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Journal articles on the topic 'Salts from aryl halides'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 February 2022

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1

Baik, Woonphil, Wanqiang Luan, Hyun Joo Lee, Cheol Hun Yoon, Sangho Koo, and Byeong Hyo Kim. "Efficient one-pot transformation of aminoarenes to haloarenes using halodimethylisulfonium halides generated in situ." Canadian Journal of Chemistry 83, no. 3 (March 1, 2005): 213–19. http://dx.doi.org/10.1139/v05-026.

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Halodimethylsulfonium halide 1, which is readily formed in situ from hydrohaloic acid and DMSO, is a good nucleophilic halide. This activated nucleophilic halide rapidly converts aryldiazonium salt prepared in situ by the same hydrohaloic acid and nitrite ion to aryl chlorides, bromides, or iodides in good yield. The combined action of nitrite ion and hydrohaloic acid in DMSO is required for the direct transformation of aromatic amines, which results in the production of aryl halides within 1 h. Substituted compounds with electron-donating or -withdrawing groups or sterically hindered aromatic amines are also smoothly transformed to the corresponding aromatic halides. The only observed by-product is the deaminated arene (usually <7%). The isolated aryldiazonium salts can also be converted to the corresponding aryl halides using 1. The present method offers a facile, one-step procedure for transforming aminoarenes to haloarenes and lacks the environmental pollutants that usually accompany the Sandmeyer reaction using copper halides. Key words: aminoarenes, haloarenes, halodimethylsulfonium halide, halogenation, amination.

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2

Zhang, Ying, Xiao Jiang, Jin-Mei Wang, Jing-Lei Chen, and Yong-Ming Zhu. "Palladium-catalyzed synthesis of aldehydes from aryl halides and tert-butyl isocyanide using formate salts as hydride donors." RSC Advances 5, no. 22 (2015): 17060–63. http://dx.doi.org/10.1039/c4ra16388e.

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3

Soleiman-Beigi, M., and Z. Arzehgar. "A Novel Method for the Direct Synthesis of Symmetrical and Unsymmetrical Sulfides and Disulfides from Aryl Halides and Ethyl Potassium Xanthogenate." Synlett 29, no. 07 (January 31, 2018): 986–92. http://dx.doi.org/10.1055/s-0037-1609081.

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An efficient and new method for the synthesis of disulfides and sulfides via the reaction of aryl halides with ethyl potassium xanthogenate in the presence of MOF-199 is described. O-Ethyl-S-aryl carbonodithioate has a key role as an intermediate in this procedure; it was converted into symmetrical diaryl disulfides in DMF. Additionally, this could be applied to the synthesis of unsymmetrical aryl alkyl(aryl′) disulfides by the reaction with S-alkyl(aryl) sulfurothioates (Bunte salts) as well as unsymmetrical aryl alkyl(aryl′) sulfides in DMSO.

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4

Yue, Huifeng, Chen Zhu, Li Shen, Qiuyang Geng, Katharina J. Hock, Tingting Yuan, Luigi Cavallo, and Magnus Rueping. "Nickel-catalyzed C–N bond activation: activated primary amines as alkylating reagents in reductive cross-coupling." Chemical Science 10, no. 16 (2019): 4430–35. http://dx.doi.org/10.1039/c9sc00783k.

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5

Micheletti, Gabriele, and Carla Boga. "Nucleophile/Electrophile Combinations in Aromatic Substitution: From Wheland to Wheland–Meisenheimer Intermediates Using Strongly Activated Arenes." Synthesis 49, no. 15 (July 13, 2017): 3347–56. http://dx.doi.org/10.1055/s-0036-1588490.

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This short review provides an overview on the interaction between 1,3,5-triaminobenzene derivatives and different kinds of electrophiles. Due to the ambident reactivity of these nucleophiles (i.e., at the nitrogen atom of the substituents and at the aromatic carbon atom) different compounds can be obtained. Particular attention is devoted to the detection, isolation, and characterization of covalent intermediates of aromatic substitution, starting from Wheland intermediates until the first detection and characterization of Wheland–Meisenheimer intermediates.1 Introduction2 Reactions between 1,3,5-Triaminobenzene Derivatives and Charged Electrophiles2.1 The Proton as an Electrophile2.2 Arenediazonium Salts as Electrophiles3 Reactions between 1,3,5-Triaminobenzene Derivatives and Neutral Electrophiles3.1 Alkyl Halides as Electrophiles3.2 Acyl Halides and Sulfonyl Chlorides as Electrophiles3.3 Aryl Halides and Heteroaryl Halides as Electrophiles3.4 Polynitroheteroaromatics as Electrophiles4 Conclusion

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6

Marcoux, David, and André B Charette. "Nickel-Catalyzed Synthesis of Phosphonium Salts from Aryl Halides and Triphenylphosphine." Advanced Synthesis & Catalysis 350, no. 18 (December 2008): 2967–74. http://dx.doi.org/10.1002/adsc.200800542.

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7

Zykova, A. "Synthesis and Structure of Aryl Phosphorus Compounds." Bulletin of the South Ural State University series "Chemistry" 12, no. 4 (2020): 5–50. http://dx.doi.org/10.14529/chem200401.

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Based on an analysis of the literature published from the late 20th century to the beginning of the 21st century, methods for the synthesis of some complex tetraorganylphosphonium salts are systematized and described, along with the features of the chemical transformations of pentaphenylphosphorus, which was first obtained in 1953. The tetraorganylphosphonium salts were known much earlier, however, the features of the synthesis of transition metal complexes, which are usually obtained from tetraorganylphosphorus halides and metal halides, have not been sufficiently studied. The present review is devoted to the discussion of these topics, since the famous Wittig Reaction is associated with aryl phosphorus compounds, which allows synthesizing alkenes of a given structure, and derivatives of transition metals rightfully occupy a special place among catalysts of various chemical processes. The continuation of these classical studies in the field of chemistry of organoelemental compounds takes place at one of the leading universities in Russia - South Ural State University in the laboratory of chemistry of organoelemental compounds at the Faculty of Chemistry. This article aims at familiarizing the reader with the achievements of Professor V.V. Sharutin and his students in the field of organophosphorus compounds. The main attention is paid to the reactions of pentaphenylphosphorus and its derivatives, as well as methods for the synthesis of ionic complexes of silver, gold, copper, titanium, zirconium, hafnium, ruthenium, osmium, cobalt, rhodium, iridium, palladium and platinum with tetraorganylphosphonium cations. The structural features of the described compounds and the possibility of using transition metal complexes in some catalytic reactions are described.

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8

Gooßen, Lukas J., Käthe Gooßen, Nuria Rodríguez, Mathieu Blanchot, Christophe Linder, and Bettina Zimmermann. "New catalytic transformations of carboxylic acids." Pure and Applied Chemistry 80, no. 8 (January 1, 2008): 1725–33. http://dx.doi.org/10.1351/pac200880081725.

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A series of metal-catalyzed processes are presented, in which carboxylic acids act as sources of either carbon nucleophiles or electrophiles, depending on the catalyst employed, the mode of activation, and the reaction conditions. A first reaction mode is the addition of carboxylic acids or amides over C-C multiple bonds, giving rise to enol esters or enamides, respectively. The challenge here is to control both the regio- and stereoselectivity of these reactions by the choice of the catalyst system. Alternatively, carboxylic acids can efficiently be decarboxylated using new Cu catalysts to give aryl-metal intermediates. Under protic conditions, these carbon nucleophiles give the corresponding arenes. If carboxylate salts are employed instead of the free acids, the aryl-metal species resulting from the catalytic decarboxylation can be utilized for the synthesis of biaryls in a novel cross-coupling reaction with aryl halides, thus replacing stoichiometric organometallic reagents. An activation with coupling reagents or simple conversion to esters allows the oxidative addition of carboxylic acids to transition-metal catalysts under formation of acyl-metal species, which can either be reduced to aldehydes, or coupled with nucleophiles. At elevated temperatures, such acyl-metal species decarbonylate, so that carboxylic acids become synthetic equivalents for aryl or alkyl halides, e.g., in Heck reactions.

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9

Henyecz, Réka, and György Keglevich. "New Developments on the Hirao Reactions, Especially from “Green” Point of View." Current Organic Synthesis 16, no. 4 (July 4, 2019): 523–45. http://dx.doi.org/10.2174/1570179416666190415110834.

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Background: The Hirao reaction discovered ca. 35 years ago is an important P–C coupling protocol between dialkyl phosphites and aryl halides in the presence of Pd(PPh3)4 as the catalyst and a base to provide aryl phosphonates. Then, the reaction was extended to other Preagents, such as secondary phosphine oxides and H-phosphinates and to other aryl and hetaryl derivatives to afford also phosphinic esters and tertiary phosphine oxides. Instead of the Pd(PPh3)4 catalyst, Pd(OAc)2 and Ni-salts were also applied as catalyst precursors together with a number of mono- and bidentate P-ligands. Objective: In our review, we undertook to summarize the target reaction with a special stress on the developments attained in the last 6 years, hence this paper is an update of our earlier reviews in a similar topic. Conclusion: “Greener” syntheses aimed at utilizing phase transfer catalytic and microwave-assisted approaches, even under “P-ligand-free. or even solvent-free conditions are the up-to date versions of the classical Hirao reaction. The mechanism of the reaction is also in the focus these days.

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10

Baskin, Jeremy M., and Zhaoyin Wang. "A mild, convenient synthesis of sulfinic acid salts and sulfonamides from alkyl and aryl halides." Tetrahedron Letters 43, no. 47 (November 2002): 8479–83. http://dx.doi.org/10.1016/s0040-4039(02)02073-7.

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11

Bellina, Fabio. "Real Metal-Free C–H Arylation of (Hetero)arenes: The Radical Way." Synthesis 53, no. 15 (March 15, 2021): 2517–44. http://dx.doi.org/10.1055/a-1437-9761.

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AbstractSynthetic methodologies involving the formation of carbon–carbon bonds from carbon–hydrogen bonds are of significant synthetic interest, both for efficiency in terms of atom economy and for their undeniable usefulness in late-stage functionalization approaches. Combining these aspects with being metal-free, the radical C–H intermolecular arylation procedures covered by this review represent both powerful and green methods for the synthesis of (hetero)biaryl systems.1 Introduction2 Arylation with Arenediazonium Salts and Related Derivatives2.1 Ascorbic Acid as the Reductant2.2 Hydrazines as Reductants2.3 Gallic Acid as the Reductant2.4. Polyanilines as Reductants2.5 Chlorpromazine Hydrochloride as the Reductant2.6 Phenalenyl-Based Radicals as Reductants2.7 Electrolytic Reduction of Diazonium Salts2.8 Visible-Light-Mediated Arylation3 Arylation with Arylhydrazines: Generation of Aryl Radicals Using an Oxidant4 Arylation with Diaryliodonium Salts5 Arylation with Aryl Halides6 Conclusions

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12

Ni, Shengyang, Chun-Xiao Li, Yu Mao, Jianlin Han, Yi Wang, Hong Yan, and Yi Pan. "Ni-catalyzed deaminative cross-electrophile coupling of Katritzky salts with halides via C─N bond activation." Science Advances 5, no. 6 (June 2019): eaaw9516. http://dx.doi.org/10.1126/sciadv.aaw9516.

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The reductive cross-coupling of sp3-hybridized carbon centers represents great synthetic values and insurmountable challenges. In this work, we report a nickel-catalyzed deaminative cross-electrophile coupling reaction to construct C(sp)─C(sp3), C(sp2)─C(sp3), and C(sp3)─C(sp3) bonds. A wide range of coupling partners including aryl iodides, bromoalkynes, or alkyl bromides are stitched with alkylpyridinium salts that derived from the corresponding primary amines. The advantages of this methodology are showcased in the two-step synthesis of the key lactonic moiety of (+)-compactin and (+)-mevinolin. The one-pot procedure without isolation of alkylpyridinium tetrafluoroborate salt is also proven to be successful. This cross-coupling strategy of two electrophiles provides a highly valuable vista for the convenient installation of alkyl substituents and late functionalizations of sp3 carbons.

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13

Ge, Xin, Fengli Sun, Xuemin Liu, Xinzhi Chen, Chao Qian, and Shaodong Zhou. "Mechanistic aspects of copper (II)-catalyzed synthesis of sulfones from sulfinate salts and aryl halides under C-S coupling." Molecular Catalysis 449 (April 2018): 72–78. http://dx.doi.org/10.1016/j.mcat.2017.12.016.

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14

Pal, Manojit. "Palladium-Catalyzed Alkynylation of Aryl and Hetaryl Halides: A Journey from Conventional Palladium Complexes or Salts to Palladium/Carbon." Synlett 2009, no. 18 (September 15, 2009): 2896–912. http://dx.doi.org/10.1055/s-0029-1218021.

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15

Zhang, Ying, Xiao Jiang, Jin-Mei Wang, Jing-Lei Chen, and Yong-Ming Zhu. "ChemInform Abstract: Palladium-Catalyzed Synthesis of Aldehydes from Aryl Halides and tert-Butyl Isocyanide Using Formate Salts as Hydride Donors." ChemInform 46, no. 28 (June 25, 2015): no. http://dx.doi.org/10.1002/chin.201528094.

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16

Rostami, Amin, Arash Ghaderi, Abed Rostami, Mohammad Gholinejad, and Sajedeh Gheisarzadeh. "Copper-Catalyzed C–S Bond Formation via the Cleavage of C–O Bonds in the Presence of S8 as the Sulfur Source." Synthesis 49, no. 22 (August 3, 2017): 5025–38. http://dx.doi.org/10.1055/s-0036-1588508.

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Useful and applicable methods for one-pot and odorless synthesis of unsymmetrical and symmetrical diaryl sulfides via C–O bond activation are presented. First, a new efficient procedure for the synthesis of unsymmetrical sulfides using the cross-coupling reaction of phenolic esters such as acetates, tosylates, and triflates and with arylboronic acid or triphenyltin chloride as the coupling partners is reported. Depending on the reaction, S8/KF or S8/NaOt-Bu system is found to be an effective source of sulfur in the presence of copper salts and in poly(ethylene glycol) as a green solvent. Then, the synthesis of symmetrical diaryl sulfides from phenolic compounds by using S8 as the sulfur source and NaOt-Bu in anhydrous DMF at 120 °C under N2 is described. By these protocols, the synthesis of a variety of unsymmetrical and symmetrical sulfides become easier than the available protocols in which thiols and aryl halides are directly used for the preparation of the sulfides.

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17

Ishida, H., and H. Nakajima. "Preparation of aryl alcohols from aryl halides." Zeolites 15, no. 4 (May 1995): 383. http://dx.doi.org/10.1016/0144-2449(95)99140-i.

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18

Brian, Ptoton Mnangat, and Peter Musau. "Synthesis, Reactivity and Stability of Aryl Halide Protecting Groups towards Di-Substituted Pyridines." Indonesian Journal of Chemistry 16, no. 1 (March 15, 2018): 53. http://dx.doi.org/10.22146/ijc.21177.

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This paper reports the synthesis and reactivity of different Benzyl derivative protecting groups. The synthesis and stability of Benzyl halides, 4-methoxybenzyl halides, 3,5-dimethoxybenzyl halides, 3,4-dimethoxybenzyl halides, 3,4,5-trimethoxybenzyl halide protecting groups and their reactivity towards nitrogen atom of a di-substituted pyridine ring in formation of pyridinium salts is also reported.

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19

Iyer, Suresh, Chinnasamy Ramesh, Anjana Sarkar, and Prakash P. Wadgaonkar. "The Vinylation of Aryl and Vinyl Halides Catalyzed by Copper Salts." Tetrahedron Letters 38, no. 46 (November 1997): 8113–16. http://dx.doi.org/10.1016/s0040-4039(97)10122-8.

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20

Pri-Bar, Ilan, and Ouri Buchman. "Hydroxycarbonylation of aryl halides with formate salts catalyzed by palladium complexes." Journal of Organic Chemistry 53, no. 3 (February 1988): 624–26. http://dx.doi.org/10.1021/jo00238a027.

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21

Quesnel, Jeffrey S., Alexander Fabrikant, and Bruce A. Arndtsen. "A flexible approach to Pd-catalyzed carbonylations via aroyl dimethylaminopyridinium salts." Chemical Science 7, no. 1 (2016): 295–300. http://dx.doi.org/10.1039/c5sc02949j.

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22

Fu, Zhengjiang, Guangguo Hao, Yaping Fu, Dongdong He, Xun Tuo, Shengmei Guo, and Hu Cai. "Transition metal-free electrocatalytic halodeborylation of arylboronic acids with metal halides MX (X = I, Br) to synthesize aryl halides." Organic Chemistry Frontiers 7, no. 3 (2020): 590–95. http://dx.doi.org/10.1039/c9qo01139k.

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23

Traficante, Carla I., Ernesto G. Mata, and Carina M. L. Delpiccolo. "Very efficient and broad-in-scope palladium-catalyzed Hiyama cross-coupling. The role of water and copper(i) salts." RSC Advances 5, no. 34 (2015): 26796–800. http://dx.doi.org/10.1039/c5ra03732h.

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24

Xu, Xin-Hua, and Wen-Qi Liu. "insertion of Selenium into Zinc Carbon Bonds and Its Application in the synthesis of Unsymmetrical Diarylselenides." Journal of Chemical Research 2002, no. 9 (September 2002): 444–45. http://dx.doi.org/10.3184/030823402103172590.

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Selenium inserts into the zinc carbon bond of aryl zinc halides to form the corresponding zinc selenoates; these react in THF-HMPA with diaryliodonium salts to afford unsymmetrical diaryl selenides in good yields.

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25

Allen, David W., Paul E. Cropper, and Ian W. Nowell. "The kinetic coordination template effect of an ortho(2,2′-bipyridyl) substituent in the metal ion-catalysed formation of arylphosphonium salts from an aryl halide. X-ray crystallographic confirmation and an unusual aspect of ligand reactivity in coordination compounds." Polyhedron 8, no. 8 (January 1989): 1039–43. http://dx.doi.org/10.1016/s0277-5387(00)81117-1.

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26

IYER, S., C. RAMESH, A. SARKAR, and P. P. WADGAONKAR. "ChemInform Abstract: The Vinylation of Aryl and Vinyl Halides Catalyzed by Copper Salts." ChemInform 29, no. 7 (June 24, 2010): no. http://dx.doi.org/10.1002/chin.199807092.

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27

LIU, Lei, Yao FU, and YuanYe JIANG. "Mechanism of palladium-catalyzed decarboxylative cross-coupling between cyanoacetate salts and aryl halides." SCIENTIA SINICA Chimica 42, no. 10 (September 1, 2012): 1493. http://dx.doi.org/10.1360/zb2012-42-10-1493.

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28

Jiang, YuanYe, Yao Fu, and Lei Liu. "Mechanism of palladium-catalyzed decarboxylative cross-coupling between cyanoacetate salts and aryl halides." Science China Chemistry 55, no. 10 (July 11, 2012): 2057–62. http://dx.doi.org/10.1007/s11426-012-4672-0.

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29

Beletskaya, Irina P., Alla G. Bessmertnykh, and Roger Guilard. "Palladium-catalyzed synthesis of aryl-substituted polyamine compounds from aryl halides." Tetrahedron Letters 38, no. 13 (March 1997): 2287–90. http://dx.doi.org/10.1016/s0040-4039(97)00363-8.

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30

Liang, Xifu, Jacob Andersen, Ulf Madsen, and Fredrik Björkling. "Rapid Synthesis of Aryl Azides from Aryl Halides under Mild Conditions." Synlett, no. 14 (2005): 2209–13. http://dx.doi.org/10.1055/s-2005-872248.

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31

Chen, Kai, Pei He, Shuai Zhang, and Pengfei Li. "Synthesis of aryl trimethylstannanes from aryl halides: an efficient photochemical method." Chemical Communications 52, no. 58 (2016): 9125–28. http://dx.doi.org/10.1039/c6cc01135g.

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An efficient transition-metal-free photochemical method featuring excellent functional group tolerance, mild reaction conditions and short reaction times has been discovered and developed for the synthesis of (hetero)aryl trimethylstannanes from (hetero)aryl halides.

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32

Chami, Zoubida, Monique Gareil, Jean Pinson, Jean Michel Saveant, and Andre Thiebault. "Aryl radicals from electrochemical reduction of aryl halides. Addition on olefins." Journal of Organic Chemistry 56, no. 2 (January 1991): 586–95. http://dx.doi.org/10.1021/jo00002a020.

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33

Shang, Rui, Dong-Sheng Ji, Ling Chu, Yao Fu, and Lei Liu. "Synthesis of α-Aryl Nitriles through Palladium-Catalyzed Decarboxylative Coupling of Cyanoacetate Salts with Aryl Halides and Triflates." Angewandte Chemie 123, no. 19 (April 6, 2011): 4562–66. http://dx.doi.org/10.1002/ange.201006763.

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34

Shang, Rui, Dong-Sheng Ji, Ling Chu, Yao Fu, and Lei Liu. "Synthesis of α-Aryl Nitriles through Palladium-Catalyzed Decarboxylative Coupling of Cyanoacetate Salts with Aryl Halides and Triflates." Angewandte Chemie International Edition 50, no. 19 (April 6, 2011): 4470–74. http://dx.doi.org/10.1002/anie.201006763.

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35

Zhu, Wei, and Dawei Ma. "Synthesis of Aryl Sulfones vial-Proline-Promoted CuI-Catalyzed Coupling Reaction of Aryl Halides with Sulfinic Acid Salts." Journal of Organic Chemistry 70, no. 7 (April 2005): 2696–700. http://dx.doi.org/10.1021/jo047758b.

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36

Roy, Amy H., and John F. Hartwig. "Reductive Elimination of Aryl Halides from Palladium(II)." Journal of the American Chemical Society 123, no. 6 (February 2001): 1232–33. http://dx.doi.org/10.1021/ja0034592.

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37

Porzelle, Achim, Michael D. Woodrow, and Nicholas C. O. Tomkinson. "Synthesis of Benzoxazolones from Nitroarenes or Aryl Halides." Organic Letters 12, no. 4 (February 19, 2010): 812–15. http://dx.doi.org/10.1021/ol902885j.

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38

Ren, Hongjun, Zhan Zhang, Lijun Xu, Zhengkai Chen, Zhubo Liu, Maozhong Miao, and Jinyu Song. "Nickel-Catalyzed Regioselective Reductive Cross-Coupling of Aryl Halides with Polysubstituted Allyl Halides in the Presence of Imidazolium Salts." Synlett 26, no. 20 (November 13, 2015): 2784–88. http://dx.doi.org/10.1055/s-0035-1560531.

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39

Lai, Chunqiu, and Bradley J. Backes. "Efficient preparation of S-aryl thioacetates from aryl halides and potassium thioacetate." Tetrahedron Letters 48, no. 17 (April 2007): 3033–37. http://dx.doi.org/10.1016/j.tetlet.2007.02.128.

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40

Hajipour, Abdol R., and Fatemeh Mohammadsaleh. "Synthesis of aryl azides from aryl halides promoted by Cu2O/tetraethylammonium prolinate." Tetrahedron Letters 55, no. 50 (December 2014): 6799–802. http://dx.doi.org/10.1016/j.tetlet.2014.10.045.

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41

Panda, Niranjan, Raghavender Mothkuri, and Dinesh Kumar Nayak. "Copper-Catalyzed Regioselective Synthesis ofN-Aryl Amides from Aldoximes and Aryl Halides." European Journal of Organic Chemistry 2014, no. 8 (February 7, 2014): 1602–5. http://dx.doi.org/10.1002/ejoc.201301868.

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42

Li, Yan, Huan-Huan Chen, Chu-Fei Wang, Xiao-Lan Xu, and Yi-Si Feng. "Ligand free palladium catalyzed decarboxylative cross-coupling of aryl halides with oxalate monoester salts." Tetrahedron Letters 53, no. 43 (October 2012): 5796–99. http://dx.doi.org/10.1016/j.tetlet.2012.08.076.

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43

Xu, Wei, Raju Mohan, and Michael M. Morrissey. "Polymer supported bases in combinatorial chemistry: Synthesis of aryl ethers from phenols and alkyl halides and aryl halides." Tetrahedron Letters 38, no. 42 (October 1997): 7337–40. http://dx.doi.org/10.1016/s0040-4039(97)01782-6.

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44

Tatunashvili, Elene, Bun Chan, Philippe E. Nashar, and Christopher S. P. McErlean. "σ-Bond initiated generation of aryl radicals from aryl diazonium salts." Organic & Biomolecular Chemistry 18, no. 9 (2020): 1812–19. http://dx.doi.org/10.1039/d0ob00205d.

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45

Hamada, Tatsuo, and Osamu Yonemitsu. "An Improved Synthesis of Arylsulfonyl Chlorides from Aryl Halides." Synthesis 1986, no. 10 (1986): 852–54. http://dx.doi.org/10.1055/s-1986-31803.

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46

Liu, Jianfei, Mei Qiu, and Xunjun Zhou. "Direct Synthesis of Some Oiaryl Ditellurides from Aryl Halides." Synthetic Communications 20, no. 18 (September 1990): 2759–67. http://dx.doi.org/10.1080/00397919008051487.

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47

Shi, Hang, Augustin Braun, Lu Wang, Steven H. Liang, Neil Vasdev, and Tobias Ritter. "Synthesis of 18 F-Difluoromethylarenes from Aryl (Pseudo) Halides." Angewandte Chemie 128, no. 36 (August 5, 2016): 10944–48. http://dx.doi.org/10.1002/ange.201604106.

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48

Saluste, C. Gustaf, Richard J Whitby, and Mark Furber. "A Palladium-Catalyzed Synthesis of Amidines from Aryl Halides." Angewandte Chemie 39, no. 22 (November 17, 2000): 4156–58. http://dx.doi.org/10.1002/1521-3773(20001117)39:22<4156::aid-anie4156>3.0.co;2-b.

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49

Shi, Hang, Augustin Braun, Lu Wang, Steven H. Liang, Neil Vasdev, and Tobias Ritter. "Synthesis of 18 F-Difluoromethylarenes from Aryl (Pseudo) Halides." Angewandte Chemie International Edition 55, no. 36 (August 5, 2016): 10786–90. http://dx.doi.org/10.1002/anie.201604106.

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