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Journal articles on the topic 'Alkine'

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Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Zulys, Agustino, Maximilian Dochnahl, Dirk Hollmann, Karolin Löhnwitz, Jost-Steffen Herrmann, Peter W. Roesky, and Siegfried Blechert. "Intramolekulare Hydroaminierung funktionalisierter Alkene und Alkine mit einem Zink-Homogenkatalysator." Angewandte Chemie 117, no. 47 (December 2, 2005): 7972–76. http://dx.doi.org/10.1002/ange.200502006.

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2

Haberlag, Birte, Matthias Freytag, Constantin G. Daniliuc, Peter G. Jones, and Matthias Tamm. "Effiziente Metathese terminaler Alkine." Angewandte Chemie 124, no. 52 (November 14, 2012): 13195–99. http://dx.doi.org/10.1002/ange.201207772.

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3

Tillack, Annegret, Ivette Garcia Castro, Christian G. Hartung, and Matthias Beller. "Anti-Markownikow-Hydroaminierung terminaler Alkine." Angewandte Chemie 114, no. 14 (July 15, 2002): 2646–48. http://dx.doi.org/10.1002/1521-3757(20020715)114:14<2646::aid-ange2646>3.0.co;2-a.

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4

Sükel, Karlheinz. "Komplexchemie perhalogenierter Cyclopentadiene und Alkine." Journal of Organometallic Chemistry 348, no. 1 (June 1988): C12—C14. http://dx.doi.org/10.1016/0022-328x(88)80350-4.

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5

Sünkel, Karlheinz, and Doris Steiner. "Komplexchemie perhalogenierter Cyclopentadiene und Alkine." Journal of Organometallic Chemistry 368, no. 1 (May 1989): 67–76. http://dx.doi.org/10.1016/0022-328x(89)80119-6.

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6

Sünkel, Karlheinz. "Komplexchemie perhalogenierter cyclopentadiene und alkine." Journal of Organometallic Chemistry 436, no. 1 (September 1992): 101–8. http://dx.doi.org/10.1016/0022-328x(92)85031-q.

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7

Sünkel, Karlheinz, and Uwe Birk. "Komplexchemie perhalogenierter cyclopentadiene und alkine." Journal of Organometallic Chemistry 458, no. 1-2 (October 1993): 181–86. http://dx.doi.org/10.1016/0022-328x(93)80471-m.

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8

Freitag, Sarah, Jens Henning, Hartmut Schubert, and Lars Wesemann. "Phosphastanniran: Ein Phosphor/Zinn(II)-Lewis-Paar, das Alkine und Alkene addiert." Angewandte Chemie 125, no. 21 (April 15, 2013): 5750–54. http://dx.doi.org/10.1002/ange.201301153.

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9

Haas, Alois, and Hans-Udo Krächter. "Darstellung und Reaktionen Trifluormethylchalkogenyl-substituierter Alkine." Chemische Berichte 121, no. 10 (October 1988): 1833–40. http://dx.doi.org/10.1002/cber.19881211023.

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10

Neumann, Wilhelm P., Hideki Sakurai, Gilbert Billeb, Hartmut Brauer, Jürgen Köcher, and Sabine Viebahn. "Addition von freiem Me2Ge: An Alkene und Alkine in Gegenwart von Wasser auf Glasoberflächen." Angewandte Chemie 101, no. 8 (January 13, 2006): 1074–76. http://dx.doi.org/10.1002/ange.19891010829.

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11

Brenzovich, William E. "Gold in der Totalsynthese: Alkine als Carbonylersatz." Angewandte Chemie 124, no. 36 (July 13, 2012): 9063–65. http://dx.doi.org/10.1002/ange.201204598.

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12

Wang, Xing Qiang. "The Effects of Composite Enzymes in Diets on Growth, Carcass Composition and Specific Enzyme Activities of Juvenile Paralichthys lethostigma." Advanced Materials Research 518-523 (May 2012): 5493–99. http://dx.doi.org/10.4028/www.scientific.net/amr.518-523.5493.

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The study was conducted to investigate the effects of commercial composite enzymes (CE) on growth, carcass composition and specific enzyme activities of juvenile flounder Paralichthys lethostigma. Four diets were formulated: one diet contained no CE (the control), the three others provided graded levels of CE (0.5%, 1% and 1.5%). Each diet was fed to pentaplicate of flounder juveniles for 28 days in aquaria (50×40×30 cm, water volume 50 L). The growth parameters (final wet weight, specific growth rate: SGR, feed conversion rate: FCR and apparent digestibility: AD) were significantly affected (P0.05). The CE had significant effects (P<0.05) on the specific activities of neural protease, alkine protease and amylase, but not on acid protease, amimopeptidase and alkine phosphatase. The pattern of the specific activities of neural protease, alkine protease and amylase was similar to that of SGR with fish fed diets containing 1.5% of CE exhibited the significantly higher activities (P<0.05). The results demonstrated that the supplement of CE in diets could significantly improve growth performance and digestive enzyme activities of flounder juveniles.

13

Lehrich, Friedhelm, and Henning Hopf. "Alkine und cumulene, XIX: Kreuzkonjugierte mono- und diallene." Tetrahedron Letters 28, no. 24 (January 1987): 2697–700. http://dx.doi.org/10.1016/s0040-4039(00)96184-7.

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14

Haberlag, Birte, Matthias Freytag, Constantin G. Daniliuc, Peter G. Jones, and Matthias Tamm. "Innentitelbild: Effiziente Metathese terminaler Alkine (Angew. Chem. 52/2012)." Angewandte Chemie 124, no. 52 (November 28, 2012): 13074. http://dx.doi.org/10.1002/ange.201208969.

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15

Shi, Shuai, Tao Wang, Vanessa Weingand, Matthias Rudolph, and A. Stephen K. Hashmi. "Gold(I)-katalysierte diastereoselektive Hydroacylierung terminaler Alkine mit Glyoxalen." Angewandte Chemie 126, no. 4 (December 11, 2013): 1166–70. http://dx.doi.org/10.1002/ange.201307685.

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16

Lang, Heinrich, and Uwe Lay. "Stereoselektive additionsreaktionen von komplexgebundenen phosphanen und arsanen an alkine." Journal of Organometallic Chemistry 441, no. 3 (December 1992): 389–96. http://dx.doi.org/10.1016/0022-328x(92)80170-3.

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17

Giuffrè, Angelo Maria. "n-Alkanes and n-Alkenes in Virgin Olive Oil from Calabria (South Italy): The Effects of Cultivar and Harvest Date." Foods 10, no. 2 (February 1, 2021): 290. http://dx.doi.org/10.3390/foods10020290.

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n-Alkanes and n-alkenes are components of the unsaponifiable fraction of an olive oil. These were analysed by GC on-column analysis and are here proposed as an additional tool to certify the origin, authenticity, traceability and chemical quality of olive oil produced in the Reggio Calabria province (South Italy). Nine cultivars were studied: Cassanese, Coratina, Itrana, Leccino, Nociara, Ottobratica, Pendolino, Picholine and Sinopolese grown in the region of Calabria (South Italy). n-Alkanes in the range from 21 to 35 chain carbon atoms and alkenes in the range from 23:1 to 25:1 chain carbon atoms were found with the following elution order: heneicosane (C21), docosane (C22), tricosene (C23:1), tricosane (C23), tetracosene (C24:1), tetracosane (C24), pentacosene (C25:1), pentacosane (C25), hexacosane (C26), eptacosane (C27), octacosane (C28), nonacosane (C29), triacontane (C30), entriacontane (C31), dotriacontane (C32), tritriacontane (C33), tetratriacontane (C34), pentatriacontane (C35). The oil of all cultivars showed a decreasing trend in total n-alkane and n-alkene content, with the oil of Sinopolese showing the highest content, varying from 328.50 to 214.00 mg/kg. Odd-chain alkanes predominated over even-chain n-alkanes, and tricosane, tetracosane and pentacosane were the most represented alkanes. Cultivar and harvest date significantly influenced the n-alkane and n-alkene content. These findings can be useful to distinguish different olive cultivars and to decide the fruit harvest date for the oil of the Reggio Calabria province (South Italy). A daily quantity of 30 g of olive oil of the Sinoplese cv (the one with the highest n-alkane and n-alkene content) was found to be in accordance with the suggestions of the European Agency for the evaluation of medicinal products Committee for veterinary medicinal products and biogenic hydrocarbons intake for the human diet.

18

Hopf, Henning, Olaf Kretschmer, and Ludger Ernstb. "Alkine und Cumulene, XXI. über einige neue Oligomere des Allens." Chemische Berichte 123, no. 5 (May 1990): 1169–74. http://dx.doi.org/10.1002/cber.19901230534.

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19

Pawliczek, Martin, Tobias F. Schneider, Christian Maaß, Dietmar Stalke, and Daniel B. Werz. "Formaleanti-Carbopalladierungen nicht-aktivierter Alkine: Voraussetzungen, mechanistische Untersuchungen und Anwendungen." Angewandte Chemie 127, no. 13 (February 4, 2015): 4192–96. http://dx.doi.org/10.1002/ange.201411210.

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20

Johnson, John R., Gregory D. Cuny, and Stephen L. Buchwald. "Rhodium-katalysierte Hydroformylierung innerer Alkine zu α,β-ungesättigten Aldehyden." Angewandte Chemie 107, no. 16 (August 18, 1995): 1877–79. http://dx.doi.org/10.1002/ange.19951071613.

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21

Doyle, Michael P., Doina G. Ene, Chad S. Peterson, and Vince Lynch. "Makrocyclische Cyclopropene durch hochenantioselektive intramolekulare Additionen von Metallcarbenen an Alkine." Angewandte Chemie 111, no. 5 (March 1, 1999): 722–24. http://dx.doi.org/10.1002/(sici)1521-3757(19990301)111:5<722::aid-ange722>3.0.co;2-r.

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22

Hua, Huiming, Tao Yuan, Yeling Wang, and Yuehu Pei. "A new aromatic alkine from the tuber of Sparganium stoloniferum." Fitoterapia 78, no. 3 (April 2007): 274–75. http://dx.doi.org/10.1016/j.fitote.2006.11.014.

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23

Gotthardt, Hans, Hans-Georg Kinzelmann, Ulrich Feist, and Joachim Buddrus. "Zur Regio- und Stereoselektivität neuer thermischer [3 + 2]-Cycloadditionen mesoionischer 1,3-Oxathiol-4-one an Alkine und Alkene." Chemische Berichte 119, no. 7 (July 1986): 2317–38. http://dx.doi.org/10.1002/cber.19861190723.

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24

Hopf, Henning, and Elke Naujoks. "Alkine und cumulene-XX. Trimethylsilylallene durch retro-en-spaltung von trimethylsilylpropargylethern." Tetrahedron Letters 29, no. 6 (1988): 609–10. http://dx.doi.org/10.1016/s0040-4039(00)80162-8.

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25

Siegel, Herbert, Ludwig Eisenhuth, and Henning Hopf. "Alkine und Cumulene, XVII. Photoadditionen von Vinylacetylen an andere ungesättigte Kohlenwasserstoffe." Chemische Berichte 118, no. 2 (February 1985): 597–612. http://dx.doi.org/10.1002/cber.19851180219.

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26

Hopf, Henning, Ludwig Eisenhuth, Verena Lehne, and Ludger Ernst. "Alkine und Cumulene, XVIII. Zur Acetylen-Oligomerisierung nachNieuwland: Struktur der Tetrameren." Chemische Berichte 119, no. 3 (March 1986): 1105–9. http://dx.doi.org/10.1002/cber.19861190332.

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27

Hopf, Henning, Olaf Kretschmer, Ludger Ernst, and Ludger Witte. "Alkine und Cumulene, XXII. Die thermische Di- und Trimerisierung vontert-Butylallen." Chemische Berichte 124, no. 4 (April 1991): 875–79. http://dx.doi.org/10.1002/cber.19911240430.

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28

Xiao, Jian, and Xingwei Li. "Gold-α-Oxocarbenoide in der katalysierten Übertragung von Sauerstoffatomen auf Alkine." Angewandte Chemie 123, no. 32 (July 1, 2011): 7364–75. http://dx.doi.org/10.1002/ange.201100148.

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29

Haydl, Alexander M., Bernhard Breit, Tao Liang, and Michael J. Krische. "Alkine als alternativer Einstieg in elektrophile und nukleophile Übergangsmetall-katalysierte Allylierungen." Angewandte Chemie 129, no. 38 (August 10, 2017): 11466–80. http://dx.doi.org/10.1002/ange.201704248.

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30

Dove, H., and M. Oliván. "The possible use of the alkenes (unsaturated hydrocarbons) of plant cuticular wax as diet composition markers in sheep." BSAP Occasional Publication 34 (2006): 1–7. http://dx.doi.org/10.1017/s1463981500042187.

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SummaryThe objective of the current study was to investigate the possible use of alkenes (unsaturated hydrocarbons) of plant waxes as diet composition markers in sheep. Twenty-four sheep (30 kg live weight) were housed in individual pens (n=16, “pen” sheep) or in metabolism crates (n=8, “crate” sheep) for the total collection of faeces. Once daily, sheep were fed 720 g DM of a two-component diet consisting of a roughage source (chaffed perennial ryegrass) and a high-quality supplement (unpelleted sunflower meal, SFM) in different proportions, 7:1, 6:2, 5:3 and 4:4 (4 pen sheep and 2 crate sheep/treatment). SFM was labelled with a solution of beeswax to provide an alkane/ alkene profile different from the chaff. Diet composition was estimated from C27, C29, C31 and C33 alkene concentrations in diet and faeces (total faeces or rectal grab samples), using the least-squares package ‘EatWhat’. Estimates were conducted with or without correction of faecal alkane concentrations for incomplete faecal recovery, calculated from the alkene intakes and faecal outputs in the crate sheep.Although the faecal alkene recoveries of alkenes were low, they did not differ between chain lengths for alkenes C27 to C33. Therefore in cage sheep, alkene-based estimates of SFM proportions, with or without faecal recovery correction, did not differ significantly from the proportions fed and were as accurate as earlier alkane-based estimates. In pen sheep, SFM proportions estimated from rectal grab samples were slightly but significantly over-estimated, regardless of whether or not recovery corrections were used. The over-estimates were not related to recovery corrections but to the small differences in concentrations between rectal grab samples from pen sheep and the total faeces from cage sheep. The lack of effect of recovery corrections does not mean they should be excluded from such calculations, as there may be situations in which there is an effect of carbon-chain length on alkene recovery. Use of recovery corrections also permits an estimate of whole-diet digestibility.The present results indicate that alkenes could be useful additional markers to the alkanes for estimating the proportion of two dietary components in diets offered to sheep.

31

Maercker, Adalbert, Thomas Graule, and Ulrich Girreser. "Vicinale Dilithioalkene durch Addition von Lithium an einfache cyclische und acyclische Alkine." Angewandte Chemie 98, no. 2 (February 1986): 174–76. http://dx.doi.org/10.1002/ange.19860980214.

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32

Giese, Bernd, and Stephen Lachhein. "Addition von Alkyl-Radikalen an Alkine: Unterscheidung zwischen radikalischer und ionischer Nucleophilie." Angewandte Chemie 94, no. 10 (January 19, 2006): 780–81. http://dx.doi.org/10.1002/ange.19820941006.

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33

Liu, Yuanhong, Baojian Shen, Martin Kotora, and Tamotsu Takahashi. "Inter- und intramolekulare Carbometallierung nichtaktivierter Alkine durch Zirconacyclopentane in Gegenwart von Kupferchlorid." Angewandte Chemie 111, no. 7 (April 1, 1999): 966–68. http://dx.doi.org/10.1002/(sici)1521-3757(19990401)111:7<966::aid-ange966>3.0.co;2-l.

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34

FELL, Bernhard, and Hans-Henning VOGEL. "Synthese von β, γ-ungesättigten Carbonsäuren durch Radikal-Addition an Δ1-Alkine." Synthesis 1969, no. 02 (September 19, 2002): 76–77. http://dx.doi.org/10.1055/s-1969-20378.

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35

Grossi, Vincent, Cristiana Cravo-Laureau, Alain Méou, Danielle Raphel, Frédéric Garzino, and Agnès Hirschler-Réa. "Anaerobic 1-Alkene Metabolism by the Alkane- and Alkene-Degrading Sulfate Reducer Desulfatibacillum aliphaticivorans Strain CV2803T." Applied and Environmental Microbiology 73, no. 24 (October 26, 2007): 7882–90. http://dx.doi.org/10.1128/aem.01097-07.

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ABSTRACT The alkane- and alkene-degrading, marine sulfate-reducing bacterium Desulfatibacillum aliphaticivorans strain CV2803T, known to oxidize n-alkanes anaerobically by fumarate addition at C-2, was investigated for its 1-alkene metabolism. The total cellular fatty acids of this strain were predominantly C-(even number) (C-even) when it was grown on C-even 1-alkenes and predominantly C-(odd number) (C-odd) when it was grown on C-odd 1-alkenes. Detailed analyses of those fatty acids by gas chromatography-mass spectrometry after 6- to 10-week incubations allowed the identification of saturated 2- and 4-ethyl-, 2- and 4-methyl-, and monounsaturated 4-methyl-branched fatty acids with chain lengths that correlated with those of the 1-alkene. The growth of D. aliphaticivorans on (per)deuterated 1-alkenes provided direct evidence of the anaerobic transformation of these alkenes into the corresponding 1-alcohols and into linear as well as 10- and 4-methyl-branched fatty acids. Experiments performed with [13C]bicarbonate indicated that the initial activation of 1-alkene by the addition of inorganic carbon does not occur. These results demonstrate that D. aliphaticivorans metabolizes 1-alkene by the oxidation of the double bond at C-1 and by the subterminal addition of organic carbon at both ends of the molecule [C-2 and C-(ω-1)]. The detection of ethyl-branched fatty acids from unlabeled 1-alkenes further suggests that carbon addition also occurs at C-3. Alkylsuccinates were not observed as potential initial intermediates in alkene metabolism. Based on our observations, the first pathways for anaerobic 1-alkene metabolism in an anaerobic bacterium are proposed. Those pathways indicate that diverse initial reactions of 1-alkene activation can occur simultaneously in the same strain of sulfate-reducing bacterium.

36

Teles, J. Henrique, Stefan Brode, and Mathieu Chabanas. "Kationische Gold(I)-Komplexe: hocheffiziente Katalysatoren für die Addition von Alkoholen an Alkine." Angewandte Chemie 110, no. 10 (May 18, 1998): 1475–78. http://dx.doi.org/10.1002/(sici)1521-3757(19980518)110:10<1475::aid-ange1475>3.0.co;2-l.

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37

Breuer, Klaus, J. Henrique Teles, Dirk Demuth, Hartmut Hibst, Ansgar Schäfer, Stefan Brode, and Hilde Domgörgen. "Zinksilicate: hochwirksame heterogene Katalysatoren für die Addition primärer Alkohole an Alkine und Allene." Angewandte Chemie 111, no. 10 (May 17, 1999): 1497–502. http://dx.doi.org/10.1002/(sici)1521-3757(19990517)111:10<1497::aid-ange1497>3.0.co;2-2.

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38

Tokunaga, Makoto, Markus Eckert, and Yasuo Wakatsuki. "Rutheniumkatalysierte intermolekulare Hydroaminierung terminaler Alkine mit Anilinen: eine praktikable Synthese von aromatischen Ketiminen." Angewandte Chemie 111, no. 21 (November 2, 1999): 3416–19. http://dx.doi.org/10.1002/(sici)1521-3757(19991102)111:21<3416::aid-ange3416>3.0.co;2-6.

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39

Potapov, Vladimir A., Maxim V. Musalov, Evgeny O. Kurkutov, Vladimir A. Yakimov, Alfiya G. Khabibulina, Maria V. Musalova, Svetlana V. Amosova, Tatyana N. Borodina, and Alexander I. Albanov. "Remarkable Alkene-to-Alkene and Alkene-to-Alkyne Transfer Reactions of Selenium Dibromide and PhSeBr. Stereoselective Addition of Selenium Dihalides to Cycloalkenes." Molecules 25, no. 1 (January 3, 2020): 194. http://dx.doi.org/10.3390/molecules25010194.

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The original goal of this research was to study stereochemistry of selenium dihalides addition to cycloalkenes and properties of obtained products. Remarkable alkene-to-alkene and alkene-to-alkyne transfer reactions of selenium dibromide and PhSeBr were discovered during this research. The adducts of selenium dibromide with alkenes or cycloalkenes easily exchange SeBr2 with other unsaturated compounds, including acetylenes, at room temperature, in acetonitrile. Similar alkene-to-alkene and alkene-to-alkyne transfer reactions of the PhSeBr adducts with alkenes or cycloalkenes take place. The supposed reaction pathway includes the selenium group transfer from seleniranium species to alkenes or alkynes. It was found that the efficient SeBr2 and PhSeBr transfer reagents are Se(CH2CH2Br)2 and PhSeCH2CH2Br, which liberate ethylene, leading to a shift in equilibrium. The regioselective and stereoselective synthesis of bis(E-2-bromovinyl) selenides and unsymmetrical E-2-bromovinyl selenides was developed based on the SeBr2 and PhSeBr transfer reactions which proceeded with higher selectivity compared to analogous addition reactions of SeBr2 and PhSeBr to alkynes under the same conditions.

40

Choi, Seung S., M. Y. Jung, C. K. Chun, J. W. Kim, J. H. Boo, and J. S. Yang. "Nanofabrication of NSOM Probe on the Cantilever Array." International Journal of Nanoscience 02, no. 01n02 (February 2003): 65–73. http://dx.doi.org/10.1142/s0219581x03001012.

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In this paper, a new process to fabricate nanosized silicon oxide apertures on a cantilever array is presented. The various semiconductor processes such as alkine etching, stress-dependent thermal oxidation, dilute HF etching and Au sputter deposition were utilized. With the dilute HF etching process, the opening of the nanosized oxide aperture could be fabricated in a controlled manner. The Au thin layer was deposited on the oxide apertures on the cantilever array so that the 160 nm apertures on a (5×1) cantilever array were successfully fabricated.

41

Kim, Hyung Min, Dong Sung Kim, Yong Joo Sung, Young Seok Park, and Yong-Gyo Seo. "Study of the Precipitation of Silica from Black Liquor of Rice Husk Alkine Digestion." Journal of Korea Technical Association of the Pulp and Paper Industry 49, no. 4 (August 31, 2017): 143–49. http://dx.doi.org/10.7584/jktappi.2017.08.49.4.143.

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42

Kong, Xiangbin, Ning Wang, Qixing Zhang, Junhui Liang, Manjing Wang, Changchun Wei, Xinliang Chen, Ying Zhao, and Xiaodan Zhang. "Ni-Doped MoS2 as an Efficient Catalyst for Electrochemical Hydrogen Evolution in Alkine Media." ChemistrySelect 3, no. 32 (August 30, 2018): 9493–98. http://dx.doi.org/10.1002/slct.201802100.

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43

Tokunaga, Makoto, and Yasuo Wakatsuki. "Die erste Anti-Markownikow-Hydratisierung terminaler Alkine: Ruthenium(II)/ Phosphan-katalysierte Bildung von Aldehyden." Angewandte Chemie 110, no. 20 (October 16, 1998): 3024–27. http://dx.doi.org/10.1002/(sici)1521-3757(19981016)110:20<3024::aid-ange3024>3.0.co;2-0.

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44

Neisius, N. Matthias, and Bernd Plietker. "Die Ruthenium-katalysierte Hydrovinylierung interner Alkine mit Acrylsäurederivaten - ein atomökonomischer Zugang zu hochsubstituierten 1,3-Dienen." Angewandte Chemie 121, no. 31 (July 20, 2009): 5863–66. http://dx.doi.org/10.1002/ange.200901928.

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45

Xi, Zhenfeng, and Pixu Li. "Aluminiumtrichlorid- und Zirconocen-vermittelte Desoxygenierung und Cycloaddition von Aldehyden an Alkine unter Bildung von Cyclopentadienderivaten." Angewandte Chemie 112, no. 16 (August 18, 2000): 3057–59. http://dx.doi.org/10.1002/1521-3757(20000818)112:16<3057::aid-ange3057>3.0.co;2-y.

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46

Liu, Xiaocui, Wenbo Ming, Alexandra Friedrich, Florian Kerner, and Todd B. Marder. "Kupfer‐katalysierte Triborierung terminaler Alkine mit B 2 pin 2 : Effiziente Synthese von 1,1,2‐Triborylalkenen." Angewandte Chemie 132, no. 1 (November 19, 2019): 311–16. http://dx.doi.org/10.1002/ange.201908466.

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47

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Sünkel, Karlheinz, and Doris Motz. "Komplexchemie perhalogenierter Cyclopentadiene und Alkine, I. Metallierung von (C5Cl4Br)Mn(CO)3 und Umsetzungen mit Elektrophilen." Chemische Berichte 121, no. 4 (April 1988): 799–801. http://dx.doi.org/10.1002/cber.19881210428.

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Bader, Hubert, Henning Hopf, and Helge Jäger. "Alkine und Cumulene, XXI. 2-Ethinyl-1,3-butadien – ein neues Dien für die Diels-Alder-Reaktion." Chemische Berichte 122, no. 6 (June 1989): 1193–98. http://dx.doi.org/10.1002/cber.19891220627.

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Hopf, Henning, Reiner Stamm, and Peter G. Jones. "Alkine und Cumulene, XXIII. über einige Neben- und Folgeprodukte der Dichlorketen-Herstellung aus α,α-Dichloracetylchlorid." Chemische Berichte 124, no. 5 (May 1991): 1291–94. http://dx.doi.org/10.1002/cber.19911240548.

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