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1

Le Gall, Erwan, Jérôme Paul, Marc Presset, Eric Léonel, and Pascal Retailleau. "Insights into the Cobalt-Catalyzed Three-Component Coupling of Mixed Aromatic Organozinc Species, Carbonyl Compounds or Imines and Michael Acceptors: Synthetic and Mechanistic Aspects." Synthesis 50, no. 02 (2017): 254–66. http://dx.doi.org/10.1055/s-0036-1590957.

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The first examples of cobalt-catalyzed multicomponent couplings of mixed aromatic arylzinc reagents with Michael acceptors and carbonyl compounds or imines is described. The reaction system employs a cobalt(II)-2,2′-bipyridine or a cobalt(II)-1,10-phenanthroline complex as a catalyst for both organozinc generation and subsequent multicomponent assembly by formal Michael addition/aldol coupling or Mannich reaction. This study brings new insights into the synthetic scope and mechanism of the reaction.
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2

Yang, Hongwei, Huanhe Dong, Baoshu Yin, and Zhenyu Liu. "Nonlinear Bi-Integrable Couplings of Multicomponent Guo Hierarchy with Self-Consistent Sources." Advances in Mathematical Physics 2012 (2012): 1–14. http://dx.doi.org/10.1155/2012/272904.

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Based on a well-known Lie algebra, the multicomponent Guo hierarchy with self-consistent sources is proposed. With the help of a set of non-semisimple Lie algebra, the nonlinear bi-integrable couplings of the multicomponent Guo hierarchy with self-consistent sources are obtained. It enriches the content of the integrable couplings of hierarchies with self-consistent sources. Finally, the Hamiltonian structures are worked out by employing the variational identity.
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3

Lu, Fu-Dong, Gui-Feng He, Liang-Qiu Lu, and Wen-Jing Xiao. "Metallaphotoredox catalysis for multicomponent coupling reactions." Green Chemistry 23, no. 15 (2021): 5379–93. http://dx.doi.org/10.1039/d1gc00993a.

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The key advances in the field of metallaphotoredox-catalyzed multicomponent couplings in recent years are highlighted in this review. To better meet the needs of modern chemistry, further research outlooks were also proposed.
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4

Fereyduni, Ehsan, Jacob N. Sanders, Gabriel Gonzalez, K. N. Houk, and Alexander J. Grenning. "Transient [3,3] Cope rearrangement of 3,3-dicyano-1,5-dienes: computational analysis and 2-step synthesis of arylcycloheptanes." Chemical Science 9, no. 46 (2018): 8760–64. http://dx.doi.org/10.1039/c8sc03057j.

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5

Odell, Luke, Mats Larhed, and Linda Åkerbladh. "Palladium-Catalyzed Molybdenum Hexacarbonyl-Mediated Gas-Free Carbonylative Reactions." Synlett 30, no. 02 (2018): 141–55. http://dx.doi.org/10.1055/s-0037-1610294.

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This account summarizes Pd(0)-catalyzed Mo(CO)6-mediated gas-free carbonylative reactions published in the period October 2011 to May 2018. Presented reactions include inter- and intramolecular carbonylations, carbonylative cross-couplings, and carbonylative multicomponent reactions using Mo(CO)6 as a solid source of CO. The presented methodologies were developed mainly for small-scale applications, avoiding the problematic use of gaseous CO in a standard laboratory. In most cases, the reported Mo(CO)6-mediated carbonylations were conducted in sealed vials or by using two-chamber solutions.1 I
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6

Xia, Tiecheng, and Engui Fan. "The multicomponent generalized Kaup–Newell hierarchy and its multicomponent integrable couplings system with two arbitrary functions." Journal of Mathematical Physics 46, no. 4 (2005): 043510. http://dx.doi.org/10.1063/1.1866220.

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7

Liu, Lei, Maria Camila Aguilera, Wes Lee, Cassandra R. Youshaw, Michael L. Neidig, and Osvaldo Gutierrez. "General method for iron-catalyzed multicomponent radical cascades–cross-couplings." Science 374, no. 6566 (2021): 432–39. http://dx.doi.org/10.1126/science.abj6005.

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Iron links a trio Iron holds particular appeal as a catalytic metal—it is safe and abundant, as well as a mainstay of enzymatic reactivity. Nonetheless, in synthetic construction of carbon-carbon bonds, modern chemists have largely had to rely on rarer metals such as palladium. Liu et al . now report that coordination of iron by a bulky chelating phosphine ligand enables efficient mutual coupling of three different reactants—an alkyl halide, an aryl Grignard, and an olefin—to form two carbon-carbon bonds (see the Perspective by Lefèvre). A combination of Mössbauer spectroscopy, crystallography
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8

Odom, Aaron L., and Tanner J. McDaniel. "Titanium-Catalyzed Multicomponent Couplings: Efficient One-Pot Syntheses of Nitrogen Heterocycles." Accounts of Chemical Research 48, no. 11 (2015): 2822–33. http://dx.doi.org/10.1021/acs.accounts.5b00280.

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9

El Kaim, Laurent, Marie Gizolme, Laurence Grimaud, and Julie Oble. "Direct Access to Heterocyclic Scaffolds by New Multicomponent Ugi−Smiles Couplings." Organic Letters 8, no. 18 (2006): 4019–21. http://dx.doi.org/10.1021/ol061605o.

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10

Smith, Amos B., and Armen M. Boldi. "Multicomponent Linchpin Couplings of Silyl Dithianes via Solvent-Controlled Brook Rearrangement." Journal of the American Chemical Society 119, no. 29 (1997): 6925–26. http://dx.doi.org/10.1021/ja970371o.

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11

Yu, Fajun, and Hongqing Zhang. "Hamiltonian structure of the integrable couplings for the multicomponent Dirac hierarchy." Applied Mathematics and Computation 197, no. 2 (2008): 828–35. http://dx.doi.org/10.1016/j.amc.2007.08.017.

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12

Campos, Catherine A., Joseph B. Gianino та Brandon L. Ashfeld. "Bifunctional Titanocene Catalysis in Multicomponent Couplings: A Convergent Assembly of β-Alkynyl Ketones". Organic Letters 15, № 11 (2013): 2656–59. http://dx.doi.org/10.1021/ol400943a.

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13

SMITH, A. B. III, and A. M. BOLDI. "ChemInform Abstract: Multicomponent Linchpin Couplings of Silyl Dithianes via Solvent- Controlled Brook Rearrangement." ChemInform 28, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.199744171.

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14

El Kaïm, Laurent, Marie Gizolme, Laurence Grimaud, and Julie Oble. "Smiles Rearrangements in Ugi- and Passerini-Type Couplings: New Multicomponent Access toO- andN-Arylamides." Journal of Organic Chemistry 72, no. 11 (2007): 4169–80. http://dx.doi.org/10.1021/jo070202e.

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15

Rong, Ben-Guang, and Andrzej Kraslawski. "Optimal Design of Distillation Flowsheets with a Lower Number of Thermal Couplings for Multicomponent Separations." Industrial & Engineering Chemistry Research 41, no. 23 (2002): 5716–26. http://dx.doi.org/10.1021/ie0107136.

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16

Campos, Catherine A., Joseph B. Gianino та Brandon L. Ashfeld. "ChemInform Abstract: Bifunctional Titanocene Catalysis in Multicomponent Couplings: A Convergent Assembly of β-Alkynyl Ketones." ChemInform 44, № 40 (2013): no. http://dx.doi.org/10.1002/chin.201340064.

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17

Andraos, John. "A new paradigm for designing ring construction strategies for green organic synthesis: implications for the discovery of multicomponent reactions to build molecules containing a single ring." Beilstein Journal of Organic Chemistry 12 (November 16, 2016): 2420–42. http://dx.doi.org/10.3762/bjoc.12.236.

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A new way of developing novel synthesis strategies for the construction of monocyclic rings found in organic molecules is presented. The method is based on the visual application of integer partitioning to chemical structures. Two problems are addressed: (1) the determination of the total number of possible ways to construct a given ring by 2-, 3-, and 4-component couplings; and (2) the systematic enumeration of those possibilities. The results of the method are illustrated using cyclohexanone, pyrazole, and the Biginelli adduct as target ring systems with a view to discover new and greener st
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18

El Kaïm, Laurent, and Laurence Grimaud. "The Ugi-Smiles and Passerini-Smiles Couplings: A Story About Phenols in Isocyanide-Based Multicomponent Reactions." European Journal of Organic Chemistry 2014, no. 35 (2014): 7749–62. http://dx.doi.org/10.1002/ejoc.201402783.

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19

YAMAMOTO, RYOICHI, YASUYA NAKAYAMA, and KANG KIM. "SMOOTHED PROFILE METHOD TO SIMULATE COLLOIDAL PARTICLES IN COMPLEX FLUIDS." International Journal of Modern Physics C 20, no. 09 (2009): 1457–65. http://dx.doi.org/10.1142/s0129183109014515.

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A new direct numerical simulation scheme, called "Smoothed Profile (SP) method," is presented. The SP method, as a direct numerical simulation of particulate flow, provides a way to couple continuum fluid dynamics with rigid-body dynamics through smoothed profile of colloidal particle. Our formulation includes extensions to colloids in multicomponent solvents such as charged colloids in electrolyte solutions. This method enables us to compute the time evolutions of colloidal particles, ions, and host fluids simultaneously by solving Newton, advection-diffusion, and Navier–Stokes equations so t
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20

El Kaim, Laurent, and Laurence Grimaud. "ChemInform Abstract: The Ugi-Smiles and Passerini-Smiles Couplings: A Story About Phenols in Isocyanide-Based Multicomponent Reactions." ChemInform 46, no. 9 (2015): no. http://dx.doi.org/10.1002/chin.201509306.

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21

Smith, Amos B., and Suresh M. Pitram. "Multicomponent Linchpin Couplings of Silyl Dithianes: Synthesis of the Schreiber C(16−28) Trisacetonide Subtarget for Mycoticins A and B." Organic Letters 1, no. 12 (1999): 2001–4. http://dx.doi.org/10.1021/ol991166b.

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22

Lee, Sunwoo, and Muhammad Aliyu Idris. "Recent Advances in Decarboxylative Reactions of Alkynoic Acids." Synthesis 52, no. 16 (2020): 2277–98. http://dx.doi.org/10.1055/s-0040-1707600.

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Alkynoic acids have been widely employed as alkyne and alkene sources in decarboxylative reactions. Alkynoic acid coupling leads to the formation of direct coupling products and cyclized products through sequential reactions. Moreover, homocoupling and multicomponent reactions have been developed. The decarboxylative addition of alkynoic acids generates the corresponding alkene products. A number of synthetic methods are utilized for the preparation of arylpropynoic acids including the Sonogashira coupling and the carboxylation of terminal alkynes. Recently, the use of decarboxylative halogena
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23

Smith, Amos B., Suresh M. Pitram, Armen M. Boldi, Matthew J. Gaunt, Chris Sfouggatakis, and William H. Moser. "Multicomponent Linchpin Couplings. Reaction of Dithiane Anions with Terminal Epoxides, Epichlorohydrin, and Vinyl Epoxides: Efficient, Rapid, and Stereocontrolled Assembly of Advanced Fragments for Complex Molecule Synthesis." Journal of the American Chemical Society 125, no. 47 (2003): 14435–45. http://dx.doi.org/10.1021/ja0376238.

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24

Lee, Daesung, and Sourav Ghorai. "Aryne-Based Multicomponent Coupling Reactions." Synlett 31, no. 08 (2020): 750–71. http://dx.doi.org/10.1055/s-0039-1690824.

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Multicomponent reactions (MCRs) constitute a powerful synthetic tool to generate a large number of small molecules with high atom economy, which thus can efficiently expand the chemical space with molecular diversity and complexity. Aryne-based MCRs offer versatile possibilities to construct functionalized arenes and benzo-fused heterocycles. Because of their electrophilic nature, arynes couple with a broad range of nucleophiles. Thus, a variety of aryne-based MCRs have been developed, the representative of which are summarized in this account.1 Introduction2 Aryne-Based Multicomponent Reactio
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25

Häusler, Mauro, Cedric Schmelzbach, and David Sollberger. "The Galperin source: A novel efficient multicomponent seismic source." GEOPHYSICS 83, no. 6 (2018): P19—P27. http://dx.doi.org/10.1190/geo2018-0020.1.

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Multicomponent acquisition enables a more complete observation of the seismic wavefield compared with single-component measurements and has therefore experienced increased interest in the past few decades. Whereas the use of multicomponent receivers is well-established, efficient and effective multicomponent sources are still difficult to realize. One of the main drawbacks of common multicomponent sources is that the source coupling differs for different components. Differences in the source coupling can lead to amplitude variations introducing uncertainties when jointly analyzing data from tw
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26

Uchida, Keisuke, Suguru Yoshida, and Takamitsu Hosoya. "Synthetic Aryne Chemistry toward Multicomponent Coupling." Journal of Synthetic Organic Chemistry, Japan 77, no. 2 (2019): 145–62. http://dx.doi.org/10.5059/yukigoseikyokaishi.77.145.

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27

Balme, Genevi�ve. "Pyrrole Syntheses by Multicomponent Coupling Reactions." Angewandte Chemie International Edition 43, no. 46 (2004): 6238–41. http://dx.doi.org/10.1002/anie.200461073.

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28

Pan, Na, Johanne Ling, Ramiro Zapata, Jean-Pierre Pulicani, Laurence Grimaud та Maxime R. Vitale. "Electrochemical TEMPO-catalyzed multicomponent C(sp3)–H α-carbamoylation of free cyclic secondary amines". Green Chemistry 21, № 22 (2019): 6194–99. http://dx.doi.org/10.1039/c9gc03173a.

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29

Ruscoe, Rebecca E., Michael Callingham, Joshua A. Baker, Stamatis E. Korkis, and Hon Wai Lam. "Iridium-catalyzed 1,5-(aryl)aminomethylation of 1,3-enynes by alkenyl-to-allyl 1,4-iridium(i) migration." Chemical Communications 55, no. 6 (2019): 838–41. http://dx.doi.org/10.1039/c8cc09238a.

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30

YU, FA-JUN. "ADJOINT SYMMETRY CONSTRAINTS AND INTEGRABLE COUPLING SYSTEM OF MULTICOMPONENT KN EQUATIONS." International Journal of Modern Physics B 25, no. 21 (2011): 2841–52. http://dx.doi.org/10.1142/s0217979211100837.

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A soliton hierarchy of multicomponent KN equations is generated from an arbitrary order matrix spectral problem, along with its bi-Hamiltonian formulation. Adjoint symmetry constraints are presented to manipulate binary nonlinearization for the associated arbitrary order matrix spectral problem. Finally, a class of integrable coupling systems of the multicomponent KN soliton equation hierarchy is obtained using Ma's method associated with enlarging spectral problems [W. X. Ma, Phys. Lett. A316, 72–76 (2003)].
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31

Krishna, Rajamani. "Uphill diffusion in multicomponent mixtures." Chemical Society Reviews 44, no. 10 (2015): 2812–36. http://dx.doi.org/10.1039/c4cs00440j.

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Diffusional coupling effects may cause uphill transport of a species against its concentration gradient. Transient overshoots and serpentine equilibration trajectories in composition space are fingerprints of uphill diffusion. Serpentine diffusion trajectories may enter meta-stable zones, leading to spontaneous emulsification and the Ouzo effect.
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32

Yao, Liangliang, Qiong Hu, Yu Lei, Li Bao, and Yimin Hu. "C–O/C–S difunctionalized benzene derivatives via multicomponent coupling of tetraynes." Organic Chemistry Frontiers 7, no. 22 (2020): 3633–37. http://dx.doi.org/10.1039/d0qo00967a.

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33

Zhong, Jing, Kai Wang, and Li Jun Zhang. "A Coupling Interface between Phase-Field Model with Finite Interface Dissipation and CALPHAD Thermodynamic and Atomic Mobility Databases." Defect and Diffusion Forum 383 (February 2018): 66–73. http://dx.doi.org/10.4028/www.scientific.net/ddf.383.66.

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A coupling interface between phase-field model with finite interface dissipation and the CALPHAD (CALculation of PHAse Diagram) thermodynamic and atomic mobility databases is developed. It robotizes the procedures that provides the composition and temperature dependent properties in multicomponent and multi-phase systems. Based on the developed coupling interface, different CALPHAD properties can be directly coupling in the phase-field simulation.
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34

Visbal, Renso, Sara Graus, Raquel P. Herrera, and M. Concepción Gimeno. "Gold Catalyzed Multicomponent Reactions beyond A3 Coupling." Molecules 23, no. 9 (2018): 2255. http://dx.doi.org/10.3390/molecules23092255.

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The preparation of complex architectures has inspired the search for new methods and new processes in organic synthesis. Multicomponent reactions have become an interesting approach to achieve such molecular diversity and complexity. This review intends to illustrate important gold-catalyzed examples for the past ten years leading to interesting skeletons involved in biologically active compounds.
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35

Arai, Takayoshi, Yui Ikematsu, and Yuuki Suemitsu. "Nickel-catalyzed multicomponent coupling reaction using ynones." Pure and Applied Chemistry 82, no. 7 (2010): 1485–90. http://dx.doi.org/10.1351/pac-con-09-09-08.

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Conjugate addition of Me3SiCN to ynones is smoothly catalyzed by Ni(cod)2 to give β-cyano-silyloxyallenes quantitatively. Subsequent treatment of the silyloxyallenes with N-bromo succinimide (NBS) provides the tetrasubstituted α-bromo-β-cyanoenones in high yields (up to 95 %) with excellent Z-selectivity (E/Z = up to >1/99). X-ray crystallographic analysis shows a bent structure of the α-bromo-β-cyanoenone due to deconjugation of the π-bond and the carbonyl group. Furthermore, three-component coupling reactions of ynones, dialkylzinc, and alde-hydes are catalyzed by Ni(cod)2 to provide tetr
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36

Ohashi, Masato, Yoichi Hoshimoto, and Sensuke Ogoshi. "Aza-nickelacycle key intermediate in nickel(0)-catalyzed transformation reactions." Dalton Transactions 44, no. 27 (2015): 12060–73. http://dx.doi.org/10.1039/c5dt00640f.

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37

KASAMATSU, KENICHI, MAKOTO TSUBOTA, and MASAHITO UEDA. "VORTICES IN MULTICOMPONENT BOSE–EINSTEIN CONDENSATES." International Journal of Modern Physics B 19, no. 11 (2005): 1835–904. http://dx.doi.org/10.1142/s0217979205029602.

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We review the topic of quantized vortices in multicomponent Bose–Einstein condensates of dilute atomic gases, with an emphasis on the two-component condensates. First, we review the fundamental structure, stability and dynamics of a single vortex state in a slowly rotating two-component condensates. To understand recent experimental results, we use the coupled Gross–Pitaevskii equations and the generalized nonlinear sigma model. An axisymmetric vortex state, which was observed by the JILA group, can be regarded as a topologically trivial skyrmion in the pseudospin representation. The internal,
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38

Shintani, Ryo, Takafumi Yamagami, and Tamio Hayashi. "Rhodium-Catalyzed Multicomponent-Coupling Reactions Involving a Carborhodation−Cross-Coupling Sequence." Organic Letters 8, no. 21 (2006): 4799–801. http://dx.doi.org/10.1021/ol061858h.

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39

Roy, Tony, Sachin Suresh Bhojgude, Trinadh Kaicharla, Manikandan Thangaraj, Bikash Garai, and Akkattu T. Biju. "Employing carboxylic acids in aryne multicomponent coupling triggered by aziridines/azetidines." Organic Chemistry Frontiers 3, no. 1 (2016): 71–76. http://dx.doi.org/10.1039/c5qo00328h.

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The transition-metal-free aryne multicomponent coupling (MCC) involving carboxylic acids initiated by aziridines/azetidines leading to the synthesis of N-aryl β/γ-amino alcohol derivatives has been developed.
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40

Horwitz, Matthew A., Naoya Tanaka, Takuya Yokosaka, Daisuke Uraguchi, Jeffrey S. Johnson, and Takashi Ooi. "Enantioselective reductive multicomponent coupling reactions between isatins and aldehydes." Chemical Science 6, no. 11 (2015): 6086–90. http://dx.doi.org/10.1039/c5sc02170g.

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A reductive coupling of two different carbonyls via a polar two-electron reaction mechanism was developed and the stereochemical outcome of this multicomponent process is precisely controlled by a chiral triaminoiminophosphorane.
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41

Kimura, Masanari, Yasuyuki Mori, Chieko Shigeno, Ying Luo, Bun Chan, and Gen Onodera. "Ni-Catalyzed Formal Carbonyl-Ene Reaction of Terminal Alkenes via Carbon Dioxide Insertion." Synlett 29, no. 06 (2017): 742–46. http://dx.doi.org/10.1055/s-0036-1591845.

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Nickel catalyzes the multicomponent coupling reaction of terminal alkenes, carbon dioxide, and organoaluminum reagents, leading to the synthesis of homoallylic alcohols in moderate-to-good yields with excellent regio- and stereoselectivities.
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42

Aboonajmi, Jasem, Masoumeh Mohammadi, Farhad Panahi, Mahdi Aberi, and Hashem Sharghi. "One-pot, three-component, iron-catalyzed synthesis of benzimidazoles via domino C–N bond formation." RSC Advances 13, no. 35 (2023): 24789–94. http://dx.doi.org/10.1039/d3ra04450e.

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A one-pot multicomponent procedure for the efficient synthesis of benzimidazole derivatives via coupling of benzo-1,2-quinone, aldehydes, and ammonium acetate using an Fe(iii)-porphyrin catalyst system is presented.
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43

Mardjan, Muhammad Idham Darussalam, Jean Luc Parrain та Laurent Commeiras. "Copper-Catalyzed-Multicomponent Reaction towards the Synthesis of γ-Hydroxybutyrolactams". Materials Science Forum 1061 (26 травня 2022): 151–56. http://dx.doi.org/10.4028/p-yux0t7.

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Copper-catalyzed-multicomponent reaction has been applied to prepare several examples γ-hydroxybutyrolactams. The synthesis of γ-hydroxybutyrolactams occurred via cascade sequence comprising Sonogashira coupling, heterocyclization and nucleophilic addition reactions. The reaction involved the starting materials of (Z)-3-iodobutenoic acid, terminal alkynes and butylamine. The results showed that electronic effect of terminal alkynes played important role in synthesis of γ-hydroxybutyrolactams. The multicomponent reaction allowed us to obtain the desired products and to create multiple bonds in
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44

Atar, Amol Balu, Jongmin Kang, and Arvind H. Jadhav. "A [bmim]Cl-promoted domino protocol using an isocyanide-based [4+1]-cycloaddition reaction for the synthesis of diversely functionalized 3-alkylamino-2-alkyl/aryl/hetero-aryl indolizine-1-carbonitriles under solvent-free conditions." New Journal of Chemistry 44, no. 8 (2020): 3241–48. http://dx.doi.org/10.1039/c9nj05738b.

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A room temperature-based ionic liquid [bmim]Cl-catalyzed multicomponent coupling strategy for the synthesis of 3-alkylamino-2-alkyl/aryl/hetero-aryl indolizine-1-carbonitrile derivatives under mild conditions is shown.
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45

Landschulze, Marcus, Rolf Mjelde, and Karin Landschulze. "Systematic simulation of multicomponent receiver coupling to the seafloor using rheological models." GEOPHYSICS 79, no. 6 (2014): P9—P19. http://dx.doi.org/10.1190/geo2013-0329.1.

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This paper reports a comparison of three different rheological models used to characterize receiver coupling to the seafloor. We used a finite-element simulation tool to simulate the mechanical receiver coupling to the seafloor as a viscoelastic system with a combination of linear elastic springs and linear viscous dashpots, known as rheological models. Three models cover most of all mechanic coupling systems, the most commonly applied Kelvin-Voigt model (KVM), the Maxwell model (MM), and the standard linear solid (SLS) model. The models differ in behavior for different coupling aspects such a
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46

Rebelo, Jordan, Steffen Kress, Adam Friedman, and Mark Lautens. "Orthogonally Reacting Boron Coupling Reagents: A Novel Multicomponent-Multicatalytic Reaction [(MC)2R] of Dichlorovinylpyrazine." Synthesis 48, no. 19 (2016): 3155–64. http://dx.doi.org/10.1055/s-0035-1561670.

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The results presented herein illustrate the feasibility of two orthogonally reacting boron coupling reagents as a new control strategy in multicomponent-multicatalytic reaction [(MC)2R] chemistry. A process employing dichlorovinylpyrazine merging the rhodium-catalyzed hydroarylation with the Suzuki coupling has been discovered. Three new bonds are formed in a one-pot, one-step process efficiently providing highly substituted diaza-dihydrodibenzoxepine products.
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47

Henderson, Jaclyn L., Andrew S. Edwards, and Michael F. Greaney. "Biaryl Synthesis via Palladium-Catalyzed Aryne Multicomponent Coupling." Organic Letters 9, no. 26 (2007): 5589–92. http://dx.doi.org/10.1021/ol702584t.

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48

Gianino, Joseph B., and Brandon L. Ashfeld. "Titanocene-Catalyzed Multicomponent Coupling Approach to Diarylethynyl Methanes." Journal of the American Chemical Society 134, no. 44 (2012): 18217–20. http://dx.doi.org/10.1021/ja308891e.

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49

Mills, R., A. Perera, J. P. Simonin, L. Orcil, and P. Turq. "Coupling of diffusion processes in multicomponent electrolyte solutions." Journal of Physical Chemistry 89, no. 13 (1985): 2722–25. http://dx.doi.org/10.1021/j100259a003.

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Bhojgude, Sachin Suresh, and Akkattu T. Biju. "Arynes in Transition-Metal-Free Multicomponent Coupling Reactions." Angewandte Chemie International Edition 51, no. 7 (2012): 1520–22. http://dx.doi.org/10.1002/anie.201106984.

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