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Relevant bibliographies by topics / Carbon-heteroatom Bond Forming Reactions

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Academic literature on the topic 'Carbon-heteroatom Bond Forming Reactions'

Author: Grafiati

Published: 6 September 2023

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Journal articles on the topic "Carbon-heteroatom Bond Forming Reactions"

1

Corma, A., A. Leyva-Pérez, and Maria J. Sabater. "Gold-Catalyzed Carbon−Heteroatom Bond-Forming Reactions." Chemical Reviews 111, no. 3 (2011): 1657–712. http://dx.doi.org/10.1021/cr100414u.

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2

Lumb, Jean-Philip, and Kenneth Esguerra. "Cu(III)-Mediated Aerobic Oxidations." Synthesis 51, no. 02 (2018): 334–58. http://dx.doi.org/10.1055/s-0037-1609635.

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CuIII species have been invoked in many copper-catalyzed transformations including cross-coupling reactions and oxidation reactions. In this review, we will discuss seminal discoveries that have advanced our understanding of the CuI/CuIII redox cycle in the context of C–C and C–heteroatom aerobic cross-coupling reactions, as well as C–H oxidation reactions mediated by CuIII–dioxygen adducts.1 General Introduction2 Early Examples of CuIII Complexes3 Aerobic CuIII-Mediated Carbon–Heteroatom Bond-Forming Reactions4 Aerobic CuIII-Mediated Carbon–Carbon Bond-Forming Reactions5 Bioinorganic Studies

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3

Takemoto, Yoshiji, and Hideto Miyabe. "ChemInform Abstract: Asymmetric Carbon-Heteroatom Bond-Forming Reactions." ChemInform 42, no. 18 (2011): no. http://dx.doi.org/10.1002/chin.201118241.

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4

Daoust, Benoit, Nicolas Gilbert, Paméla Casault, François Ladouceur, and Simon Ricard. "1,2-Dihaloalkenes in Metal-Catalyzed Reactions." Synthesis 50, no. 16 (2018): 3087–113. http://dx.doi.org/10.1055/s-0037-1610174.

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1,2-Dihaloalkenes readily undergo simultaneous or sequential difunctionalization through transition-metal-catalyzed reactions, which makes them attractive building blocks for complex unsaturated motifs. This review summarizes recent applications of such transformations in C–C and C–heteroatom bond forming processes. The facile synthesis of stereodefined alkene derivatives, as well as aromatic and heteroatomic compounds, from 1,2-dihaloalkenes is thus outlined.1 Introduction2 Synthesis of 1,2-Dihaloalkenes3 C–C Bond Forming Reactions4 C–Heteroatom Bond Forming Reactions5 Conclusion

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5

Miyabe, Hideto, and Yoshiji Takemoto. "Cascade radical reactions via carbon-carbon/heteroatom bond-forming process." Universal Organic Chemistry 2, no. 1 (2014): 1. http://dx.doi.org/10.7243/2053-7670-2-1.

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6

Hosoya, Keisuke, Minami Odagi, and Kazuo Nagasawa. "Guanidine organocatalysis for enantioselective carbon-heteroatom bond-forming reactions." Tetrahedron Letters 59, no. 8 (2018): 687–96. http://dx.doi.org/10.1016/j.tetlet.2017.12.058.

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7

Corma, A., A. Leyva-Perez, and Maria J. Sabater. "ChemInform Abstract: Gold-Catalyzed Carbon-Heteroatom Bond-Forming Reactions." ChemInform 42, no. 29 (2011): no. http://dx.doi.org/10.1002/chin.201129225.

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8

Banerjee, Bubun. "Microwave-assisted Carbon-carbon and Carbon-heteroatom Bond Forming Reactions - Part 1A." Current Microwave Chemistry 7, no. 1 (2020): 3–4. http://dx.doi.org/10.2174/221333560701200422091717.

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9

Banerjee, Bubun. "Microwave-assisted Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions - Part 1B." Current Microwave Chemistry 7, no. 2 (2020): 84–85. http://dx.doi.org/10.2174/221333560702200714141435.

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10

Banerjee, Bubun. "Microwave-assisted Carbon-Carbon and Carbon-Heteroatom Bond Forming Reactions - Part 2A." Current Microwave Chemistry 8, no. 2 (2021): 56–57. http://dx.doi.org/10.2174/221333560802211028163413.

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