Relevant bibliographies by topics / Carbonyl halides

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  1. Journal articles

Academic literature on the topic 'Carbonyl halides'

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

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Journal articles on the topic "Carbonyl halides"

1

Vizer, S. A., and K. B. Yerzhanov. "Heterocycles Synthesis at Carbonylation of Acetylenic Compounds." Eurasian Chemico-Technological Journal 5, no. 2 (2016): 145. http://dx.doi.org/10.18321/ectj294.

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The carbonylation of unsaturated hydrocarbons, alcohols, organic halides and other substrates catalyzed by transition metals, salts of transition metals and organometallic complexes is a wide used synthesis method of new carbonyl, carboxyl and alkoxy carbonyl containing compounds including creation or modificationt of heterocycles. The data about synthesis of heterocycles at carbonylation of acetylenic compounds have been appeared at last 20 years and are demonstrated in our review. Introduction of carbon monoxide in the catalytic reactions of acetylenic compounds permits to obtain in oneput p
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2

Thomas, Nicholas C. "Substituted ruthenium carbonyl halides." Coordination Chemistry Reviews 70 (July 1986): 121–56. http://dx.doi.org/10.1016/0010-8545(86)80037-6.

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3

C. Thomas, N. "Substituted osmium carbonyl halides." Coordination Chemistry Reviews 93, no. 2 (1989): 225–44. http://dx.doi.org/10.1016/0010-8545(89)80017-7.

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4

Francisco, J. S., and Z. Li. "Dissociation pathways of carbonyl halides." Journal of Physical Chemistry 93, no. 24 (1989): 8118–22. http://dx.doi.org/10.1021/j100361a029.

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5

Zhang, Xu, Hong Yi, Zhixiong Liao, et al. "Copper-catalysed direct radical alkenylation of alkyl bromides." Org. Biomol. Chem. 12, no. 35 (2014): 6790–93. http://dx.doi.org/10.1039/c4ob00813h.

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A copper-catalysed direct radical alkenylation of benzyl bromides and α-carbonyl alkyl bromides has been developed. Compared with recent radical alkenylations which mostly focused on secondary or tertiary alkyl halides, this transformation shows good reactivity towards primary alkyl halides and tertiary/secondary alkyl halides are also tolerated.
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6

Nagaki, Aiichiro, Yuta Tsuchihashi, Suguru Haraki, and Jun-ichi Yoshida. "Benzyllithiums bearing aldehyde carbonyl groups. A flash chemistry approach." Organic & Biomolecular Chemistry 13, no. 26 (2015): 7140–45. http://dx.doi.org/10.1039/c5ob00958h.

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7

He, Ying, Qifa Liu, Xiaoyun Ma, and Ming Lu. "Oxidation of Benzyl Halides and Related Compounds to Carbonyl Compounds Using Hydrogen Peroxide Catalysed by Tempo in Water." Journal of Chemical Research 37, no. 1 (2013): 22–24. http://dx.doi.org/10.3184/174751912x13545558675784.

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A green and straightforward method for the oxidation of benzyl halides and some related compounds to the corresponding carbonyl compounds is reported using hydrogen peroxide catalysed by 2,2,6,6-tetramethyl-1-piperidinyloxy (TEMPO) in water. The corresponding carbonyl compounds were obtained with excellent yields in a short time.
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8

Du, Pan, Jiyang Zhao, Shanshan Liu, and Zhen Yue. "Insights into the nucleophilic substitution of pyridine at an unsaturated carbon center." RSC Advances 11, no. 39 (2021): 24238–46. http://dx.doi.org/10.1039/d1ra03019a.

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9

Zhu, Bolin, Xinwei Huang, and Xiaoting Hao. "Synthesis and structures of doubly-bridged dicyclopentadienyl dinuclear rhenium complexes, and their photochemical reactions with aromatic halides in benzene." Dalton Trans. 43, no. 44 (2014): 16726–36. http://dx.doi.org/10.1039/c4dt02370f.

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10

Liu, Xuan-Yu, Bu-Qing Cheng, Yi-Cong Guo, et al. "Iron-mediated highly diastereoselective allylation of carbonyl compounds with cyclic allylic halides." Organic Chemistry Frontiers 6, no. 10 (2019): 1581–86. http://dx.doi.org/10.1039/c9qo00210c.

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