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Artículos de revistas sobre el tema "Diazabutadienes"

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Publicado: 6 de septiembre de 2023

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1

Romero-Ortega, Moisés, Ignacio Medina-Mercado, Ivann Zaragoza-Galicia y Horacio Olivo. "2-Trifluoromethyl-1,3-diazabutadienes as Useful Intermediates for the Construction of 2-Trifluoromethylpyrimidine Derivatives". Synthesis 50, n.º 20 (16 de julio de 2018): 4133–39. http://dx.doi.org/10.1055/s-0037-1610444.

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A methodology to prepare 2-trifluoromethylpyrimidines has been developed on the basis of a cyclization reaction of 2-trifluoromethyl-1,3-diazabutadienes. These 2-trifluoromethyl-1,3-diazabutadienes were prepared by the condensation of trifluoroacetamidine and amide acetals or with chloromethaniminium salt derived from N,N-dimethylbenzamide with phosphorus oxychloride. The cycloaddition reactions of these 2-trifluoromethyl-1,3-diazabutadienes with DMAD and phenylacetyl chloride provided 2-trifluoromethylpyrimidine derivatives in regular to moderate overall yield.
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2

Romero-Ortega, Moisés, Michelle Trujillo-Lagunas, Ignacio Medina-Mercado, Ivann Zaragoza-Galicia y Horacio Olivo. "A Synthesis of 4-Chloro-2-(trichloromethyl)pyrimidines and Their Study in Nucleophilic Substitution". Synthesis 51, n.º 02 (11 de septiembre de 2018): 530–37. http://dx.doi.org/10.1055/s-0037-1610270.

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A convenient two-step, one-pot synthesis of 4-chloro-2-(trichloromethyl)pyrimidines starting from 2-(trichloromethyl)-1,3-diazabutadienes is described. These nitrogen heterocycles were prepared by a sequential acylation/intramolecular cyclization reaction between 2-(trichloromethyl)-1,3-diazabutadienes and acyl chlorides in the presence of triethylamine followed by treatment with POCl3. This is the first report for the synthesis of this type of 4-chloro-2-(trichloromethyl)pyrimidine derivatives and serves as a source for a wide variety of other substituted pyrimidines by nucleophilic substitution reactions.
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3

Sain, Bir, Satyendra P. Singh y Jagir S. Sandhu. "Diazabutadienes in heterocyclic syntheses: reaction of 1,3-diazabutadienes with 2-oxazolin-5-ones". Tetrahedron Letters 32, n.º 38 (septiembre de 1991): 5151–52. http://dx.doi.org/10.1016/s0040-4039(00)93452-x.

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4

SAIN, B., S. P. SINGH y J. S. SANDHU. "ChemInform Abstract: Diazabutadienes in Heterocyclic Syntheses: Reaction of 1,3- Diazabutadienes with 2-Oxazolin-5-ones." ChemInform 23, n.º 23 (22 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199223188.

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5

Alvarez-Vald�s, Amparo, Mar�a Jos� Camaz�n, Jos� R. Masaguer y Carmen Navarro-Ranninger. "Complexes of copper(II) with diazabutadienes". Transition Metal Chemistry 12, n.º 1 (febrero de 1987): 55–58. http://dx.doi.org/10.1007/bf01023133.

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6

Bhadbhade, Mohan, Guy K. B. Clentsmith y Leslie D. Field. "Sterically Hindered Diazabutadienes (DABs): Competing Reaction Pathways with MeLi". Organometallics 29, n.º 23 (13 de diciembre de 2010): 6509–17. http://dx.doi.org/10.1021/om100850p.

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7

Nandy Mazumdar, Sujit, Manoj Sharma y Mohinder Pal Mahajan. "Diels-Alder cycloaddition reactions of 1,3-diazabutadienes with sulfene". Tetrahedron Letters 28, n.º 23 (enero de 1987): 2641–42. http://dx.doi.org/10.1016/s0040-4039(00)96169-0.

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8

Mazumdar, Sujit Nandy, Ibrahim Ibnusaud y Mohinder Pal Mahajan. "Diels-alder cycloaddition reactions of 1,3-diazabutadienes with ketenes". Tetrahedron Letters 27, n.º 48 (enero de 1986): 5875–76. http://dx.doi.org/10.1016/s0040-4039(00)85351-4.

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9

Bubnov, Michael P., Vladimir K. Cherkasov, Irina A. Teplova, Nickolay O. Druzhkov, Ivan D. Grishin, Evgenii V. Baranov, Artem S. Bogomyakov y Gleb A. Abakumov. "Novel dioxolene nickel complexes with sterically hindered diazabutadienes. Coupling of aza-ligands coordinated to nickel". Dalton Transactions 48, n.º 28 (2019): 10516–25. http://dx.doi.org/10.1039/c9dt01309a.

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10

Trifonov, Alexander A., Boris G. Shestakov, Konstantin A. Lyssenko, Joulia Larionova, Georgy K. Fukin y Anton V. Cherkasov. "Sterically Governed Redox Reactions. One-Electron Oxidation of Ytterbocenes by Diazabutadienes: Formation of Radical-Anionic Diazabutadiene vs Covalently Bonded Imino–Amido Ligand". Organometallics 30, n.º 18 (26 de septiembre de 2011): 4882–89. http://dx.doi.org/10.1021/om200429h.

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11

Motz, Philip L., John P. Williams, John J. Alexander, Douglas M. Ho, John S. Ricci y Wallace T. Miller. "Coupling of iminoacyl groups to diazabutadienes on manganese carbonyl complexes". Organometallics 8, n.º 6 (junio de 1989): 1523–33. http://dx.doi.org/10.1021/om00108a025.

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12

Morrone, Stefania, Gayle Harrison y Duncan W. Bruce. "Octahedral, liquid-crystalline complexes of 1,4-diazabutadienes with rhenium(I)". Advanced Materials 7, n.º 7 (julio de 1995): 665–67. http://dx.doi.org/10.1002/adma.19950070715.

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13

Diel, Bruce N., Peter J. Deardorff y Catherine M. Zelenski. "Synthesis of new 2,3-perfluoroalkyl- and perfluoroaryl-1,4-diazabutadienes (α-diimines)". Tetrahedron Letters 40, n.º 49 (diciembre de 1999): 8523–27. http://dx.doi.org/10.1016/s0040-4039(99)01692-5.

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14

He, Jing-Yu, Hong-Xing Xin, Hong Yan, Xiu-Qing Song y Ru-Gang Zhong. "Convenient ultrasound-mediated synthesis of 1,4-diazabutadienes under solvent-free conditions". Ultrasonics Sonochemistry 18, n.º 1 (enero de 2011): 466–69. http://dx.doi.org/10.1016/j.ultsonch.2010.08.002.

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15

Dworczak, Renate, Walter M. F. Fabian, Claudia Reidlinger, Alice Rumpler, Jörg Schachner y Klaus Zangger. "Nonlinear optical properties of diazabutadienes and -hexatrienes; experimental and computational aspects". Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy 58, n.º 10 (agosto de 2002): 2135–44. http://dx.doi.org/10.1016/s1386-1425(01)00678-3.

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16

Paparo, Albert, Stephen P. Best, K. Yuvaraj y Cameron Jones. "Neutral, Anionic, and Paramagnetic 1,3,2-Diazaberyllacyles Derived from Reduced 1,4-Diazabutadienes". Organometallics 39, n.º 23 (25 de febrero de 2020): 4208–13. http://dx.doi.org/10.1021/acs.organomet.0c00017.

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17

Avalos, Martín, Reyes Babiano, Pedro Cintas, JoséL Jiménez, Juan C. Palacios y Juan B. Sánchez. "A facile and expeditious entry to acyclic carbohydrate-derived 1,2-diazabutadienes". Tetrahedron: Asymmetry 6, n.º 4 (abril de 1995): 945–56. http://dx.doi.org/10.1016/0957-4166(95)00104-w.

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18

Rojas-Sáenz, Héctor, Galdina V. Suárez-Moreno, Iris Ramos-García, Angélica M. Duarte-Hernández, Edgar Mijangos, Adrián Peña-Hueso, Rosalinda Contreras y Angelina Flores-Parra. "1,4-Dialkyl-1,4-diazabutadienes: their reactions with aluminum and indium halides". New J. Chem. 38, n.º 1 (2014): 391–405. http://dx.doi.org/10.1039/c3nj01226c.

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19

King, Arienne S., Liliya G. Nikolcheva, Christopher R. Graves, Anna Kaminski, Christopher M. Vogels, Robert HE Hudson, Robert J. Ireland, Stephen J. Duffy y Stephen A. Westcott. "Synthesis and reactivity of palladium and platinum diimine complexes containing boronate esters". Canadian Journal of Chemistry 80, n.º 9 (1 de septiembre de 2002): 1217–22. http://dx.doi.org/10.1139/v02-145.

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Condensation of α-diketones (2,3-butanedione, benzil, and acenaphthenequinone) with 3-H2NC6H4Bpin (pin = 1,2-O2C2Me4) gave the corresponding boron-containing α-diimines. The addition of these ligands to [MCl2(coe)]2 (coe = cis-cyclooctene, M = Pd or Pt) gave complexes of the type cis-MCl2(α-diimine) in moderate to high yields. The platinum complexes have been examined for their ability to bind to DNA using enzyme digest studies. These complexes were found to bind to single-stranded DNA as well as, or better than, the non-boron containing controls, and showed binding similar to that of cisplatin (cis-PtCl2(NH3)2).Key words: boronate esters, diazabutadienes, DNA-binding, platinum.
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20

Luthardt, Peter y Ernst-Ulrich Würthwein. "[2+2]- AND [4+2] cycloaddition reactions of 1,3-diazabutadienes with diphenylketene". Tetrahedron Letters 29, n.º 8 (enero de 1988): 921–24. http://dx.doi.org/10.1016/s0040-4039(00)82482-x.

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21

He, Jingyu, Hongxing Xin, Hong Yan, Xiuqing Song y Rugang Zhong. "Synthesis of 1,4-Diazabutadienes (=N,N′-Ethane-1,2-diylidenebis[amines]) by Grinding". Helvetica Chimica Acta 94, n.º 1 (enero de 2011): 159–62. http://dx.doi.org/10.1002/hlca.201000155.

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22

Albert, I. D. L., S. Ramasesha y P. K. Das. "Properties of some low-lying electronic states in polymethineimines and poly(2,3-diazabutadienes)". Physical Review B 43, n.º 9 (15 de marzo de 1991): 7013–19. http://dx.doi.org/10.1103/physrevb.43.7013.

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23

AVALOS, M., R. BABIANO, P. CINTAS, J. L. JIMENEZ, J. C. PALACIOS y J. B. SANCHEZ. "ChemInform Abstract: A Facile and Expeditious Entry to Acyclic Carbohydrate-Derived 1,2- Diazabutadienes." ChemInform 26, n.º 36 (17 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199536242.

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24

Rojas-Saenz, Hector, Galdina V. Suarez-Moreno, Iris Ramos-Garcia, Angelica M. Duarte-Hernandez, Edgar Mijangos, Adrian Pena-Hueso, Rosalinda Contreras y Angelina Flores-Parra. "ChemInform Abstract: 1,4-Dialkyl-1,4-diazabutadienes: Their Reactions with Aluminum and Indium Halides." ChemInform 45, n.º 20 (28 de abril de 2014): no. http://dx.doi.org/10.1002/chin.201420111.

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25

Diel, Bruce N., Peter J. Deardorff y Catherine M. Zelenski. "ChemInform Abstract: Synthesis of New 2,3-Perfluoroalkyl- and Perfluoroaryl-1,4-diazabutadienes (α-Diimines)". ChemInform 31, n.º 9 (10 de junio de 2010): no. http://dx.doi.org/10.1002/chin.200009078.

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26

Barluenga, José, Miguel Tomás, Alfredo Ballesteros y Luis A. López. "1,4-Cycloaddition of 1,3-diazabutadienes with enamines: An efficient route to the pyrimidine ring". Tetrahedron Letters 30, n.º 34 (enero de 1989): 4573–76. http://dx.doi.org/10.1016/s0040-4039(01)80748-6.

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27

Booth, Corwin H., Marc D. Walter, Daniel Kazhdan, Yung-Jin Hu, Wayne W. Lukens, Eric D. Bauer, Laurent Maron, Odile Eisenstein y Richard A. Andersen. "Decamethylytterbocene Complexes of Bipyridines and Diazabutadienes: Multiconfigurational Ground States and Open-Shell Singlet Formation". Journal of the American Chemical Society 131, n.º 18 (13 de mayo de 2009): 6480–91. http://dx.doi.org/10.1021/ja809624w.

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28

He, Jingyu, Hongxing Xin, Hong Yan, Xiuqing Song y Rugang Zhong. "ChemInform Abstract: Synthesis of 1,4-Diazabutadienes (=N,N′-Ethane-1,2-diylidenebis[amines]) by Grinding." ChemInform 42, n.º 17 (31 de marzo de 2011): no. http://dx.doi.org/10.1002/chin.201117055.

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29

Faust, Rüdiger, Bernd Göbelt y Christian Weber. "Triisopropylsilyl Protected Hexa-1,5-diyne-3,4-dione: A Convenient Precursor to 2,3-Dialkynyl 1,4-Diazabutadienes". Synlett 1998, n.º 01 (enero de 1998): 64–66. http://dx.doi.org/10.1055/s-1998-1559.

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30

Faust, Rüdiger y Bernd Göbelt. "First 2,3-Dialkynyl-1,4-diazabutadienes by Pd-Catalyzed Cross-Coupling of Bis(imidoyl chlorides) and Alkynylstannanes". Tetrahedron Letters 38, n.º 46 (noviembre de 1997): 8017–20. http://dx.doi.org/10.1016/s0040-4039(97)10218-0.

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31

Janich, Simon, Roland Fröhlich, Andrea Wilken, Jan von Zamory, Atsushi Wakamiya, Shigehiro Yamaguchi y Ernst-Ulrich Würthwein. "3,4-Dihydro-3H-pyrrol-2-imines as Conformationally Restrained 1,3-Diazabutadienes: Synthesis, Structural Properties and Protonation". European Journal of Organic Chemistry 2009, n.º 13 (mayo de 2009): 2077–87. http://dx.doi.org/10.1002/ejoc.200900045.

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32

Imhof, Wolfgang y Ernst Anders. "Regioselectivity in Iron-Catalyzed [2+2+1] Cycloadditions: A DFT Investigation of Substituent Effects in 1,4-Diazabutadienes". Chemistry - A European Journal 10, n.º 22 (19 de noviembre de 2004): 5717–29. http://dx.doi.org/10.1002/chem.200400215.

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33

FAUST, R., B. GOEBELT y C. WEBER. "ChemInform Abstract: Triisopropylsilyl Protected Hexa-1,5-diyne-3,4-dione: A Convenient Precursor to 2,3-Dialkynyl 1,4-Diazabutadienes." ChemInform 29, n.º 17 (23 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199817087.

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34

Bootz, Konrad y Wilhelm P. Neumann. "The first synthesis of aza-germacyclopentenes: Cycloadditions of 1-aza- and 1,4-diazabutadienes with free singlet dimethyl germylene". Tetrahedron Letters 30, n.º 48 (1989): 6669–72. http://dx.doi.org/10.1016/s0040-4039(00)70646-0.

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35

FAUST, R. y B. GOEBELT. "ChemInform Abstract: First 2,3-Dialkynyl-1,4-diazabutadienes by Pd-Catalyzed Cross-Coupling of Bis(imidoyl chlorides) and Alkynylstannanes." ChemInform 29, n.º 7 (24 de junio de 2010): no. http://dx.doi.org/10.1002/chin.199807041.

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36

Singh, G. S. y K. Kopo. "ChemInform Abstract: Synthesis of 1,1,4,4-Tetraryl-1,3-diazabutadienes (II) by Oxidation of Hydrazones (I) Using Bis(acetylacetonato)copper(II)." ChemInform 33, n.º 46 (19 de mayo de 2010): no. http://dx.doi.org/10.1002/chin.200246113.

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37

Barluenga, José, Miguel Tomás, Alfredo Ballesteros y Luis A. López. "A Simple, Regioselective Synthesis of 5,6-Dihydro-1,3,5-triazine-2,4(1H,3H)-dione Derivatives fromN-Trimethylsilyl Imines via 1,3-Diazabutadienes". Synthesis 1989, n.º 03 (1989): 228–29. http://dx.doi.org/10.1055/s-1989-27212.

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38

Baker, Robert J., Robert D. Farley, Cameron Jones, Marc Kloth y Damien M. Murphy. "The reactivity of diazabutadienes toward low oxidation state Group 13 iodides and the synthesis of a new gallium(i) carbene analogue". Journal of the Chemical Society, Dalton Transactions, n.º 20 (2002): 3844. http://dx.doi.org/10.1039/b206605j.

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39

Das, Samir, Indranil Chakraborty y Animesh Chakravorty. "Rhenium Chemistry of Diazabutadienes and Derived Iminoacetamides Spanning the Valence Domain II−VI. Synthesis, Characterization, and Metal-Promoted Regiospecific Imine Oxidation". Inorganic Chemistry 42, n.º 20 (octubre de 2003): 6545–55. http://dx.doi.org/10.1021/ic034586c.

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40

Kia, Reza y Azadeh Kalaghchi. "Intra- and intermolecular interactions in a series of chlorido-tricarbonyl-diazabutadienerhenium(I) complexes: structural and theoretical studies". Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 76, n.º 3 (16 de mayo de 2020): 417–26. http://dx.doi.org/10.1107/s2052520620004333.

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A series of new chlorido-tricarbonylrhenium(I) complexes bearing alkyl-substituted diazabutadiene (DAB) ligands, namely N,N′-bis(2,4-dimethylbenzene)-1,4-diazabutadiene (L1), N,N′-bis(2,4-dimethylbenzene)-2,3-dimethyl-1,4-diazabutadiene (L2), N,N′-bis(2,4,6-trimethylbenzene)-2,3-dimethyl-1,4-diazabutadiene (L3) and N,N′-bis(2,6-diisopropylbenzene)-1,4-diazabutadiene (L4), were synthesized and investigated. The crystal structures have been fully characterized by X-ray diffraction and spectroscopic methods. Density functional theory, natural bond orbital and non-covalent interaction index methods have been used to study the optimized geometry in the gas phase and intra- and intermolecular interactions in the complexes, respectively. The most important studied interactions in these metal carbonyl complexes are n→π*, n→σ* and π→π*. Among complexes 1–4, only 2 shows interesting intermolecular n→π* interactions due to lp(C[triple-bond]O)...π* and lp(Cl)...π* (lp = lone pair) contacts.
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41

Kia, Reza y Azadeh Kalaghchi. "Structural, Non-Covalent Interaction, and Natural Bond Orbital Studies on Bromido-Tricarbonyl Rhenium(I) Complexes Bearing Alkyl-Substituted 1,4-Diazabutadiene (DAB) Ligands". Crystals 10, n.º 4 (1 de abril de 2020): 267. http://dx.doi.org/10.3390/cryst10040267.

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The synthesis, characterization, structural and computational studies of Re(I) tricarbonyl bromo complexes bearing alkyl-substituted 1,4-diazabutadiene ligands, [Re(CO)3(1,4-DAB)Br], where 1,4-DAB = N,N-bis(2,4-dimethylbenzene)-1,4-diazabutadiene, 2,4-Me2DAB (1); N,N-bis(2,4-dimethylbenzene)-2,3-dimethyl-1,4-diazabutadiene, 2,4-Me2DABMe (2); N,N-bis(2,4,6-trimethylbenzene)-1,4-diazabutadiene, 2,4,6-Me3DAB (3); and N,N-bis(2,6-diisopropylbenzene)-1,4-diazabutadiene, 2,6-ipr2DAB (4) are reported. The complexes were characterized by different spectroscopic methods such as FT-IR, 1H-NMR, 13C-NMR, and elemental analyses and their solid-state structures were confirmed by X-ray diffraction. In each complex, the Re(I) centre shows a distorted octahedral shape with a facial geometry of carbonyl groups. The gas phase geometry of the complexes was identified by density functional theory. Interesting intermolecular n…π* interactions of complexes 1 and 3 were investigated by non-covalent interaction index (NCI), and natural bond orbital (NBO) analyses. The intramolecular n…σ*, σ…π*, π…σ* interactions were also studied in complexes 3 and 4.
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42

Zhao, Jie, Jianchao Yuan, Weibing Xu, Jingjing Chen y Yanqiong Mu. "2,3-Bis{[2,3-dimethyl-6-(phenylvinyl)phenyl]imino}butane". Acta Crystallographica Section E Structure Reports Online 70, n.º 2 (11 de enero de 2014): o130. http://dx.doi.org/10.1107/s1600536814000440.

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In the title compound, C36H36N2, a product of the condensation reaction of 2,3-dimethyl-6-phenylvinylbenzenamine and 2,3-butanedione, the complete molecule is generated by the application of an inversion centre. The central C—C bond in the 1,4-diazabutadiene fragment istrans-configured and situated about the inversion center. The dihedral angle between the ring attached to N and the 1,4-diazabutadiene plane is 78.24 (36)°, while the 1,4-diazabutadiene plane makes an angle of 30.71 (26)° with the phenyl ring.
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43

Pott, Thomas, Peter Jutzi, Beate Neumann y Hans-Georg Stammler. "Differing Reactivities of Cp*Ga toward Diazabutadienes: Synthesis of Novel 1-Galla-2,5-diazoles and of the Known Radical Ga[But-DAB]2". Organometallics 20, n.º 10 (mayo de 2001): 1965–67. http://dx.doi.org/10.1021/om001045b.

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44

Sain, Bir, Satyendra P. Singh y Jagir S. Sandhu. "Diazabutadienes in heterocyclic syntheses. Preparation of pyrimidin-6-ones by reaction of 4-dialkylamino-1,3-diaza-1,3-butadienes with 2-oxazolin-5-ones". Tetrahedron 48, n.º 22 (enero de 1992): 4567–78. http://dx.doi.org/10.1016/s0040-4020(01)81230-8.

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45

Weber, Lothar, Jan Förster, Hans-Georg Stammler y Beate Neumann. "Contribution to the Reactivity ofN,N′-Diaryl-1,4-diazabutadienes Aryl–N=CH–CH=N–Aryl (Aryl = 2,6-Dimethylphenyl; 2,4,6-Trimethylphenyl) Towards Boron Trichloride". European Journal of Inorganic Chemistry 2006, n.º 24 (diciembre de 2006): 5048–56. http://dx.doi.org/10.1002/ejic.200600728.

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Lv, Wen-Xian, Jian Li, Yu-Lai Hu, Ying-Peng Su y Dan-Feng Huang. "(Z)-N-[(Z)-3-(2,5-Dimethylphenylimino)butan-2-ylidene]-2,5-dimethylaniline". Acta Crystallographica Section E Structure Reports Online 70, n.º 2 (22 de enero de 2014): o175. http://dx.doi.org/10.1107/s1600536814001020.

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The asymmetric unit of the title compound, C20H24N2, contains one half-molecule, with the single C—C bond of the 1,4-diazabutadiene fragment situated on a centre of symmetry. The benzene rings are inclined to the 1,4-diazabutadiene mean plane by 59.5 (1)°.
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Uhl, Werner, Jens Molter y Bernhard Neumüller. "Synthesis of Aluminum Hydrazides by Hydroalumination of 2,3-Diazabutadienes—Formation of an Al4(N2)3 Cage Compound and an Al3(N2)3 Macrocyclic Ligand". Chemistry 7, n.º 7 (1 de abril de 2001): 1510–15. http://dx.doi.org/10.1002/1521-3765(20010401)7:7<1510::aid-chem1510>3.0.co;2-p.

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SAIN, B., S. P. SINGH y J. S. SANDHU. "ChemInform Abstract: Diazabutadienes in Heterocyclic Syntheses. Preparation of Pyrimidin-6- ones by Reaction of 4-Dialkylamino-1,3-diaza-1,3-butadienes with 2- Oxazolin-5-ones." ChemInform 23, n.º 39 (21 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199239208.

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Trifonov, Alexander A., Elena A. Fedorova, Georgy K. Fukin, Evgenii V. Baranov, Nikolai O. Druzhkov y Mikhail N. Bochkarev. "Bridging μ-η5:η4-Coordination of an Indenyl Ligand and Reductive Coupling of Diazabutadienes in the Assembly of Di- and Tetranuclear Mixed-Valent Ytterbium Indenyldiazabutadiene Complexes". Chemistry - A European Journal 12, n.º 10 (20 de marzo de 2006): 2752–57. http://dx.doi.org/10.1002/chem.200501181.

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WEIDENBRUCH, M., A. LESCH y K. PETERS. "ChemInform Abstract: Silicon Compounds with Strongly Intramolecular Steric Interactions. Part 44. (4 +1) Versus (4 + 2) Cycloaddition of Di-tert.-butylsilylene and Tetra-tert.-butyldisilene to 1,4-Diazabutadienes." ChemInform 22, n.º 26 (23 de agosto de 2010): no. http://dx.doi.org/10.1002/chin.199126221.

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