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Journal articles on the topic 'Addition de Michael diastéréosélective'

Author: Grafiati

Published: 4 June 2021

Last updated: 3 February 2022

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1

Pourcelot, G., J. Aubouet, A. Caspar, and P. Cresson. "Addition diastéréosélective d'organo-cuprates à des imides chirales insaturées." Journal of Organometallic Chemistry 328, no. 3 (July 1987): C43—C45. http://dx.doi.org/10.1016/0022-328x(87)80264-4.

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2

Pourcelot, G., O. Melnyk, Y. Besace, E. Stephan, and P. Cresson. "Addition diastéréosélective d'allyl cuprates à des imides chirales insaturées." Journal of Organometallic Chemistry 388, no. 1-2 (May 1990): c5—c8. http://dx.doi.org/10.1016/0022-328x(90)85369-a.

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3

Thanupran, Chatchai, Chachanat Thebtaranonth, and Yodhathai Thebtaranonth. "Stereospecific triple Michael addition." Tetrahedron Letters 27, no. 20 (1986): 2295–98. http://dx.doi.org/10.1016/s0040-4039(00)84512-8.

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4

Liao, Xi-Bin, Ji-Ye Han, and Ying Li. "Michael addition of artemisitene." Tetrahedron Letters 42, no. 15 (April 2001): 2843–45. http://dx.doi.org/10.1016/s0040-4039(01)00310-0.

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5

Reuter, Carin, and Fritz Vögtle. "Rotaxanes via Michael Addition†." Organic Letters 2, no. 5 (March 2000): 593–95. http://dx.doi.org/10.1021/ol990350u.

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6

Feil, Sylvia. "Wundverschluss durch Michael-Addition?" Chemie in unserer Zeit 39, no. 4 (August 2005): 233. http://dx.doi.org/10.1002/ciuz.200590050.

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7

Thirumalaikumar, Muniappan. "Enantioselective Michael Addition Reactions." Organic Preparations and Procedures International 43, no. 1 (February 10, 2011): 67–129. http://dx.doi.org/10.1080/00304948.2011.547102.

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8

Jha, S. C., and N. N. Joshi. "Catalytic, enatioselective Michael addition reactions." Arkivoc 2002, no. 7 (September 20, 2002): 167–96. http://dx.doi.org/10.3998/ark.5550190.0003.718.

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9

Trumbo, David L. "Michael addition polymers from bisacetoacetates." Polymer Bulletin 26, no. 5 (September 1991): 481–85. http://dx.doi.org/10.1007/bf01032670.

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10

Chen, Bi-Shuang, Verena Resch, Linda G. Otten, and Ulf Hanefeld. "Enantioselective Michael Addition of Water." Chemistry - A European Journal 21, no. 7 (December 21, 2014): 3020–30. http://dx.doi.org/10.1002/chem.201405579.

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11

Alexakis, A., and K. Li. "Enantioselective Michael Addition-Cyclization Reaction." Synfacts 2007, no. 7 (July 2007): 0738. http://dx.doi.org/10.1055/s-2007-968672.

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12

Hutchinson, David W., and David M. Thornton. "Michael addition reactions of ethenylidenebisphosphonates." Journal of Organometallic Chemistry 346, no. 3 (June 1988): 341–48. http://dx.doi.org/10.1016/0022-328x(88)80134-7.

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13

Wang, Tai-chi, Yeh-Long Chen, Kuan-Han Lee, and Cherng-Chyi Tzeng. "An intermolecular Michael addition of benzene." Tetrahedron Letters 37, no. 35 (August 1996): 6369–70. http://dx.doi.org/10.1016/0040-4039(96)01364-0.

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14

Vieth, Siegfried, Burkhard Costisella, and Matthias Schneider. "Tandem Michael addition alkylation of vinylphosphonates." Tetrahedron 53, no. 28 (July 1997): 9623–28. http://dx.doi.org/10.1016/s0040-4020(97)00648-0.

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15

Li, Hao, Liansuo Zu, Hexin Xie, Jian Wang, Wei Jiang, and Wei Wang. "Enantioselective Organocatalytic Double Michael Addition Reactions." Organic Letters 9, no. 9 (April 2007): 1833–35. http://dx.doi.org/10.1021/ol070581y.

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16

Błażewska, Katarzyna, Joanna Gmach, and Łukasz Joachimiak. "Aza-Michael Addition of Imidazole Analogues." Synthesis 48, no. 17 (August 15, 2016): 2681–704. http://dx.doi.org/10.1055/s-0035-1560451.

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17

Tang, Y., Q. G. Wang, X. M. Deng, B. H. Zhu, L. W. Ye, X. L. Sun, C. Y. Li, C. Y. Zhu, and Q. Shen. "Domino Asymmetric Michael Addition/Ylide Epoxidation." Synfacts 2008, no. 7 (July 2008): 0711. http://dx.doi.org/10.1055/s-2008-1078455.

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18

Tsuboi, Sadao, Hiroyuki Nagae, Hirofumi Yamato, and Akira Takeda. "A Michael Addition-Induced Favorskii Rearrangement." Bulletin of the Chemical Society of Japan 60, no. 2 (February 1987): 836–38. http://dx.doi.org/10.1246/bcsj.60.836.

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19

Müh, Ekkehard, Hans Weickmann, Joachim E. Klee, Holger Frey, and Rolf Mülhaupt. "Acrylate-Terminated Macromonomers by Michael Addition." Macromolecular Chemistry and Physics 202, no. 18 (December 1, 2001): 3484–89. http://dx.doi.org/10.1002/1521-3935(20011201)202:18<3484::aid-macp3484>3.0.co;2-l.

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20

Hamlin, Trevor A., Israel Fernández, and F. Matthias Bickelhaupt. "How Dihalogens Catalyze Michael Addition Reactions." Angewandte Chemie International Edition 58, no. 26 (June 24, 2019): 8922–26. http://dx.doi.org/10.1002/anie.201903196.

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21

Deng, L., and X. Lu. "Broad Scope Organocatalytic Aza-Michael Addition." Synfacts 2008, no. 11 (October 23, 2008): 1222. http://dx.doi.org/10.1055/s-0028-1083385.

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22

Mukaiyama, T., T. Tozawa, H. Nagao, and Y. Yamane. "Asymmetric Domino Mukaiyama-Michael-Addition-Lactonization." Synfacts 2007, no. 3 (March 2007): 0318. http://dx.doi.org/10.1055/s-2007-968233.

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23

Reddy, S. Madhava, and H. M. Walborsky. "A facile intramolecular Michael addition reaction." Journal of Organic Chemistry 51, no. 13 (June 1986): 2605–7. http://dx.doi.org/10.1021/jo00363a042.

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24

Wang, X., R. T. Li, X. Ai, J. M. Liu, Z. M. Ge, and T. M. Cheng. "Aza-Michael Addition in Alkaline Al2O3." Synfacts 2010, no. 09 (August 23, 2010): 1089. http://dx.doi.org/10.1055/s-0030-1257984.

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25

You, S. L., Q. Cai, and C. Zheng. "Intramolecular Aza-Michael Addition of Indoles." Synfacts 2010, no. 12 (November 22, 2010): 1428. http://dx.doi.org/10.1055/s-0030-1258922.

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26

Pansare, S., and K. Pandya. "Amine/Protonic Acid Catalyzed Michael Addition." Synfacts 2006, no. 9 (September 2006): 0955. http://dx.doi.org/10.1055/s-2006-949231.

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27

Thirumalaikumar, Muniappan. "ChemInform Abstract: Enantioselective Michael Addition Reactions." ChemInform 42, no. 31 (July 7, 2011): no. http://dx.doi.org/10.1002/chin.201131260.

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28

Yu, Mirim, and Sung-Gon Kim. "Asymmetric organocatalytic Michael addition/aza-cyclization coupled with sequential Michael addition for synthesizing densely polycyclic-fused dihydroquinolines." Tetrahedron Letters 56, no. 28 (July 2015): 4159–62. http://dx.doi.org/10.1016/j.tetlet.2015.04.112.

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29

Wu, Zhi-Jun, Shi-Wei Luo, Jian-Wu Xie, Xiao-Ying Xu, Dong-Mei Fang, and Guo-Lin Zhang. "Study of michael-michael-retro michael addition catalyzed by 9-amino-9-deoxyepiquinine using ESI-MS." Journal of the American Society for Mass Spectrometry 18, no. 11 (November 2007): 2074–80. http://dx.doi.org/10.1016/j.jasms.2007.09.002.

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30

Bremand, Nathalie, Ilan Marek, and Jean F. Normant. "Regioselective addition ofnbutyllithium on secondary cinnamyl amides: “Michael" versus “contra-Michael" process." Tetrahedron Letters 40, no. 17 (April 1999): 3379–82. http://dx.doi.org/10.1016/s0040-4039(99)00494-3.

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31

Lalthanpuii, P. B., C. Lalhriatpuia, and K. Vanlaldinpuia. "Asymmetric Michael addition using sugar derived organocatalysts." Science Vision 17, no. 4 (December 31, 2017): 182–96. http://dx.doi.org/10.33493/scivis.17.04.02.

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Abstract:

Sugars are low-molecular-weight carbohydrates which consist of polyhydroxyl and carbonyl (aldehyde or ketone) functional groups. Different types of compounds derived from sugars have been used extensively as powerful and effective catalysts for asymmetric synthesis. They are readily available at a reasonable price, easily prepared, no metal contamination and are inert towards moisture and air. They are highly functionalized and have well defined stereogenic centres. Most of them are employed as chiral ligands in metal based asymmetric catalysis and are used for various asymmetric transformations. Different compounds derived from sugars have also been used recently as organocatalysts for asymmetric synthesis. The present article provides some of the organocatalysts used for asymmetric synthesis.

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32

Bakó, Péter, Tamás Nemcsok, Zsolt Rapi, and György Keglevich. "Enantioselective Michael Addition of Malonates to Enones." Current Organic Chemistry 24, no. 7 (June 3, 2020): 746–73. http://dx.doi.org/10.2174/1385272824666200316122221.

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Abstract:

: Many catalysts were tested in asymmetric Michael additions in order to synthesize enantioenriched products. One of the most common reaction types among the Michael reactions is the conjugated addition of malonates to enones making it possible to investigate the structure–activity relationship of the catalysts. The most commonly used Michael acceptors are chalcone, substituted chalcones, chalcone derivatives, cyclic enones, while typical donors may be dimethyl, diethyl, dipropyl, diisopropyl, dibutyl, di-tert-butyl and dibenzyl malonates. This review summarizes the most important enantioselective catalysts applied in these types of reactions.

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33

Gibas, Mirosław, and Anna Korytkowska-Wałach. "Oligomerisation of hydroxymethacrylates via Michael-type addition." Polymer 44, no. 14 (June 2003): 3811–16. http://dx.doi.org/10.1016/s0032-3861(03)00333-1.

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34

Zahouily, Mohamed, Younes Abrouki, and Ahmed Rayadh. "Na2CaP2O7, a new catalyst for Michael addition." Tetrahedron Letters 43, no. 43 (October 2002): 7729–30. http://dx.doi.org/10.1016/s0040-4039(02)01846-4.

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35

Zahouily, Mohamed, Younes Abrouki, Ahmed Rayadh, Saı̈d Sebti, Hamid Dhimane, and Marc David. "Fluorapatite: efficient catalyst for the Michael addition." Tetrahedron Letters 44, no. 12 (March 2003): 2463–65. http://dx.doi.org/10.1016/s0040-4039(03)00323-x.

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36

Ye, Rong, Franco F. Faucher, and Gabor A. Somorjai. "Supported iron catalysts for Michael addition reactions." Molecular Catalysis 447 (March 2018): 65–71. http://dx.doi.org/10.1016/j.mcat.2017.12.029.

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37

Clausen, Thomas P., Beverly Johnson, and Jim Wood. "A Mixed Aldol Condensation-Michael Addition Experiment." Journal of Chemical Education 73, no. 3 (March 1996): 266. http://dx.doi.org/10.1021/ed073p266.

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38

Kang, Qiang, and Yugen Zhang. "N-Heterocyclic carbene-catalyzed aza-Michael addition." Organic & Biomolecular Chemistry 9, no. 19 (2011): 6715. http://dx.doi.org/10.1039/c1ob05429e.

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39

Yang, Hongjun, YongKang Zuo, Jiadong Zhang, Yiye Song, Wenyan Huang, Xiaoqiang Xue, Qimin Jiang, Aibin Sun, and Bibiao Jiang. "Phosphazene-catalyzed oxa-Michael addition click polymerization." Polymer Chemistry 9, no. 38 (2018): 4716–23. http://dx.doi.org/10.1039/c8py01089g.

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40

Du, D. M., S. F. Lu, J. Xu, and S. W. Zhang. "Catalyzed Michael Addition of Nitroalkanes to Nitroalkenes." Synfacts 2006, no. 9 (September 2006): 0908. http://dx.doi.org/10.1055/s-2006-949234.

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41

Ricci, Alfredo, Gabriele Micheletti, Salvatore Pollicino, Guillaume Berionni, and Gérard Cahiez. "Michael Addition of Manganese Enolates to Nitroolefins." Synlett 2007, no. 18 (October 12, 2007): 2829–32. http://dx.doi.org/10.1055/s-2007-991096.

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42

Wang, Liang, Jian Xiao, Huaili Zhao, and Xiaoxiao Wang. "Regioselective Michael Addition of Anthrone to Methyleneindolinones." Synthesis 48, no. 13 (April 18, 2016): 2112–20. http://dx.doi.org/10.1055/s-0035-1561593.

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43

Kumar, Atul, and Akanksha. "Amino acid catalyzed thio-Michael addition reactions." Tetrahedron 63, no. 45 (November 2007): 11086–92. http://dx.doi.org/10.1016/j.tet.2007.08.033.

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44

Gliese, Jan-Philipp, Stefan H. Jungbauer, and Stefan M. Huber. "A halogen-bonding-catalyzed Michael addition reaction." Chemical Communications 53, no. 88 (2017): 12052–55. http://dx.doi.org/10.1039/c7cc07175b.

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45

Li, Wenjun, Wenbin Wu, Feng Yu, Huicai Huang, Xinmiao Liang, and Jinxing Ye. "Catalytic asymmetric Michael addition with curcumin derivative." Organic & Biomolecular Chemistry 9, no. 7 (2011): 2505. http://dx.doi.org/10.1039/c0ob00757a.

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46

Zhang, Xiaojie, Jinling Li, Hemi Qu, Chunyan Chi, and Jishan Wu. "Fused Bispentacenequinone and Its Unexpected Michael Addition." Organic Letters 12, no. 17 (September 3, 2010): 3946–49. http://dx.doi.org/10.1021/ol101720e.

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47

Wang, W., J. Wang, H. Li, and L. Zu. "Enantioselective Michael Addition ofN-Heterocycles to Nitroolefins." Synfacts 2006, no. 6 (June 2006): 0609. http://dx.doi.org/10.1055/s-2006-941779.

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48

Kanger, T., S. Mossé, M. Laars, K. Kriis, and A. Alexakis. "Michael Addition Catalyzed by a Chiral Bimorpholine." Synfacts 2006, no. 7 (June 2006): 0728. http://dx.doi.org/10.1055/s-2006-941906.

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49

Ramb, Daniel C., Andreas Lerchen, Marvin Kischkewitz, Bernd Beutel, Santos Fustero, and Günter Haufe. "Addition of Nucleophiles to Fluorinated Michael Acceptors." European Journal of Organic Chemistry 2016, no. 9 (March 2016): 1751–59. http://dx.doi.org/10.1002/ejoc.201600088.

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50

Enders, Dieter, Alexandre Saint-Dizier, Marie-Isabelle Lannou, and Achim Lenzen. "The Phospha-Michael Addition in Organic Synthesis." European Journal of Organic Chemistry 2006, no. 1 (January 2006): 29–49. http://dx.doi.org/10.1002/ejoc.200500593.

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