Relevant bibliographies by topics / Α-diazocarbonyl compounds

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters

Academic literature on the topic 'Α-diazocarbonyl compounds'

Author: Grafiati
Published: 6 September 2023

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Journal articles on the topic "Α-diazocarbonyl compounds"

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Krasavin, Mikhail, Maria Eremeyeva, Daniil Zhukovsky, and Dmitry Dar’in. "The Use of α-Diazo-γ-butyrolactams in the Büchner–Curtius–Schlotterbeck Reaction of Cyclic Ketones Opens New Entry to Spirocyclic Pyrrolidones." Synlett 31, no. 10 (March 23, 2020): 982–86. http://dx.doi.org/10.1055/s-0040-1708011.

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The only cyclic α-diazocarbonyl compound employed in the Büchner–Curtius–Schlotterbeck ring expansion of cyclic ketones to date was α-diazo-γ-butyrolactone. Encouraged by the recent success using α-diazo acetamides in related Tiffeneau–Demjanov type ring expansions, we extended this approach to various α-diazo-γ-butyrolactams, which produced, under BF3·OEt2-promoted conditions, spirocyclic seven-membered ketones. These findings substantially enhance the possibilities offered by cyclic α-diazocarbonyl compounds in constructing privileged spirocyclic scaffolds for drug design.
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Wang, Zikun, Xihe Bi, Yongjiu Liang, Peiqiu Liao, and Dewen Dong. "A copper-catalyzed formal O–H insertion reaction of α-diazo-1,3-dicarbonyl compounds to carboxylic acids with the assistance of isocyanide." Chem. Commun. 50, no. 30 (2014): 3976–78. http://dx.doi.org/10.1039/c4cc00402g.

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Straightforward synthetic access to α-acyloxy-1,3-dicarbonyl compounds is described via a novel Cu(ii)-catalyzed and isocyanide-assisted formal O–H insertion reaction of α-diazocarbonyl compounds to carboxylic acids.
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Dong, Shunxi, Xiaohua Liu, and Xiaoming Feng. "Asymmetric Catalytic Rearrangements with α-Diazocarbonyl Compounds." Accounts of Chemical Research 55, no. 3 (January 14, 2022): 415–28. http://dx.doi.org/10.1021/acs.accounts.1c00664.

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Ford, Alan, Hugues Miel, Aoife Ring, Catherine N. Slattery, Anita R. Maguire, and M. Anthony McKervey. "Modern Organic Synthesis with α-Diazocarbonyl Compounds." Chemical Reviews 115, no. 18 (August 18, 2015): 9981–10080. http://dx.doi.org/10.1021/acs.chemrev.5b00121.

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Lübcke, Marvin, Dina Bezhan, and Kálmán J. Szabó. "Trifluoromethylthiolation–arylation of diazocarbonyl compounds by modified Hooz multicomponent coupling." Chemical Science 10, no. 23 (2019): 5990–95. http://dx.doi.org/10.1039/c9sc00829b.

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Multicomponent reaction of diazocarbonyl and dibenzenesulfonimide-SCF3 reagents with BAr4 salts in the presence of Zn(NTf2)2 gives α,α′-difunctionalized trifluoromethylthio compounds.
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Chen, Xun, Ying Xie, Xinsheng Xiao, Guoqiang Li, Yuanfu Deng, Huanfeng Jiang, and Wei Zeng. "Rh(iii)-catalyzed chelation-assisted intermolecular carbenoid functionalization of α-imino Csp3–H bonds." Chemical Communications 51, no. 83 (2015): 15328–31. http://dx.doi.org/10.1039/c5cc06428g.

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Liu, Lu, and Junliang Zhang. "Gold-catalyzed transformations of α-diazocarbonyl compounds: selectivity and diversity." Chemical Society Reviews 45, no. 3 (2016): 506–16. http://dx.doi.org/10.1039/c5cs00821b.

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Gold-catalyzed diazo transformations display very unique reactivity and selectivity compared to other noble metals. This review will summarize gold-catalyzed transformations of α-diazocarbonyl compounds.
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Wang, Kang, Shufeng Chen, Hang Zhang, Shuai Xu, Fei Ye, Yan Zhang, and Jianbo Wang. "Pd(0)-catalyzed cross-coupling of allyl halides with α-diazocarbonyl compounds or N-mesylhydrazones: synthesis of 1,3-diene compounds." Organic & Biomolecular Chemistry 14, no. 15 (2016): 3809–20. http://dx.doi.org/10.1039/c6ob00454g.

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An efficient method for the synthesis of 1,3-butadiene derivatives based on Pd-catalyzed cross-coupling with allyl bromides or chlorides with α-diazocarbonyl compounds or N-mesylhydrazones is presented.
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Cortés González, Miguel A., Xingguo Jiang, Patrik Nordeman, Gunnar Antoni, and Kálmán J. Szabó. "Rhodium-mediated 18F-oxyfluorination of diazoketones using a fluorine-18-containing hypervalent iodine reagent." Chemical Communications 55, no. 89 (2019): 13358–61. http://dx.doi.org/10.1039/c9cc06905d.

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Ghorai, Jayanta, Manthena Chaitanya, and Pazhamalai Anbarasan. "Cp*Co(iii)-catalysed selective alkylation of C–H bonds of arenes and heteroarenes with α-diazocarbonyl compounds." Organic & Biomolecular Chemistry 16, no. 40 (2018): 7346–50. http://dx.doi.org/10.1039/c8ob02111b.

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Dissertations / Theses on the topic "Α-diazocarbonyl compounds"

1

Naganawa, Yuki. "Development of Novel Stereoselective Synthetic Methods Utilizing α-Diazocarbonyl Compounds in Acid Catalysis." 京都大学 (Kyoto University), 2011. http://hdl.handle.net/2433/142399.

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Book chapters on the topic "Α-diazocarbonyl compounds"

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Gilchrist, T. L. "From α-Diazocarbonyl Compounds." In Five-Membered Hetarenes with Three or More Heteroatoms, 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-013-00149.

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Sainsbury, M. "Synthesis from α-Diazocarbonyl Compounds." In X-Ene-X (X=F, Cl, Br, I, O, S, Se, Te, N, P), Ene-Hal, and Ene-O Compounds, 1. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-032-00231.

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Loh, T. P. "Reactions of α-Diazocarbonyl Compounds." In Compounds of Groups 13 and 2 (Al, Ga, In, Tl, Be...Ba), 1. Georg Thieme Verlag KG, 2004. http://dx.doi.org/10.1055/sos-sd-007-00355.

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Zaidlewicz, M., and M. Krzeminski. "Alkylation of α-Diazocarbonyl Compounds, and Other Diazo Compounds." In Boron Compounds, 1. Georg Thieme Verlag KG, 2005. http://dx.doi.org/10.1055/sos-sd-006-00953.

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Hou, X. L., X. S. Peng, K. S. Yeung, and H. N. C. Wong. "Rhodium-Catalyzed Reaction of α-Diazocarbonyl Compounds with Alkynes." In Fully Unsaturated Small-Ring Heterocycles and Monocyclic Five-Membered Hetarenes with One Heteroatom, 1. Georg Thieme Verlag KG, 2011. http://dx.doi.org/10.1055/sos-sd-109-00059.

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You might also be interested in the extended bibliographies on the topic 'Α-diazocarbonyl compounds' for particular source types:
Journal articles
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