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Journal articles on the topic 'Enantiodivergent'

Author: Grafiati

Published: 4 June 2021

Last updated: 15 February 2022

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1

Westermann, Bernhard, Muhammad Ayaz, and Sander S van Berkel. "Enantiodivergent Organocascade Reactions." Angewandte Chemie International Edition 49, no. 5 (December 22, 2009): 846–49. http://dx.doi.org/10.1002/anie.200904638.

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2

Sohtome, Yoshihiro, and Kazuo Nagasawa. "Sequential stereodivergent organocatalysis and programmed organocascades." Org. Biomol. Chem. 12, no. 11 (2014): 1681–85. http://dx.doi.org/10.1039/c3ob42310g.

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3

Geiger, Yannick, Thierry Achard, Aline Maisse-François, and Stéphane Bellemin-Laponnaz. "Hyperpositive non-linear effects: enantiodivergence and modelling." Chemical Science 11, no. 46 (2020): 12453–63. http://dx.doi.org/10.1039/d0sc04724d.

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4

Cao, Weidi, Xiaoming Feng, and Xiaohua Liu. "Reversal of enantioselectivity in chiral metal complex-catalyzed asymmetric reactions." Organic & Biomolecular Chemistry 17, no. 27 (2019): 6538–50. http://dx.doi.org/10.1039/c9ob01027k.

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5

Sivamuthuraman, Koilpitchai, and Venkitasamy Kesavan. "Catalytic enantioselective Michael addition of 2-substituted benzofuran-3-ones to 2-enoyl pyridines." Organic & Biomolecular Chemistry 17, no. 30 (2019): 7166–71. http://dx.doi.org/10.1039/c9ob01069f.

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6

Oczipka, P., D. Müller, W. Leitner, and G. Franciò. "Enantiodivergent asymmetric catalysis with the tropos BIPHEP ligand and a proline derivative as chiral selector." Chemical Science 7, no. 1 (2016): 678–83. http://dx.doi.org/10.1039/c5sc03465e.

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7

Chen, Chien-Tien, Cheng-Che Tsai, Pei-Kang Tsou, Gou-Tao Huang, and Chin-Hui Yu. "Enantiodivergent Steglich rearrangement of O-carboxylazlactones catalyzed by a chirality switchable helicene containing a 4-aminopyridine unit." Chemical Science 8, no. 1 (2017): 524–29. http://dx.doi.org/10.1039/c6sc02646j.

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8

Nagamoto, Midori, Daisuke Yamauchi, and Takahiro Nishimura. "Iridium-catalyzed asymmetric [3+2] annulation of aromatic ketimines with alkynes via C–H activation: unexpected inversion of the enantioselectivity induced by protic acids." Chemical Communications 52, no. 34 (2016): 5876–79. http://dx.doi.org/10.1039/c6cc01398h.

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9

Xie, Shaolei, Zhi-Juan He, Ling-Hui Zhang, Bo-Lun Huang, Xiao-Wei Chen, Zong-Song Zhan, and Fu-Min Zhang. "The organocatalytic enantiodivergent fluorination of β-ketodiaryl-phosphine oxides for the construction of carbon-fluorine quaternary stereocenters." Chemical Communications 57, no. 16 (2021): 2069–72. http://dx.doi.org/10.1039/d0cc07770d.

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We developed, for the first time, the cinchona-alkaloid-catalyzed enantiodivergent α-fluorination of β-keto diarylphosphine oxides, which resulted in two enantiomers bearing fluorine-containing quaternary stereocenters.

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10

Pazos, Gonzalo, Manuel Pérez, Zoila Gándara, Generosa Gómez, and Yagamare Fall. "Enantiodivergent synthesis of (+)- and (−)-isolaurepan." Tetrahedron 68, no. 44 (November 2012): 8994–9003. http://dx.doi.org/10.1016/j.tet.2012.08.094.

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11

Ferrer, Èric, Ramon Alibés, Félix Busqué, Marta Figueredo, Josep Font, and Pedro de March. "Enantiodivergent Synthesis of Cyclohexenyl Nucleosides." Journal of Organic Chemistry 74, no. 6 (March 20, 2009): 2425–32. http://dx.doi.org/10.1021/jo802492g.

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12

Chan, Yuk-Cheung, Xinyan Wang, Ying-Pong Lam, Jonathan Wong, Ying-Lung Steve Tse, and Ying-Yeung Yeung. "A Catalyst-Controlled Enantiodivergent Bromolactonization." Journal of the American Chemical Society 143, no. 32 (August 5, 2021): 12745–54. http://dx.doi.org/10.1021/jacs.1c05680.

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13

Massaro, Luca, Jia Zheng, Cristiana Margarita, and Pher G. Andersson. "Enantioconvergent and enantiodivergent catalytic hydrogenation of isomeric olefins." Chemical Society Reviews 49, no. 8 (2020): 2504–22. http://dx.doi.org/10.1039/c9cs00138g.

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In the asymmetric hydrogenation of olefins the enantiodivergent outcome is predominant. However, the less common enantioconvergent phenomenon affords significant practical advantages, such as the possibility to hydrogenate mixtures of E/Z alkenes.

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14

Takano, Seiichi, Minoru Moriya, and Kunio Ogasawara. "Concise enantiodivergent synthesis of eutypoxide B." Journal of the Chemical Society, Chemical Communications, no. 7 (1993): 614. http://dx.doi.org/10.1039/c39930000614.

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15

Chaux, Fanny, Slawomir Frynas, Hugo Laureano, Christine Salomon, Gérald Morata, Marie-Laure Auclair, Michel (Massoud) Stephan, et al. "Enantiodivergent synthesis of P-chirogenic phosphines." Comptes Rendus Chimie 13, no. 8-9 (August 2010): 1213–26. http://dx.doi.org/10.1016/j.crci.2010.06.001.

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16

Demnitz, Joachim, Luigi LaVecchia, Edmond Bacher, Thomas Keller, Thomas Müller, Friedrich Schürch, Hans-Peter Weber, and Esteban Pombo-Villar. "Enantiodivergent Synthesis of (R)- and (S)-Rolipram." Molecules 3, no. 8 (March 10, 1998): 107–19. http://dx.doi.org/10.3390/30300107.

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17

Mehta, Goverdhan, Ramesh Samineni, and Pabbaraja Srihari. "An enantiodivergent formal synthesis of paecilomycine A." Tetrahedron Letters 53, no. 7 (February 2012): 829–32. http://dx.doi.org/10.1016/j.tetlet.2011.12.015.

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18

Labora, Maitia, Enrique M. Pandolfi, and Valeria Schapiro. "Efficient enantiodivergent total synthesis of (+) and (−)-bromoxone." Tetrahedron: Asymmetry 21, no. 2 (February 2010): 153–55. http://dx.doi.org/10.1016/j.tetasy.2009.12.016.

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19

Hudlicky, Tomas, John D. Price, Fan Rulin, and Toshiya Tsunoda. "Efficient and enantiodivergent synthesis of (+)- and (-)-pinitol." Journal of the American Chemical Society 112, no. 25 (December 1990): 9439–40. http://dx.doi.org/10.1021/ja00181a081.

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20

Leisch, Hannes, Alvaro T. Omori, Kevin J. Finn, Jacqueline Gilmet, Tyler Bissett, David Ilceski, and Tomáš Hudlický. "Chemoenzymatic enantiodivergent total syntheses of (+)- and (−)-codeine." Tetrahedron 65, no. 47 (November 2009): 9862–75. http://dx.doi.org/10.1016/j.tet.2009.09.052.

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21

Rajesh, B. M., Madhuri V. Shinde, M. Kannan, Gujjary Srinivas, Javed Iqbal, and D. Srinivasa Reddy. "Enantiodivergent routes to (+) and (−)-novioses from (−)-pantolactone." RSC Advances 3, no. 43 (2013): 20291. http://dx.doi.org/10.1039/c3ra42891e.

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22

Riehl, Paul S., Alistair D. Richardson, Tatsuhiro Sakamoto, and Corinna S. Schindler. "Eight-Step Enantiodivergent Synthesis of (+)- and (−)-Lingzhiol." Organic Letters 22, no. 1 (December 19, 2019): 290–94. http://dx.doi.org/10.1021/acs.orglett.9b04322.

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23

Takano, Seiichi, Yasuhiro Higashi, Takashi Kamikubo, Minoru Moriya, and Kunio Ogasawara. "Enantiodivergent Preparation of Chiral 2,5-Cyclohexadienone Synthons." Synthesis 1993, no. 10 (1993): 948–50. http://dx.doi.org/10.1055/s-1993-25973.

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24

Bartali, Laura, Andrea Casini, Antonio Guarna, Ernesto G. Occhiato, and Dina Scarpi. "Enantiodivergent Chemoenzymatic Synthesis of 4-Hydroxypiperidine Alkaloids." European Journal of Organic Chemistry 2010, no. 30 (August 31, 2010): 5831–40. http://dx.doi.org/10.1002/ejoc.201000837.

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25

Macharia, Juliet, Victor Wambua, Yun Hong, Lawrence Harris, Jennifer S. Hirschi, Gary B. Evans, and Mathew J. Vetticatt. "A Designed Approach to Enantiodivergent Enamine Catalysis." Angewandte Chemie International Edition 56, no. 30 (June 20, 2017): 8756–60. http://dx.doi.org/10.1002/anie.201703919.

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26

Wang, Jianmin, Jie Chen, Choon Wee Kee, and Choon-Hong Tan. "Enantiodivergent and γ-Selective Asymmetric Allylic Amination." Angewandte Chemie 124, no. 10 (January 27, 2012): 2432–36. http://dx.doi.org/10.1002/ange.201107317.

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27

Sasaki, Michiko, Tomo Takegawa, Kunihiro Sakamoto, Yuri Kotomori, Yuko Otani, Tomohiko Ohwada, Masatoshi Kawahata, Kentaro Yamaguchi, and Kei Takeda. "Enantiodivergent Deprotonation/Acylation of α-Amino Nitriles." Angewandte Chemie International Edition 52, no. 49 (October 9, 2013): 12956–60. http://dx.doi.org/10.1002/anie.201306443.

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28

Macharia, Juliet, Victor Wambua, Yun Hong, Lawrence Harris, Jennifer S. Hirschi, Gary B. Evans, and Mathew J. Vetticatt. "A Designed Approach to Enantiodivergent Enamine Catalysis." Angewandte Chemie 129, no. 30 (June 20, 2017): 8882–86. http://dx.doi.org/10.1002/ange.201703919.

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29

Sasaki, Michiko, Tomo Takegawa, Kunihiro Sakamoto, Yuri Kotomori, Yuko Otani, Tomohiko Ohwada, Masatoshi Kawahata, Kentaro Yamaguchi, and Kei Takeda. "Enantiodivergent Deprotonation/Acylation of α-Amino Nitriles." Angewandte Chemie 125, no. 49 (October 9, 2013): 13194–98. http://dx.doi.org/10.1002/ange.201306443.

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30

Wang, Jianmin, Jie Chen, Choon Wee Kee, and Choon-Hong Tan. "Enantiodivergent and γ-Selective Asymmetric Allylic Amination." Angewandte Chemie International Edition 51, no. 10 (January 27, 2012): 2382–86. http://dx.doi.org/10.1002/anie.201107317.

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31

Leiva de Faria, Mary, Ruy de A. Magalhães, Fernando C. Silva, Luiz G. de O. Matias, Marco A. Ceschi, Ursula Brocksom, and Timothy John Brocksom. "Enantiodivergent syntheses of cycloheptenone intermediates for guaiane sesquiterpenes." Tetrahedron: Asymmetry 11, no. 20 (October 2000): 4093–103. http://dx.doi.org/10.1016/s0957-4166(00)00387-6.

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32

Suzuki, Katsufumi, Muneo Shoji, Eriko Kobayashi, and Kohei Inomata. "Concise enantiodivergent synthesis of (+)- and (−)-trans-quercus lactones." Tetrahedron: Asymmetry 12, no. 20 (November 2001): 2789–92. http://dx.doi.org/10.1016/s0957-4166(01)00500-6.

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33

Aggarwal, V., J. Stymiest, V. Bagutski, and R. French. "Enantiodivergent Synthesis of Tertiary Alcohols from Secondary Carbamates." Synfacts 2009, no. 03 (February 19, 2009): 0284. http://dx.doi.org/10.1055/s-0028-1087778.

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34

Fox, Martin E., Chi Li, Joseph P. Marino, and Larry E. Overman. "Enantiodivergent Total Syntheses of (+)- and (−)-Scopadulcic Acid A." Journal of the American Chemical Society 121, no. 23 (June 1999): 5467–80. http://dx.doi.org/10.1021/ja990404v.

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35

Tu, Hang-Fei, Pusu Yang, Zi-Hua Lin, Chao Zheng, and Shu-Li You. "Time-dependent enantiodivergent synthesis via sequential kinetic resolution." Nature Chemistry 12, no. 9 (June 29, 2020): 838–44. http://dx.doi.org/10.1038/s41557-020-0489-1.

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36

Hedouin, Gaspard, and Françoise Colobert. "An Extraordinary Catalyst Allowing Time-Dependent Enantiodivergent Synthesis." Chem 6, no. 8 (August 2020): 1858–60. http://dx.doi.org/10.1016/j.chempr.2020.07.016.

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37

Biswas, Tanmoy, Jyoti Prasad Mukherjee, and Shital K. Chattopadhyay. "Enantiodivergent synthesis of N-protected azetidine-2-carboxylic acid." Tetrahedron: Asymmetry 23, no. 18-19 (October 2012): 1416–22. http://dx.doi.org/10.1016/j.tetasy.2012.08.016.

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38

Sano, Shigeki, Michiyasu Nakao, Masanori Takeyasu, Chiyo Yamamoto, Syuji Kitaike, Yasuko Yoshioka, and Yoshimitsu Nagao. "Chemoenzymatic Synthesis of α-Substituted Serines via Enantiodivergent Transformation." Open Organic Chemistry Journal 3, no. 1 (February 10, 2009): 22–34. http://dx.doi.org/10.2174/1874095200903010022.

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39

Prasad, Kavirayani R., and Kamala Penchalaiah. "Enantiodivergent total synthesis of microcarpalide from l-tartaric acid." Tetrahedron 67, no. 23 (June 2011): 4268–76. http://dx.doi.org/10.1016/j.tet.2011.03.102.

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40

Wang, Xu, Jie Li, Ralph A. Saporito, and Naoki Toyooka. "Enantiodivergent synthesis of the quinolizidine poison frog alkaloid 195C." Tetrahedron 69, no. 48 (December 2013): 10311–15. http://dx.doi.org/10.1016/j.tet.2013.10.009.

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41

Ghosh, Manju, Sritama Bose, Soumitra Maity, and Subrata Ghosh. "Enantiodivergent synthesis of (−)-methylenolactocin and (+)-methylenolactocin from d-mannitol." Tetrahedron Letters 50, no. 50 (December 2009): 7102–4. http://dx.doi.org/10.1016/j.tetlet.2009.10.011.

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42

Barco, Achille, Nikla Baricordi, Simonetta Benetti, Carmela De Risi, Gian P. Pollini, and Vinicio Zanirato. "A new enantiodivergent synthesis of the Geissman–Waiss lactone." Tetrahedron 63, no. 20 (May 2007): 4278–83. http://dx.doi.org/10.1016/j.tet.2007.03.056.

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43

Stymiest, Jake L., Viktor Bagutski, Rosalind M. French, and Varinder K. Aggarwal. "Enantiodivergent conversion of chiral secondary alcohols into tertiary alcohols." Nature 456, no. 7223 (December 2008): 778–82. http://dx.doi.org/10.1038/nature07592.

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44

Saha, Nemai, Tanmoy Biswas, and Shital K. Chattopadhyay. "Enantiodivergent Synthetic Entry to the Quinolizidine Alkaloid Lasubine II." Organic Letters 13, no. 19 (October 7, 2011): 5128–31. http://dx.doi.org/10.1021/ol2019967.

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45

Sardina, F. Javier, Michael H. Howard, Marshall Morningstar, and Henry Rapoport. "Enantiodivergent synthesis of (+)- and (-)-anatoxin from L-glutamic acid." Journal of Organic Chemistry 55, no. 17 (August 1990): 5025–33. http://dx.doi.org/10.1021/jo00304a012.

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46

Sohtome, Yoshihiro, and Kazuo Nagasawa. "Dynamic Enantiodivergent Organocatalysis: Merging Molecular Motors with Bifunctional Organocatalysts." ChemPhysChem 12, no. 12 (May 31, 2011): 2217–19. http://dx.doi.org/10.1002/cphc.201100335.

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47

TAKANO, S., Y. HIGASHI, T. KAMIKUBO, M. MORIYA, and K. OGASAWARA. "ChemInform Abstract: Enantiodivergent Preparation of Chiral 2,5-Cyclohexadienone Synthons." ChemInform 25, no. 11 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199411060.

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48

TAKANO, S., M. MORIYA, and K. OGASAWARA. "ChemInform Abstract: Concise Enantiodivergent Synthesis of Eutypoxide B (I)." ChemInform 24, no. 29 (August 20, 2010): no. http://dx.doi.org/10.1002/chin.199329271.

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49

Wang, Jianmin, Jie Chen, Choon Wee Kee, and Choon-Hong Tan. "ChemInform Abstract: Enantiodivergent and γ-Selective Asymmetric Allylic Amination." ChemInform 43, no. 28 (June 14, 2012): no. http://dx.doi.org/10.1002/chin.201228037.

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50

Sasaki, Michiko, Tomo Takegawa, Kunihiro Sakamoto, Yuri Kotomori, Yuko Otani, Tomohiko Ohwada, Masatoshi Kawahata, Kentaro Yamaguchi, and Kei Takeda. "ChemInform Abstract: Enantiodivergent Deprotonation/Acylation of α-Amino Nitriles." ChemInform 45, no. 19 (April 23, 2014): no. http://dx.doi.org/10.1002/chin.201419073.

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