Academic literature on the topic 'Aliphatic diazo compounds'

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Journal articles on the topic "Aliphatic diazo compounds"

1

Yates, Peter, and J. A. Eenkhorn. "Aliphatic diazo compounds." Tetrahedron 44, no. 11 (1988): 3159–70. http://dx.doi.org/10.1016/s0040-4020(01)85947-0.

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Pei, Guojing, Yuxia Liu, Guang Chen, Xiangai Yuan, Yuan-Ye Jiang, and Siwei Bi. "Unveiling the mechanisms and secrets of chemoselectivities in Au(i)-catalyzed diazo-based couplings with aryl unsaturated aliphatic alcohols." Catalysis Science & Technology 8, no. 17 (2018): 4450–62. http://dx.doi.org/10.1039/c8cy01352g.

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Griffiths, J. "Diazo Chemistry II: Aliphatic, inorganic and organometallic compounds." Dyes and Pigments 30, no. 3 (1996): 245–46. http://dx.doi.org/10.1016/0143-7208(96)90005-4.

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Bari, M. A., M. M. Karim, M. M. Hoque, and M. A. J. Miah. "Characterization and Synthesis of Some α, β-unsaturated Ester Derivatives from Aliphatic Aldehydes." Journal of Scientific Research 2, no. 2 (2010): 343–50. http://dx.doi.org/10.3329/jsr.v2i2.4167.

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Ethyl diazoacetate compound is useful synthetic intermediates for α, β-unsaturated ester in organic synthesis but, due to its toxicity and unpredictable explosive behaviour, its unique reactivity has not been fully exploited and the use on large scale has been avoided. We have developed a reliable method that generates EDA compound in situ. Our approach is based on the Wittig reaction, which utilizes EDA as diazo precursors. In the presence of Cu(OTf)2, we found that diazo compounds can be cleanly converted to alkenyl compounds under mild reaction conditions and in a narrow range of solvents.
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LADYZHNIKOVA, T. D., A. G. TYRKOV, K. V. ALTUKHOV, and G. A. BERKOVA. "ChemInform Abstract: Treatment of Cyanodinitroethoxycarbonylmethane with Aliphatic Diazo Compounds." ChemInform 25, no. 4 (2010): no. http://dx.doi.org/10.1002/chin.199404104.

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ZALESOV, V. V., S. S. KATAEV, E. V. PIMENOVA, and D. D. NEKRASOV. "ChemInform Abstract: Reaction of Oxygen-Containing 2,3-Dioxoheterocycles with Aliphatic Diazo Compounds." ChemInform 29, no. 32 (2010): no. http://dx.doi.org/10.1002/chin.199832053.

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Ziegler, Thomas. "Book Review: Diazo Chemistry II. Aliphatic, Inorganic and Organometallic Compounds. By H. Zollinger." Angewandte Chemie International Edition in English 35, no. 18 (1996): 2154. http://dx.doi.org/10.1002/anie.199621541.

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8

Mbuvi, Harun M., Erik R. Klobukowski, Gina M. Roberts, and L. Keith Woo. "O-H insertion and tandem N-H insertion/cyclization reactions using an iron porphyrin as catalyst with diazo compounds as carbene sources." Journal of Porphyrins and Phthalocyanines 14, no. 03 (2010): 284–92. http://dx.doi.org/10.1142/s1088424610001982.

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Iron(III) tetraphenylporphyrin chloride, Fe(TPP)Cl , efficiently catalyzed the insertion of carbenes derived from methyl 2-phenyldiazoacetates into O-H bonds of aliphatic and aromatic alcohols, with yields generally above 80%. Although the analogous N-H insertions are rapid at room temperature, the O-H insertion reactions are slower and required heating in refluxing methylene chloride for about 8 hours using 1.0 mol.% catalyst. Fe(TPP)Cl was also found to be effective for tandem N-H insertion/cyclization reactions when 1,2-diamines and 1,2-alcoholamines were treated with diazo reagents to give
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9

Steck, Viktoria, Gopeekrishnan Sreenilayam, and Rudi Fasan. "Selective Functionalization of Aliphatic Amines via Myoglobin-Catalyzed Carbene N–H Insertion." Synlett 31, no. 03 (2019): 224–29. http://dx.doi.org/10.1055/s-0039-1690007.

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Engineered myoglobins have recently gained attention for their ability to catalyze a variety of abiological carbene transfer reactions including the functionalization of amines via carbene insertion into N–H bonds. However, the scope of myoglobin and other hemoprotein-based biocatalysts in the context of this transformation has been largely limited to aniline derivatives as the amine substrates and ethyl diazoacetate as the carbene donor reagent. In this report, we describe the development of an engineered myoglobin-based catalyst that is useful for promoting carbene N–H insertion reactions ac
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10

Ivanov, A. V., G. Mlostoń, and V. A. Nikolaev. "Tetrasubstituted oxathioles and olefins obtained by cycloaddition of 2-diazo-1,3-dicarbonyl compounds to aliphatic thiones." Russian Journal of Organic Chemistry 49, no. 7 (2013): 1080–82. http://dx.doi.org/10.1134/s107042801307021x.

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Books on the topic "Aliphatic diazo compounds"

1

Zollinger, Heinrich. Diazo chemistry. VCH, 1995.

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2

Zollinger, Heinrich. Diazo chemistry.: Aromatic and heteroaromatic compounds. VCH, 1994.

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Zollinger, Heinrich. Diazo Chemistry II: Aliphatic, Inorganic and Organometallic Compounds. Wiley & Sons, Limited, John, 2004.

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Zollinger, Heinrich 1919. Azo and Diazo Chemistry: Aliphatic and Aromatic Compounds. Creative Media Partners, LLC, 2021.

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Zollinger, Heinrich. Diazo Chemistry II: Aliphatic, Inorganic and Organometallic Compounds. Wiley & Sons, Incorporated, John, 2020.

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Zollinger, Heinrich. Diazo Chemistry, Vol. 2, Aliphatic, Inorganic and Organometallic Compounds. Wiley-VCH, 1996.

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Book chapters on the topic "Aliphatic diazo compounds"

1

Maas, Gerhard. "Transition-metal catalyzed decomposition of aliphatic diazo compounds — New results and applications in organic synthesis." In Topics in Current Chemistry. Springer Berlin Heidelberg, 1987. http://dx.doi.org/10.1007/3-540-16904-0_15.

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REGITZ, MANFRED, and GERHARD MAAS. "Photochemistry of Aliphatic Diazo Compounds." In Diazo Compounds. Elsevier, 1986. http://dx.doi.org/10.1016/b978-0-12-585840-3.50008-8.

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REGITZ, MANFRED, and GERHARD MAAS. "Introduction to Syntheses of Aliphatic Diazo Compounds." In Diazo Compounds. Elsevier, 1986. http://dx.doi.org/10.1016/b978-0-12-585840-3.50009-x.

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Maas, Gerhard. "Transition-metal Catalyzed Decomposition of Aliphatic Diazo Compounds — New Results and Applications in Organic Synthesis." In Organic Synthesis, Reactions and Mechanisms. De Gruyter, 1987. http://dx.doi.org/10.1515/9783112597460-004.

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