isoxazole Lateral Metalation Methods." HETEROCYCLES 24, no. 2 (1986): 401. http://dx.doi.org/10.3987/r-1986-02-0401.

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7

MIRZAEI, Y. R., B. M. SIMPSON, D. J. TRIGGLE, and N. R. NATALE. "ChemInform Abstract: Diastereoselectivity in the Lateral Metalation and Electrophilic Quenching of Isoxazolyloxazolines." ChemInform 24, no. 10 (2010): no. http://dx.doi.org/10.1002/chin.199310209.

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8

Alessi, Manlio, Jignesh J. Patel, Kristina Zumbansen, and Victor Snieckus. "The Tetraethylphosphorodiamidate (OP(O)(NEt2)2) Directed Metalation Group (DMG). Directed ortho and Lateral Metalation and the Phospha Anionic Fries Rearrangement." Organic Letters 22, no. 6 (2020): 2147–51. http://dx.doi.org/10.1021/acs.orglett.0c00094.

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9

Focken, Thilo, Henning Hopf, Victor Snieckus, Ina Dix, and Peter G. Jones. "Stereoselective Lateral Functionalization of Monosubstituted [2.2]Paracyclophanes by Directedortho-Metalation−Homologous Anionic Fries Rearrangement." European Journal of Organic Chemistry 2001, no. 12 (2001): 2221–28. http://dx.doi.org/10.1002/1099-0690(200106)2001:12<2221::aid-ejoc2221>3.0.co;2-3.

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Miah, M. A. Jalil, Mukund P. Sibi, S. Chattopadhyay, Oluwole B. Familoni, and Victor Snieckus. "Front Cover: Directed ortho -Metalation of O -Aryl N ,N -Dialkylcarbamates: Methodology, Anionic ortho -Fries Rearrangement, and Lateral Metalation (Eur. J. Org. Chem. 4/2018)." European Journal of Organic Chemistry 2018, no. 4 (2018): 423. http://dx.doi.org/10.1002/ejoc.201800016.

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Dissertations / Theses on the topic "Lateral metalation"

1

Le, Tin Thanh. "Métallation et substitution nucléophile aromatique des acides benzoïques non protégés : application à la synthèse totale de l’apogossypol." Thesis, Le Mans, 2011. http://www.theses.fr/2011LEMA1016/document.

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Dans le cadre d’un projet général concernant l’étude de la réactivité des acidesbenzoïques non protégés avec les organométalliques, la synthèse totale d’analoguesstructuraux de l’apogossypol mettant en jeu des réactions de métallation aromatique a étéétudiée ainsi que la réaction de substitution nucléophile aromatique des acides benzoïquesortho-fluorés et ortho-méthoxylés.Le gossypol, (1,1’,6,6’,7,7’-hexahydroxy-5,5’-di-iso-propyl-3,3’-diméthyl-2,2’-binaphtalène-8,8’-dicarboxaldéhyde), pigment principal des graines du cotonnier, existe sousla forme de deux atropoisomères et possède de multiple
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