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Journal articles on the topic 'C2-symmetric'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Meyers, A. "C2 Symmetric Amines. I. The Asymmetric Ullmann Synthesis of a New C2-Symmetric Binaphthyl." Tetrahedron Letters 36, no. 33 (1995): 5869–72. http://dx.doi.org/10.1016/00404-0399(50)1180p-.

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2

Quallich, G. "Enantioselective Synthesis of C2-Symmetric Diols." Tetrahedron Letters 36, no. 27 (1995): 4729–32. http://dx.doi.org/10.1016/00404-0399(50)0889k-.

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3

MEYERS, A. I., and M. J. MCKENNON. "ChemInform Abstract: C2-Symmetric Amines. Part 1. The Asymmetric Ullmann Synthesis of a New C2-Symmetric Binaphthyl." ChemInform 26, no. 48 (2010): no. http://dx.doi.org/10.1002/chin.199548045.

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4

Tanner, David, and Carin Birgersson. "C2-symmetric aziridines as efficient chiral auxiliaries." Tetrahedron Letters 32, no. 22 (1991): 2533–36. http://dx.doi.org/10.1016/s0040-4039(00)74374-7.

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5

Mitra, Tapobrata, Sanket Das, and Amit Basak. "Synthesis of C2-symmetric bis-indolyl sulfones." Tetrahedron Letters 50, no. 42 (2009): 5846–49. http://dx.doi.org/10.1016/j.tetlet.2009.08.001.

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6

Chen, Zhuoliang, and Ronald L. Halterman. "Asymmetric Synthesis of C2-Symmetric Annulated Bicyclooctylcyclopentadienes." Synlett 1990, no. 02 (1990): 103–5. http://dx.doi.org/10.1055/s-1990-21001.

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7

Kanger, Tõnis, Kadri Kriis, Tõnis Pehk, Aleksander-Mati Müürisepp, and Margus Lopp. "Asymmetric synthesis of novel C2-symmetric bimorpholines." Tetrahedron: Asymmetry 13, no. 8 (2002): 857–65. http://dx.doi.org/10.1016/s0957-4166(02)00188-x.

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8

Chen, Feng, Chong Kiat Tan, and Ying-Yeung Yeung. "C2-Symmetric Cyclic Selenium-Catalyzed Enantioselective Bromoaminocyclization." Journal of the American Chemical Society 135, no. 4 (2013): 1232–35. http://dx.doi.org/10.1021/ja311202e.

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9

Voronova, L. N., I. A. Tolmacheva, V. V. Grishko, and A. G. Tolstikov. "Synthesis of C2 symmetric triterpene bis-enaminones." Chemistry of Natural Compounds 48, no. 1 (2012): 75–82. http://dx.doi.org/10.1007/s10600-012-0162-z.

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10

Gurjar, Mukund K., Shashwati Pal, A. V. Rama Rao, Richard J. Pariza, and Mukund S. Chorghade. "Synthesis of novel C2-symmetric and pseudo C2-symmetric based diols, epoxides and dideoxy derivatives of HIV protease inhibitors." Tetrahedron 53, no. 13 (1997): 4769–78. http://dx.doi.org/10.1016/s0040-4020(97)00160-9.

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11

Huynh, Khoi, Bryon K. Anderson, and Tom Livinghouse. "Enantioselective hydroamination/cyclization of aminoalkenes by (bis)-C2 symmetric and (mono)-C2 symmetric anionic tetraamide complexes of La(III)." Tetrahedron Letters 56, no. 23 (2015): 3658–61. http://dx.doi.org/10.1016/j.tetlet.2015.03.044.

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12

Kempf, Dale J., Thomas J. Sowin, Elizabeth M. Doherty, et al. "Stereocontrolled synthesis of C2-symmetric and pseudo-C2-symmetric diamino alcohols and diols for use in HIV protease inhibitors." Journal of Organic Chemistry 57, no. 21 (1992): 5692–700. http://dx.doi.org/10.1021/jo00047a023.

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13

Boulch, Rachel, Andreas Scheurer, Paul Mosset, and Rolf W. Saalfrank. "Asymmetric cyclopropanation catalyzed by C2-symmetric bi(oxazolines)." Tetrahedron Letters 41, no. 7 (2000): 1023–26. http://dx.doi.org/10.1016/s0040-4039(99)02220-0.

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14

Thaharn, Watcharaporn, Darunee Soorukram, Chutima Kuhakarn, Vichai Reutrakul, and Manat Pohmakotr. "Synthesis of C2-Symmetric gem-Difluoromethylenated Angular Triquinanes." Journal of Organic Chemistry 83, no. 1 (2017): 388–402. http://dx.doi.org/10.1021/acs.joc.7b02777.

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15

Allingham, Matthew T., Andrew Howard-Jones, Patrick J. Murphy, Dafydd A. Thomas, and Peter W. R. Caulkett. "Synthesis and applications of C2-symmetric guanidine bases." Tetrahedron Letters 44, no. 48 (2003): 8677–80. http://dx.doi.org/10.1016/j.tetlet.2003.09.162.

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16

Setsune, Jun-ichiro, Aki Tsukajima, and Junko Watanabe. "Synthesis and chiroptical property of C2-symmetric cyclohexapyrrole." Tetrahedron Letters 48, no. 9 (2007): 1531–35. http://dx.doi.org/10.1016/j.tetlet.2007.01.004.

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17

Kim, Hae-Jo, Dohyun Moon, Myoung Soo Lah, and Jong-In Hong. "Recognition of dihydroxynaphthalenes by a C2-symmetric host." Tetrahedron Letters 44, no. 9 (2003): 1887–90. http://dx.doi.org/10.1016/s0040-4039(03)00073-x.

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18

Peyman, Anusch, Karl-Heinz Budt, Jörg Spanig, Bernd Stowasser, and Dieter Ruppert. "C2-symmetric phosphinic acid inhibitors of HIV protease." Tetrahedron Letters 33, no. 32 (1992): 4549–52. http://dx.doi.org/10.1016/s0040-4039(00)61309-6.

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19

Allenmark, Stig, Urban Skogsberg, and Linda Thunberg. "Chiral selectors based on C2-symmetric dicarboxylic acids." Tetrahedron: Asymmetry 11, no. 17 (2000): 3527–34. http://dx.doi.org/10.1016/s0957-4166(00)00331-1.

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20

Delogu, Giovanna, Davide Fabbri, Maria Antonietta Dettori, Alessandra Forni, and Gianluigi Casalone. "C2-Symmetric sulfur derivatives of 2,2′,3,3′-tetramethoxybiphenyl." Tetrahedron: Asymmetry 12, no. 10 (2001): 1451–58. http://dx.doi.org/10.1016/s0957-4166(01)00247-6.

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21

Periasamy, Mariappan, Gurubrahamam Ramani, and Gopal Muthukumaragopal. "Convenient Methods for Synthesis of C2-Symmetric Diphenyltetrahydrothiophenes." Synthesis 2009, no. 10 (2009): e2-e2. http://dx.doi.org/10.1055/s-0029-1216797.

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22

Rao, Vutukuri Dharma, and Mariappan Periasamy. "Convenient Synthetic Methods to C2 Symmetric 3,4-Diphenylpyrrolidines." Synthesis 2000, no. 05 (2000): 703–6. http://dx.doi.org/10.1055/s-2000-6404.

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23

Bhowmick, Kartick C., and Navalkishore N. Joshi. "Syntheses and applications of C2-symmetric chiral diols." Tetrahedron: Asymmetry 17, no. 13 (2006): 1901–29. http://dx.doi.org/10.1016/j.tetasy.2006.06.023.

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24

Periasamy, Mariappan, Gurubrahamam Ramani, and Gopal Muthukumaragopal. "Convenient Methods for Synthesis of C2-Symmetric Diphenyltetrahydrothiophenes." Synthesis 2009, no. 10 (2009): 1739–43. http://dx.doi.org/10.1055/s-0028-1088123.

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25

Gumus, Melike, Ibrahim H. Giden, and Hamza Kurt. "Broadband self-collimation in C2 symmetric photonic crystals." Optics Letters 43, no. 11 (2018): 2555. http://dx.doi.org/10.1364/ol.43.002555.

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26

Freixa, Zoraida, Mark S. Beentjes, Guido D. Batema, et al. "SPANphos: A C2-Symmetric trans-Coordinating Diphosphane Ligand." Angewandte Chemie International Edition 42, no. 11 (2003): 1284–87. http://dx.doi.org/10.1002/anie.200390330.

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27

WALDMANN, H. "ChemInform Abstract: C2-Symmetric Amines as Chiral Auxiliaries." ChemInform 27, no. 51 (2010): no. http://dx.doi.org/10.1002/chin.199651311.

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28

Veselovsky, V. V., A. V. Lozanova, and E. A. Mistryukov. "ChemInform Abstract: Novel C2-Symmetric Bis-Oxazoline Ligands." ChemInform 45, no. 3 (2014): no. http://dx.doi.org/10.1002/chin.201403073.

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29

Kim, Sung-Ji, Kyoungyim Lee, Sang-sup Jew, Hyeung-geun Park, and Byeong-Seon Jeong. "C2-Symmetric Chiral Malonamides for Asymmetric Michael Reaction." Chemistry Letters 37, no. 4 (2008): 432–33. http://dx.doi.org/10.1246/cl.2008.432.

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30

Kempf, Dale J., Daniel W. Norbeck, LynnMarie Codacovi, et al. "Structure-based, C2 symmetric inhibitors of HIV protease." Journal of Medicinal Chemistry 33, no. 10 (1990): 2687–89. http://dx.doi.org/10.1021/jm00172a002.

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31

Bolm, Carsten, Oliver Simić, and Marc Martin. "C2-Symmetric Bissulfoximines in Palladium-catalyzed Allylic Alkylations." Synlett 2001, no. 12 (2001): 1878–80. http://dx.doi.org/10.1055/s-2001-18756.

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32

Opozda, Barbara. "Locally symmetric minimal affine Lagrangian surfaces in C2." Monatshefte für Mathematik 156, no. 4 (2008): 357–70. http://dx.doi.org/10.1007/s00605-008-0023-9.

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33

Vasilyev, Bizyaev, Komarov, Gatilov, and Tkachev. "Chiral C2-Symmetric Diimines with 4,5-Diazafluorene Units." Molecules 24, no. 17 (2019): 3186. http://dx.doi.org/10.3390/molecules24173186.

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Abstract:

A synthetic approach to a new group of stable chiral C2-symmetric diimines with the 4,5-diazafluorene core has been developed based on condensation of dipinodiazafluorene with aromatic diamines. The chemical structures of new compounds were proven by spectroscopic methods and X-ray crystallography. All the compounds form solvates with organic solvents (chloroform, benzene, 1,4-dioxane) and water. Specific spectral data of the new compounds are explained using calculated data (DFT). Diimines of the pinodiazafluorene series give colored reactions with transition metal ions and can be regarded as

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34

Bott, Simon G., Alan P. Marchand, and Zenghui Liu. "Structure of a C2-symmetric bis(benzyloxy)trishomocubanone." Journal of Chemical Crystallography 25, no. 11 (1995): 747–50. http://dx.doi.org/10.1007/bf01670329.

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35

Feng, Guo-Qiang, De-Xian Wang, Qi-Yu Zheng, and Mei-Xiang Wang. "Chemoenzymatic synthesis of enantiopure geminally dimethylated cyclopropane-based C2- and pseudo-C2-symmetric diamines." Tetrahedron: Asymmetry 17, no. 19 (2006): 2775–80. http://dx.doi.org/10.1016/j.tetasy.2006.10.030.

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36

Halterman, Ronald L., and Xiaodan Mei. "Synthesis of D2-symmetric 5,10,15,20-tetraarylporphyrins from C2-symmetric benzaldehydes and achiral aryldipyrromethanes." Tetrahedron Letters 37, no. 35 (1996): 6291–94. http://dx.doi.org/10.1016/0040-4039(96)01379-2.

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37

GURJAR, M. K., S. PAL, A. V. R. RAO, R. J. PARIZA, and M. S. CHORGHADE. "ChemInform Abstract: Synthesis of Novel C2-Symmetric and Pseudo C2-Symmetric Based Diols, Epoxides and Dideoxy Derivatives of HIV Protease Inhibitors." ChemInform 28, no. 34 (2010): no. http://dx.doi.org/10.1002/chin.199734093.

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38

Huynh, Khoi, Bryon K. Anderson, and Tom Livinghouse. "ChemInform Abstract: Enantioselective Hydroamination/Cyclization of Aminoalkenes by (Bis)-C2 Symmetric and (Mono)-C2 Symmetric Anionic Tetraamide Complexes of La(III)." ChemInform 46, no. 40 (2015): no. http://dx.doi.org/10.1002/chin.201540127.

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39

KEMPF, D. J., T. J. SOWIN, E. M. DOHERTY, et al. "ChemInform Abstract: Stereocontrolled Synthesis of C2-Symmetric and Pseudo-C2-Symmetric Diamino Alcohols and Diols for Use in HIV Protease Inhibitors." ChemInform 24, no. 7 (2010): no. http://dx.doi.org/10.1002/chin.199307101.

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40

Desimoni, Giovanni, Giuseppe Faita, and Karl Anker Jørgensen. "C2-Symmetric Chiral Bis(Oxazoline) Ligands in Asymmetric Catalysis." Chemical Reviews 106, no. 9 (2006): 3561–651. http://dx.doi.org/10.1021/cr0505324.

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41

Guo, Weicong, Qinzhe Liu, Jijun Jiang, and Jun Wang. "Development of a C2-Symmetric Chiral aza Spirocyclic Diol." Organic Letters 22, no. 8 (2020): 3110–13. http://dx.doi.org/10.1021/acs.orglett.0c00858.

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42

Görlitzer, Hans W., Michael Spiegler, and Reiner Anwander. "C2-symmetric bis(oxazolinato) complexes of yttrium and lanthanum † ‡." Journal of the Chemical Society, Dalton Transactions, no. 24 (1999): 4287–88. http://dx.doi.org/10.1039/a908313h.

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43

Rabouin, Daniel, Valérie Perron, Blaise N'Zemba, René C.-Gaudreault та Gervais Bérubé. "A facile synthesis of C2-symmetric 17β-estradiol dimers". Bioorganic & Medicinal Chemistry Letters 13, № 3 (2003): 557–60. http://dx.doi.org/10.1016/s0960-894x(02)00987-3.

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44

Graetz, Benjamin, Scott Rychnovsky, Wen-Hao Leu, Patrick Farmer, and Rong Lin. "C2-Symmetric nitroxides and their potential as enantioselective oxidants." Tetrahedron: Asymmetry 16, no. 21 (2005): 3584–98. http://dx.doi.org/10.1016/j.tetasy.2005.09.016.

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45

Seki, Masahiko, Toshiyuki Furutani, Masanori Hatsuda, and Ritsuo Imashiro. "Facile synthesis of C2-symmetric chiral binaphthyl ketone catalysts." Tetrahedron Letters 41, no. 13 (2000): 2149–52. http://dx.doi.org/10.1016/s0040-4039(00)00120-9.

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46

Hayashi, T., and G. Berthon-Gelloz. "Expanding the C2-Symmetric Bicyclo[2.2.1]heptadiene Ligand Family." Synfacts 2007, no. 2 (2007): 0179. http://dx.doi.org/10.1055/s-2006-955846.

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47

Behlen, Michael J., and Christopher Uyeda. "C2-Symmetric Dinickel Catalysts for Enantioselective [4 + 1]-Cycloadditions." Journal of the American Chemical Society 142, no. 41 (2020): 17294–300. http://dx.doi.org/10.1021/jacs.0c08262.

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48

TANNER, D., and C. BIRGERSSON. "ChemInform Abstract: C2-Symmetric Aziridines as Efficient Chiral Auxiliaries." ChemInform 23, no. 12 (2010): no. http://dx.doi.org/10.1002/chin.199212146.

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49

Pragliola, Stefania, Elio Forlenza, and Pasquale Longo. "C2-Symmetric Zirconocenes in the Polymerization of Conjugated Diolefins." Macromolecular Rapid Communications 22, no. 10 (2001): 783–86. http://dx.doi.org/10.1002/1521-3927(20010701)22:10<783::aid-marc783>3.0.co;2-d.

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50

Locke, Andrew J., Tom E. Pickett, and Christopher J. Richards. "ChemInform Abstract: Diastereoselective Synthesis of Enantiopure C2-Symmetric Dihaloferrocenes." ChemInform 32, no. 19 (2001): no. http://dx.doi.org/10.1002/chin.200119153.

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