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Relevant bibliographies by topics / Heck-type reaction

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Academic literature on the topic 'Heck-type reaction'

Author: Grafiati

Published: 6 September 2023

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Journal articles on the topic "Heck-type reaction"

1

Kurandina, Daria, Padon Chuentragool, and Vladimir Gevorgyan. "Transition-Metal-Catalyzed Alkyl Heck-Type Reactions." Synthesis 51, no. 05 (February 7, 2019): 985–1005. http://dx.doi.org/10.1055/s-0037-1611659.

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The Heck reaction is one of the most reliable and useful strategies for the construction of C–C bonds in organic synthesis. However, in contrast to the well-established aryl Heck reaction, the analogous reaction employing alkyl electrophiles is much less developed. Significant progress in this area was recently achieved by merging radical-mediated and transition-metal-catalyzed approaches. This review summarizes the advances in alkyl Heck-type reactions from its discovery early in the 1970s up until the end of 2018.1 Introduction2 Pd-Catalyzed Heck-Type Reactions2.1 Benzylic Electrophiles2.2 α-Carbonyl Alkyl Halides2.3 Fluoroalkyl Halides2.4 α-Functionalized Alkyl Halides2.5 Unactivated Alkyl Electrophiles3 Ni-Catalyzed Heck-Type Reactions3.1 Benzylic Electrophiles3.2 α-Carbonyl Alkyl Halides3.3 Unactivated Alkyl Halides4 Co-Catalyzed Heck-Type Reactions5 Cu-Catalyzed Heck-Type Reactions6 Other Metals in Heck-Type Reactions7 Conclusion

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Zhou, Huan, Liang Ge, Jinshuai Song, Wujun Jian, Yajun Li, Chunsen Li, and Hongli Bao. "HOTf-Catalyzed Alkyl-Heck-type Reaction." iScience 3 (May 2018): 255–63. http://dx.doi.org/10.1016/j.isci.2018.04.020.

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Lee, A. L. "Enantioselective oxidative boron Heck reactions." Organic & Biomolecular Chemistry 14, no. 24 (2016): 5357–66. http://dx.doi.org/10.1039/c5ob01984b.

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Wang, Sa-Sa, and Guo-Yu Yang. "Recent developments in low-cost TM-catalyzed Heck-type reactions (TM = transition metal, Ni, Co, Cu, and Fe)." Catalysis Science & Technology 6, no. 9 (2016): 2862–76. http://dx.doi.org/10.1039/c5cy02235e.

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Newman, Stephen, and Jaya Vandavasi. "A High-Throughput Approach to Discovery: Heck-Type Reactivity with Aldehydes." Synlett 29, no. 16 (June 12, 2018): 2081–86. http://dx.doi.org/10.1055/s-0037-1610161.

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The classical Heck reaction is among the most powerful methods available for the construction of C–C bonds. Modification of this transformation to utilize diverse organohalide coupling partners has resulted in new reactions such as the silyl-Heck, aza-Heck, and boryl-Heck reactions. In contrast, modification of the olefin coupling partner is rare. For instance, use of the π-bond of an aldehyde instead of an alkene would provide ketones via a carbonyl-Heck process. This seemingly minor manipulation of the Heck reaction has proven surprisingly difficult to realize in practice. Through the use of high-throughput experimentation techniques, an efficient catalyst system for this transformation was identified, enabling the intermolecular coupling of organotriflates and aldehydes to synthesize diverse ketones.

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Zhu, Xiaoyan, Feng Liu, Xinwu Ba, and Yonggang Wu. "Tandem Suzuki Polymerization/Heck Cyclization Reaction to Form Ladder-Type 9,9′-Bifluorenylidene-Based Conjugated Polymer." Polymers 15, no. 16 (August 10, 2023): 3360. http://dx.doi.org/10.3390/polym15163360.

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The synthesis of ladder-type 9,9′-bifluorenylidene-based conjugated polymer is reported. Unlike the typical synthetic strategy, the new designed ladder-type conjugated polymer is achieved via tandem Suzuki polymerization/Heck cyclization reaction in one-pot. In the preparation process, Suzuki polymerization reaction occurred first and then the intramolecular Heck cyclization followed smoothly under the same catalyst Pd(PPh3)4. The model reaction proved that the introduction of iodine (I) for this tandem reaction can effectively control the sequential bond-forming process and inhibit the additional competitive side reactions. Thus, small-molecule model compounds could be obtained in high yields. The successes of the synthesized small molecule and polymer compounds indicate that the Pd-catalyzed tandem reaction may be an effective strategy for improving extended π-conjugated materials.

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Helaja, Juho, and Richard Göttlich. "A new catalytic hetero-Heck type reaction." Chemical Communications, no. 7 (March 6, 2002): 720–21. http://dx.doi.org/10.1039/b201209j.

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Pirisedigh, Azadeh, Amin Zarei, Hojjat Seyedjamali, Leila Khazdooz, and Abdol R. Hajipour. "Heck-type reaction of aryldiazonium silica sulfates." Monatshefte für Chemie - Chemical Monthly 143, no. 5 (September 23, 2011): 791–95. http://dx.doi.org/10.1007/s00706-011-0632-1.

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Kitamura, Tsugio, and Yuzo Fujiwara. "ChemInform Abstract: Dehydrogenative Heck-Type Reactions: The Fujiwara-Moritani Reaction." ChemInform 46, no. 15 (March 26, 2015): no. http://dx.doi.org/10.1002/chin.201515342.

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Teng, Shenghan, Malcolm E. Tessensohn, Richard D. Webster, and Jianrong Steve Zhou. "Palladium-Catalyzed Intermolecular Heck-Type Reaction of Epoxides." ACS Catalysis 8, no. 8 (July 2, 2018): 7439–44. http://dx.doi.org/10.1021/acscatal.8b02029.

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Dissertations / Theses on the topic "Heck-type reaction"

1

Dumbre, D. K. "Selective liquid phase alcohol oxidation and heck- type coupling reactions using heterogeneous catalysts." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2008. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/2701.

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Roy, Amélie. "Synthetic studies of the formation of oxazoles and isoxazoles from N-acetoacetyl derivatives, scope and limitations ; and Aqueous rhodium-catalyzed Heck-type coupling reactions between boronic acids and olefins." Thesis, National Library of Canada = Bibliothèque nationale du Canada, 2000. http://www.collectionscanada.ca/obj/s4/f2/dsk1/tape3/PQDD_0021/MQ53366.pdf.

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Chang, Hsin-Yun, and 張馨云. "Synthetic Studies of Pseudouridine via Palladium-catalyzed Heck-type Glycosylation Reaction." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/58799143635724803610.

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碩士
國立臺灣師範大學
化學系
104
The nucleosidic bond of C-nucleosides are much more stable than N-nucleosides, which allows potential applications of C-nucleosides in medi-cinal chemistry and chemical biology. Some of the naturally occurring C-nucleosides possess a wide variety of biological activities. We are particu-larly interested in the synthesis of pseudouridine and 2’-deoxypseudouridine. In this thesis, we employed Heck-type coupling reactions to form C-C bonds between the anomeric carbon of 1, 2-unhydrous sugar derivatives and aryl iodides or iodo-heterocycles. Instead of utilizing toxic and expensive AsPh3 as the ligand, tour study has showed that the use of bidentate ligands for Heck-type coupling reactions were highly regio- and stereoselective. The methodology is applicable to the synthesis of 2’-deoxypseudouridine and pseudouridine.

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Tseng, Ya-Yi, and 曾雅怡. "Palladium-catalyzed Mizoroki-Heck Type Reaction of Diethyl Phosphonates and CuO/ZnO-catalyzed Three Component Coupling Reaction." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/6wgypd.

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碩士
國立臺北科技大學
有機高分子研究所
100
This thesis is composed of two parts. The first part is the palladium/cationic 2,2’-bipyridyl system catalyzed Mizoroki–Heck type reaction of arylboronic acids and diethyl phosphonates in water under air and the second part is the three component coupling reaction for the formation of propargyl amines catalyzed by ZnO supported CuO nanoparticle. We combine PdCl2(NH3)2 with cationic 2,2’-bipyridyl ligand as a catalytic system to catalyzed the coupling of arylboronic acids with diethyl vinylphosphonates or diethyl allylphosphonates resulting in the formation of corresponding Mizoroki–Heck type products. The reaction is high-yielding and high selectivity and can be performed in water under air, rendering it an environmentally-benign procedure. On the other hand, a ZnO supported CuO nanoparticle catalyst is prepared by simple procedure and can be applied as a heterogeneous catalyst for the coupling of alkyne, aldehyde, and amine leading to the formation of propargyl amine. The CuO/ZnO catalyst shows highly efficient for this three component coupling and the catalyst loading can be reduce to 0.01 mol% by up the scale to 70 mmol. After reaction, the catalyst can be recovered by simple centrifugation and reused for several times with only slight loss of it activity.

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Sherikar, Mahadev. "Construction of C-C bonds by C-H Activation: Rh(III)-Catalyzed reactions of Arenes and Heteroarenes with Maleimides and Allylic Alcohols." Thesis, 2021. https://etd.iisc.ac.in/handle/2005/5227.

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The thesis presents a few Rh-catalyzed C-H activations for the construction of C-C bonds. The difficulty of substitution or the arylation at the maleimide's double bond under C-H activation conditions prompted a detailed study on the reaction of maleimides with 3-trifluoromethyl ketone of indole. In this study, it was realized that switching the reactions between the Heck-type reaction and hydroarylation can be achieved by using basic or acid additives. A weakly coordinating carboxylate directing group assisted C-H activation with maleimides leading to a novel and switchable decarboxylative Heck-type and [4+1] annulation products catalyzed by Rh(III)-catalyst is investigated. In these reactions, solvents play a vital role in switching the selectivity. An aprotic solvent, THF, leads to the decarboxylative Heck-type product while the protic solvent, TFE, paves [4+1] annulation product. Allyl alcohol is chemically equivalent to α,β-unsaturated ketones, and aldehydes. A weakly coordinating carbonyl-directed coupling of allyl alcohols at the C-4 position of indole derivatives under the C-H activation conditions using an Rh(III)-catalyst has been explored. The product was transformed into a tricyclic derivative, which can serve as a potential precursor for synthesizing a few alkaloid molecules such as ergot, hapalindole alkaloids, and related heterocyclic compounds. A novel strategy, catalyzed by Rh(III), for synthesizing benzazepinone and azepinone derivatives by using allyl alcohol as a coupling partner has been studied. In this reaction, Rh(III) acts as a catalyst and oxidant. Under the reaction conditions, the allyl alcohol is in-situ converted to its carbonyl compound. The alkylated product obtained in the reaction further undergoes oxidative cyclization in the presence of Lewis acidic AgSbF6. The benzolactum obtained is a valuable intermediate to synthesize berberine-like analog dopamine D3 receptor ligand, which is a potential target in the treatment of neurological disorders.
Indian Institute of Science

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Chen, Shih-Chieh, and 陳世傑. "New Bis(fluoro-ponytailed) Bipyridine Ligands for the Pd-catalyzed Heck-type and Suzuki-type Reactions under Fluorous Biphasic and Thermomorphic conditions." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/22dvbb.

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碩士
國立臺北科技大學
有機高分子研究所
96
Five highly fluorinated bipyridine derivatives, (4,4’-bis(RfCH2OCH2)-2,2’-bpy), {Rf = n-C8F17(1a), n-C9F19(1b), n-C10F21(1c), n-C11F23(1d)} and (4,4’-bis(RfCH2CH2OCH2)-2,2’-bpy), {Rf = n-C8F17(1e)} have been synthesized using 4,4’-bis(bromomethylene)¬-2,2′-bpy and fluorinated alkoxides. The ligands have high fluorine contents and also high fluorophilicity, the partition ratio being 1：1.07, 1：1.04, 42：1, 70：1 and 6.56：1 for the FC 77/CH2Cl2 system, respectively. The reactions of ligands 1a-e with [Pd(CH3CN)2Cl2] result in new palladium complexes [PdCl2(4,4’-bis-(RfCH2OCH2)-2,2’-bpy)], where{Rf = n-C8F17(2a), n-C9F19(2b), n-C10F21(2c), n-C11F23(2d)}, and [PdCl2(4,4’-bis-(RfCH2CH2OCH2)-2,2’-bpy)], where{Rf = n-C8F17(2e)} respectively. Insoluble in organic solvents at room temp, the novel Pd complexes 2a-e dissolves in fluorinated solvents only, for instance FC77, which is mainly C8F18. The Pd complexes 2a-e have been successfully tested as the generic and recyclable catalysts in Heck-type and Suzuki-type reactions under the fluorous biphasic and thermomorphic conditions.

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7

Chang, Ting-Wei, and 張庭瑋. "Preparations of Secondary Phosphine Oxides Containing Indole Moiety and Their Derived Palladium Complexes: Applications in Heck-Type Catellani Reactions." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/56773684076508112642.

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碩士
國立中興大學
化學系所
103
Several new secondary phosphine oxides (SPOs) containing indole moiety were prepared. These new compounds are air- and moisture-stable preligands and advantageous for the purpose of storage. The structures of pallidium complexes might be stabilized by these SPOs. Pallidium complexes (3b & 4b) were obtained from the reactions of PdX2 (X = Cl, Br) with ligand (2b) and structures were determined by single-crystal X-ray diffraction methods. Applications of these SPO ligands (2a-2c) in palladium-catalyzed Heck-type Catellani reactions exhibited acceptable efficiencies. A extended mechanism was propsed to count the formations of all the organic products.

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Tomé, Sara Mirassol. "Synthesis of flavonoid-type compounds and sugar-substituted phenolics of pharmacological importance." Doctoral thesis, 2021. http://hdl.handle.net/10773/31390.

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Flavonoids are a large class of secondary metabolites widespread in the Plant Kingdom. These natural organic compounds possess a prominent interest as therapeutic agents. Among the vast range of biological properties of both natural and synthetic derivatives are their antioxidant and anti-inflammatory activities. Among the naturally occurring oxygen containing heterocyclic compounds, flavones (2-arylchromones) assume pronounced importance due to both their spread and diverse abundance as well as their well-known wide range of pharmacological properties. Halogenated derivatives of this privileged structure already proved to display enhanced biological activities and are also valuable frameworks as intermediates in the synthesis of more elaborated compounds, namely through metal cross-coupling reactions. Although several methods have already been developed towards the synthesis of haloflavones, there is still much room for improvement regarding the regioselectivity control of the halogenation process. The chemistry of this scarce group of natural compounds remains, therefore, an interesting challenge to organic chemists. Part of the work described in this thesis was focused on the synthesis of flavonoid-type compounds. Regarding the synthesis of flavones, synthetic pathways towards different substituted patterns of methoxy-, hydroxy- and chloroflavones were studied. The newly synthesised compounds were evaluated for their antioxidant, anti-inflammatory and antidiabetic properties and several of them exhibited remarkable activities including a great potential towards the treatment of type 2 diabetes mellitus. The structure–activity relationship study (SAR) of the prepared compounds was performed. Moreover, it were achieved the stereoselective synthesis of the novel (E,E)-aminoaurone-type compounds, as well as the preparation of different new analogues of iodophenyloxybenzaldeydes and iodoxanthones. Natural occurring phenolic compounds are frequently attached to carbohydrate moieties. The recognized prominent interest on C-glycosyl-substituted phenolic compounds in medicinal chemistry lies on the combination of the distinguishing hydrolytic stability of their C-glycosidic bond and the high hydrophilic character of the carbohydrate unit together with the well-known biological activities of phenolic compounds. Accordingly, the development of general approaches for the synthesis of C-glycosyl phenolic compounds is of great importance. In this thesis the study on the synthesis of C–C sugar-substituted phenolics is also described. The used synthetic strategy was based on the Heck cross coupling of vinylfuranose or vinylpyranose sugar scaffolds with different halophenolic frameworks. This straightforward wide in scope methodology lead to different types of phenolic-sugar hybrid molecules: phenoxybenzaldehyde–, xanthone–, chromone–, (E)-2-styrylchromone–, and (E,E)-aminoaurone-type– sugar hybrids. The unequivocal structural elucidation of all synthesised compounds was performed by 1D and 2D nuclear magnetic resonance experiments and supported by mass spectrometry and by either elemental analysis or high resolution mass spectrometry.
Os flavonoides são uma ampla família de metabolitos secundários ubíquos no Reino Vegetal. Estes compostos orgânicos de ocorrência natural têm sido alvo de grande interesse de estudo devido ao seu reconhecido potencial farmacológico. Entre as suas múltiplas propriedades biológicas destacam-se as atividades antioxidante e anti-inflamatória tanto de derivados naturais como de derivados sintéticos. No universo dos compostos heterocíclicos de oxigénio, as flavonas (2- arilcromonas) assumem especial importância devido à sua abundância, diversidade e amplo leque de propriedades farmacológicas às quais estão associadas. Alguns derivados halogenados desta estrutura molecular tão privilegiada provaram possuir atividades biológicas aprimoradas, sendo ainda valiosos intermediários na síntese de outros compostos orgânicos, nomeadamente mediante reações de acoplamento cruzado. Apesar de existirem vários métodos de síntese de haloflavonas, muito permanece ainda por desvendar relativamente ao controlo da regiosseletividade na halogenação. Parte do trabalho descrito nesta tese centrou-se na síntese de compostos do tipo flavonoide. Foram desenvolvidas novas rotas de síntese para a obtenção de novas flavonas com diferentes padrões de substituição: flavonas metoxiladas, hidroxiladas e cloradas em várias posições do seu esqueleto carbonado. Foi efetuada a avaliação biológica destes compostos assim como o estudo da relação estrutura–atividade (SAR), tendo alguns derivados exibido atividades antioxidante e anti-inflamatória muito satisfatórias e comprovado potencial no tratamento da diabetes mellitus tipo 2. Foram ainda estudadas a síntese estereoesseletiva de novos derivados do tipo (E,E)-aminoaurona e a preparação de novos análogos de iodofeniloxibenzaldeídos e iodoxantonas. Na natureza os compostos fenólicos encontram-se frequentemente associados a unidades de hidratos de carbono. No âmbito da química medicinal, o reconhecido e crescente interesse nos compostos fenólicos C-glicosilados advém da combinação de várias caraterísticas vantajosas a estes inerentes: a distinta estabilidade hidrolítica da ligação C-glicosídica, o elevado caráter hidrofílico proporcionado pelas unidades de açúcar e ainda tudo isto associado à reconhecida importância biológica dos compostos fenólicos. Nesta dissertação é também descrito o estudo efetuado no âmbito da síntese de novos compostos fenólicos substituídos por unidades de açúcar mediante ligações C–C. Para tal, foram preparados derivados vinilados de açúcar (do tipo furanose e piranose) e também derivados halofenólicos do tipo fenoxibenzaldeído, xantona, cromona, (E)-2-estirilcromona e (E,E)- aminoaurona. Tendo como estratégia-chave a reação de acoplamento cruzado de Heck, foi possível a síntese de vários novos derivados fenólicos contendo unidades de açúcar. A elucidação estrutural inequívoca de todos os compostos sintetizados foi efetuada através da espetroscopia de ressonância magnética nuclear 1D e 2D e sustentada pela análise de espetrometria de massa, análise elementar ou espetrometria de massa de alta resolução.
Programa Doutoral em Química

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Liang, Ya-Han, and 梁雅涵. "Preparation and Application of Cyclic 1,2-Diamino Derivatives and N-P-N Type Secondary Phosphine Oxides as Ligands in Palladium Complexes Catalyzed Suzuki-Miyaura and Heck Cross-coupling Reactions." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/03530131034773777292.

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碩士
國立中興大學
化學系所
100
A series of 1,2-diaminocyclohexane and o-phenylenediamine derivatives as diamine ligands (3a-3h) were prepared, and further reactions led to the formation of secondary phosphine oxides (SPOs, 4a-4c).The molecular structures of 4c and complexes 3a_Pd, 3b_Pd, 3c_Pd, 3d_Cu were determined by single crystal X-ray diffraction methods. After screening of the ligands, diamines showed better coordinating capacities toward the palladium salt. These ligands can stabilize the palladium complexes during the catalytic reactions. Catalysis of the Suzuki-Miyaura coupling reactions with 3a for the aryl bromides showed good yields, nevertheless, lower reactivities were observed for aryl chlorides. In addition, 3d was employed in the Heck reaction as ligand. It exhibited a good tolerance of functional groups for the aryl bromides.

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Books on the topic "Heck-type reaction"

1

Wolfe, J. P. (James Philip), 1943- and Larhed Mats, eds. Science of synthesis: Cross coupling and Heck-type reactions. Stuttgart: Georg Thieme Verlag KG, 2013.

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Cross Coupling and Heck-Type Reactions. Thieme Medical Publishers, Incorporated, 2013.

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Cross Coupling and Heck-Type Reactions 3: Metal-Catalyzed Heck-Type Reactions and C-C Cross Coupling Via C-H Activation. Thieme Medical Publishers, Incorporated, 2013.

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Molander, Gary A., Carl P. Decicco, and Alois Fürstner. Cross Coupling and Heck-Type Reactions Vol. 1: C-C Cross Coupling Using Organometallic Partners. Thieme Medical Publishers, Incorporated, 2013.

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Carreira, Erick M., Carl P. Decicco, John P. Wolfe, Mats Larhed, and Alois Fürstner. Cross-Coupling and Heck-Type Reactions 2: Carbon-Heteroatom Cross Coupling and C-C Cross Couplings of Acidic C-H Nucleophiles. Thieme Medical Publishers, Incorporated, 2013.

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Roy, Amelie. Synthetic studies of the formation of oxazoles and isoxazoles from N-acetoacetyl derivatives: Scope and limitations AND Aqueous rhodium-catalyzed Heck-type coupling reactions between boronic acids and olefins. 2000.

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Book chapters on the topic "Heck-type reaction"

1

Oshima, K. "Heck-type Reaction." In Compounds of Groups 15 (As, Sb, Bi) and Silicon Compounds, 1. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-004-00789.

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Lei, A., and S. Tang. "47.1.2.1.6 Alkyl-Mizoroki–Heck-Type Reactions." In Knowledge Updates 2023/1. Stuttgart: Georg Thieme Verlag KG, 2023. http://dx.doi.org/10.1055/sos-sd-147-00132.

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AbstractSubstituted alkenes are basic structural motifs in a large number of organic molecules and their synthesis has received continuous attention from synthetic chemists. One of the most straightforward methods for constructing substituted alkenes is the Mizoroki–Heck reaction. Generally, this transformation is catalyzed by palladium and mainly deals with the synthesis of substituted alkenes from aryl or vinyl electrophiles. In sharp contrast, the Mizoroki–Heck reaction of alkyl electrophiles has long been considered a challenging transformation due to the decreased rates of oxidative addition and subsequent facile β-hydride elimination. To address this limitation in traditional Mizoroki–Heck reactions, radical processes have been introduced to achieve the alkenylation of alkyl electrophiles. This review provides an overview of the recent developments in alkyl-Mizoroki–Heck-type reactions. Particular attention is paid to the intermolecular Mizoroki–Heck-type reaction between alkyl radicals and terminal alkenes. The limitations and advantages of using different catalytic methods are discussed and compared.

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"Cyclic Alkenes as Reaction Components." In Cross Coupling and Heck-Type Reactions 3, edited by Larhed and Odell. Stuttgart: Georg Thieme Verlag, 2013. http://dx.doi.org/10.1055/sos-sd-209-00157.

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"Electron-Rich Alkenes as Reaction Components." In Cross Coupling and Heck-Type Reactions 3, edited by Larhed and Odell. Stuttgart: Georg Thieme Verlag, 2013. http://dx.doi.org/10.1055/sos-sd-209-00099.

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"Reaction with (Het)Arylmetals or (Het)Arenes." In Cross Coupling and Heck-Type Reactions 3, edited by Larhed and Odell. Stuttgart: Georg Thieme Verlag, 2013. http://dx.doi.org/10.1055/sos-sd-209-00031.

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"Reaction with Nonaromatic Halides, Sulfonates, or Related Compounds." In Cross Coupling and Heck-Type Reactions 3, edited by Larhed and Odell. Stuttgart: Georg Thieme Verlag, 2013. http://dx.doi.org/10.1055/sos-sd-209-00054.

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"Reaction with Nonaromatic Alkenyl Halides or Alkenyl Sulfonates." In Cross Coupling and Heck-Type Reactions 3, edited by Larhed and Odell. Stuttgart: Georg Thieme Verlag, 2013. http://dx.doi.org/10.1055/sos-sd-209-00144.

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"Alkenes with Metal-Directing Groups as Reaction Components." In Cross Coupling and Heck-Type Reactions 3, edited by Larhed and Odell. Stuttgart: Georg Thieme Verlag, 2013. http://dx.doi.org/10.1055/sos-sd-209-00173.

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"Alkenes with Allylic Substitution and Homologues as Reaction Components." In Cross Coupling and Heck-Type Reactions 3, edited by Larhed and Odell. Stuttgart: Georg Thieme Verlag, 2013. http://dx.doi.org/10.1055/sos-sd-209-00070.

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"Reaction with Arylboronic Acids or Derivatives or Aroyl Halides." In Cross Coupling and Heck-Type Reactions 3, edited by Larhed and Odell. Stuttgart: Georg Thieme Verlag, 2013. http://dx.doi.org/10.1055/sos-sd-209-00130.

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