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Journal articles on the topic 'Bithiazol'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

M., N. JOSHI, S. BHAGWAT V., S. BHAGWAT V., and A. PARVATE J. "Synthesis of 3-[ 4" -Aryl-(2" -4' -bithiazol)-2' -yl]-2-aryl- 5-carboxymethyl-4-thiazolidinones and their Ester Derivatives." Journal of Indian Chemical Society Vol. 70, Jun 1993 (1993): 607–8. https://doi.org/10.5281/zenodo.5918084.

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Chemistry Department. Parle College, Dixit Road, Vile Parle (East), Bombay-400 057 <em>Manuscript received 4 December 1992, accepted 8 February 1993</em> Synthesis of 3-[ 4" -Aryl-(2" -4' -bithiazol)-2' -yl]-2-aryl- 5-carboxymethyl-4-thiazolidinones and their Ester Derivatives

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2

Filippone, Paolino, Stefania Santeusanio, Antonio Arcadi, Orazio Attanasi, Francesca Perrulli, and Elisabetta Rossi. "Efficient Synthesis of Novel Polyfunctionalised 4,5′-Bithiazol-4′-ol Derivatives." Synlett 2004, no. 15 (2004): 2681–84. http://dx.doi.org/10.1055/s-2004-835629.

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3

Just-Baringo, Xavier, Paolo Bruno, Fernando Albericio, and Mercedes Álvarez. "Highly efficient, multigram and enantiopure synthesis of (S)-2-(2,4′-bithiazol-2-yl)pyrrolidine." Tetrahedron Letters 52, no. 42 (2011): 5435–37. http://dx.doi.org/10.1016/j.tetlet.2011.07.128.

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4

Craig, DC, HA Goodwin, D. Onggo, and AD Rae. "Coordination of 2,2'-Bithiazole. Spectral, Magnetic and Structural Studies of the Iron(II) and Nickel(II) Complexes." Australian Journal of Chemistry 41, no. 11 (1988): 1625. http://dx.doi.org/10.1071/ch9881625.

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Iron(II) and nickel(II) complexes of 2,2′bithiazole (2bt) have been prepared. Salts of [Fe(2bt)3]2+ have spectral properties typical of iron(II) diimine systems. Their magnetic and Mossbauer spectral properties show an anomalous temperature-dependence which is associated with a temperature-induced singlet (1A1) ↔ quintet (5T2) transition. The manifestation of the spin transition is complicated by the existence of two modifications of the complex perchlorate. In one of these there is a relatively small fraction of quintet state species in an essentially low-spin lattice. This fraction increases

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5

Spanò, Virginia, Marilia Barreca, Vincenzo Cilibrasi, et al. "Evaluation of Fused Pyrrolothiazole Systems as Correctors of Mutant CFTR Protein." Molecules 26, no. 5 (2021): 1275. http://dx.doi.org/10.3390/molecules26051275.

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Cystic fibrosis (CF) is a genetic disease caused by mutations that impair the function of the CFTR chloride channel. The most frequent mutation, F508del, causes misfolding and premature degradation of CFTR protein. This defect can be overcome with pharmacological agents named “correctors”. So far, at least three different classes of correctors have been identified based on the additive/synergistic effects that are obtained when compounds of different classes are combined together. The development of class 2 correctors has lagged behind that of compounds belonging to the other classes. It was s

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6

Jenkins, Ieuan H., and Peter G. Pickup. "Electronically conducting polymers containing conjugated bithiazole moieties from bis(thienyl)bithiazoles." Macromolecules 26, no. 17 (1993): 4450–56. http://dx.doi.org/10.1021/ma00069a008.

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7

JOSHI, M. N., V. S. BHAGWAT, and J. A. PARVATE. "ChemInform Abstract: Synthesis of 3-(4′′-Aryl-(2′′-4′-bithiazol)-2′-yl)-2-aryl-5- carboxymethyl-4-thiazolidinones and Their Ester Derivatives." ChemInform 26, no. 1 (2010): no. http://dx.doi.org/10.1002/chin.199501155.

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8

Tsuno, Naoki, Akira Yukimasa, Osamu Yoshida, et al. "Discovery of novel 2′,4′-dimethyl-[4,5′-bithiazol]-2-yl amino derivatives as orally bioavailable TRPV4 antagonists for the treatment of pain: Part 1." Bioorganic & Medicinal Chemistry Letters 26, no. 20 (2016): 4930–35. http://dx.doi.org/10.1016/j.bmcl.2016.09.013.

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9

Tsuno, Naoki, Akira Yukimasa, Osamu Yoshida, et al. "Discovery of novel 2′,4′-dimethyl-[4,5′-bithiazol]-2-yl amino derivatives as orally bioavailable TRPV4 antagonists for the treatment of pain: Part 2." Bioorganic & Medicinal Chemistry Letters 26, no. 20 (2016): 4936–41. http://dx.doi.org/10.1016/j.bmcl.2016.09.014.

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10

Benali-Cherif, N., M. Pierrot, C. Baudrion, and J. P. Aune. "5,5'-Bithiazole and 2,5'-Bithiazole." Acta Crystallographica Section C Crystal Structure Communications 51, no. 1 (1995): 76–77. http://dx.doi.org/10.1107/s0108270194002969.

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11

Kalogirou, Andreas S., and Panayiotis A. Koutentis. "5,5′-Bis[9-(2-ethylhexyl)-9H-carbazol-3-yl]-4,4′-diphenyl-2,2′-bithiazole." Molbank 2024, no. 1 (2024): M1761. http://dx.doi.org/10.3390/m1761.

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Stille coupling between 5,5′-dibromo-4,4′-diphenyl-2,2′-bithiazole and 9-(2-ethylhexyl)-3-(tributylstannyl)-9H-carbazole in the presence of Pd(Ph3P)2Cl2 in toluene, heated at reflux for 2 h, gave 5,5′-bis[9-(2-ethylhexyl)-9H-carbazol-3-yl]-4,4′-diphenyl-2,2′-bithiazole in 85% yield.

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12

Guo, Jiali, Wei Tang, Yingshuang Zhang, et al. "Simple non-fused small-molecule acceptors with bithiazole core: synthesis, crystallinity and photovoltaic properties." Materials Advances 3, no. 1 (2022): 554–61. http://dx.doi.org/10.1039/d1ma00954k.

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13

Guo, Chang, Jesse Quinn, Bin Sun, and Yuning Li. "Dramatically different charge transport properties of bisthienyl diketopyrrolopyrrole-bithiazole copolymers synthesized via two direct (hetero)arylation polymerization routes." Polymer Chemistry 7, no. 27 (2016): 4515–24. http://dx.doi.org/10.1039/c6py00762g.

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Two diketopyrrolopyrrole-bithiazole copolymers with same building blocks synthesized via direct (hetero)arylation polymerization through different routes show dramatically different charge transport properties.

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14

Caron, Elise, Christopher M. Brown, Duane Hean, and Michael O. Wolf. "Variable oxidation state sulfur-bridged bithiazole ligands tune the electronic properties of ruthenium(ii) and copper(i) complexes." Dalton Transactions 48, no. 4 (2019): 1263–74. http://dx.doi.org/10.1039/c8dt04588g.

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15

Torabi, S. Ali Asghar, Fahimeh Jamali, George A. Koutsantonis, Ali Morsali, Brian W. Skelton, and Allan H. White. "4,4′-Bithiazoles as Ligands: Crystal and Molecular Structure of bis(O,O′-Nitrato)(2,2′-diphenyl-4,4′-bithiazole)copper(II) (Two Polymorphs)." Australian Journal of Chemistry 56, no. 9 (2003): 949. http://dx.doi.org/10.1071/ch03016.

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A low-temperature single-crystal X-ray structure determination of the 1 : 1 adduct of copper(II) nitrate with 2,2′-diphenyl-4,4′-bithiazole (L) shows it to be a molecular complex with L behaving as a symmetrical N,N′ chelate, and the nitrate groups as unsymmetrical O,O′ chelates: [LCu(O2NO)2]. Two polymorphs, both monoclinic P21/c, have been obtained from acetonitrile (‘α’) and methanol (‘β’), respectively, with one molecule, devoid of crystallographic symmetry, in the asymmetric unit of each structure. The copper environments are distorted planar four-coordinate, cis-N2CuO2 (Cu–N 2.011(1), 1.

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16

Zhang, Chen, Ji Zhang, Weixuan Zeng, et al. "Benzobisthiadiazole-alt-bithiazole copolymers with deep HOMO levels for good-performance field-effect transistors with air stability and a high on/off ratio." Polymer Chemistry 7, no. 16 (2016): 2808–14. http://dx.doi.org/10.1039/c6py00212a.

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17

Huo, Jingpei, Wanying Zou, Yubang Zhang, et al. "Correction: Facile preparation of bithiazole-based material for inkjet printed light-emitting electrochemical cell." RSC Advances 9, no. 33 (2019): 19142. http://dx.doi.org/10.1039/c9ra90049g.

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18

Huo, Jingpei, Wanying Zou, Yubang Zhang, and Weilan Chen. "Retraction: Facile preparation of bithiazole-based material for inkjet printed light-emitting electrochemical cell." RSC Advances 10, no. 21 (2020): 12598. http://dx.doi.org/10.1039/d0ra90026e.

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19

Pal, Amlan K., David B. Cordes, Alexandra M. Z. Slawin, et al. "Simple design to achieve red-to-near-infrared emissive cationic Ir(iii) emitters and their use in light emitting electrochemical cells." RSC Advances 7, no. 51 (2017): 31833–37. http://dx.doi.org/10.1039/c7ra06347d.

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20

Kurt, Adnan, Hacer Andan, and Murat Koca. "Synthesis and characterization of a new conjugated polymer containing bithiazole group and its thermal decomposition kinetics." Macedonian Journal of Chemistry and Chemical Engineering 39, no. 2 (2020): 227. http://dx.doi.org/10.20450/mjcce.2020.2025.

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A new conjugated polymer containing a bithiazole group is prepared by the polycondensation of 2,2'-diamino-4,4'-bithiazole and terephthaldialdehyde in the presence of glacial acetic acid. The kinetics of thermal degradation of the new polymer are investigated by thermogravimetric analysis at different heating rates. The temperature corresponding to the maximum rate loss shifts to higher temperatures with increasing heating rate. The thermal decomposition activation energies of the conjugated polymer in a conversion range of 3–15 % are 288.4 and 281.1 kJ/mol by the Flynn–Wall–Ozawa and Kissinge

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21

ZHANG, XIAOYU, FULING GUO, XIN LI, et al. "EFFECT OF THIOPHENE IN BITHIAZOLE-BRIDGED SENSITIZERS ON THE PERFORMANCE OF DYE-SENSITIZED SOLAR CELLS." Nano 09, no. 05 (2014): 1440009. http://dx.doi.org/10.1142/s1793292014400098.

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In this paper, we have designed and synthesized four bithiazole-bridged sensitizers (BT-T2, TBT-T2, BT-T3 and TBT-T3) with triphenylamine and indoline as the donor segment and applied them to dye-sensitized solar cells (DSSCs). For triphenylamine-based sensitizers as BT-T2 and TBT-T2, adding one thiophene unit between triphenylamine donor and bithiazole moiety not only led to bathochromic shift of the maximum absorption and increase of molar extinction coefficient, but also enhanced the photovoltaic conversion efficiency from 7.12% of BT-T2 to 7.51% of TBT-T2. But for indoline-based sensitizer

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22

Müller, Philipp, Benjamin Bucior, Giulia Tuci, et al. "Computational screening, synthesis and testing of metal–organic frameworks with a bithiazole linker for carbon dioxide capture and its green conversion into cyclic carbonates." Molecular Systems Design & Engineering 4, no. 5 (2019): 1000–1013. http://dx.doi.org/10.1039/c9me00062c.

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23

Lam, P. L., G. L. Lu, K. H. Choi, et al. "Antimicrobial and toxicological evaluations of binuclear mercury(ii)bis(alkynyl) complexes containing oligothiophenes and bithiazoles." RSC Advances 6, no. 20 (2016): 16736–44. http://dx.doi.org/10.1039/c5ra27600d.

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We investigated the antimicrobial activity of bis-(alkynyl)mercury(ii) complexes with oligothiophene and bithiazole linking units against MRSA and C. albicans, and their cytotoxicity was tested on NIH 3T3 cells.

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24

Huo, Jingpei, Wanying Zou, Yubang Zhang, et al. "Retracted Article: Facile preparation of bithiazole-based material for inkjet printed light-emitting electrochemical cell." RSC Advances 9, no. 11 (2019): 6163–68. http://dx.doi.org/10.1039/c9ra00093c.

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Light-emitting electrochemical cell of bithiazole-based material was fabricated by solution processing rendered high external quantum efficiency over 12.8% and luminance of 1.8 10<sup>4</sup> cd m<sup>−2.</sup>

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25

Benali-Cherif, N., M. Pierrot, C. Baudrion, and J. P. Aune. "2,4'-Bithiazole and Bis(2,4'-bithiazole)bis(dimethyl sulfoxide)copper(II) Diperchlorate." Acta Crystallographica Section C Crystal Structure Communications 51, no. 1 (1995): 72–75. http://dx.doi.org/10.1107/s0108270194002970.

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26

Mercuri, Giorgio, Marco Moroni, Simona Galli, et al. "UiO-67-derived bithiophene and bithiazole MIXMOFs for luminescence sensing and removal of contaminants of emerging concern in wastewater." Inorganic Chemistry Frontiers 9, no. 1 (2022): 90–102. http://dx.doi.org/10.1039/d1qi01184g.

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The UiO-67-type MIXMOF [Zr6O4(OH)4(PhPh)5(TzTz)], containing a blue-emitting bithiazole linker, is a potential multifunctional material for environmental remediation, being both a luminescent sensor and an adsorbent for diclofenac in aqueous solutions.

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27

V., S. BHAGWAT, A. PARVATE J., and N. JOSHI M. "Synthesis of 2''-Azetidinones bearing 2,4'-Bithiazole Moiety as Possible Antibacterials." Journal of Indian Chemical Society Vol. 69, Apr 1992 (1992): 231–32. https://doi.org/10.5281/zenodo.6089972.

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Chemistry Department, Parle College, Dixit Road, Vile Parle (East), Bombay-400 057 <em>Manuscript received 90 January 1992, accepted 23 March 1992</em> Synthesis of 2<em>''</em>-Azetidinones bearing 2,4'-Bithiazole Moiety as Possible Antibacterials.

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28

Oniwa, Kazuaki, Hiromasa Kikuchi, Thangavel Kanagasekaran, et al. "Biphenyl end-capped bithiazole co-oligomers for high performance organic thin film field effect transistors." Chemical Communications 52, no. 27 (2016): 4926–29. http://dx.doi.org/10.1039/c6cc01352j.

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Two new regiospecific biphenyl end-capped bithiazole co-oligomers, BP2Tz(in) and BP2Tz(out), showed high hole mobilities of 3.5 and 0.4 cm<sup>2</sup> V<sup>−1</sup> s<sup>−1</sup>, respectively, in thin film field effect transistors.

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29

V., S. BHAGWAT, A. PARVATE J., and N. JOSHI M. "Synthesis of Schiff Bases and Thiazolidinones bearing 2,4'-Bithiazole Moiety." Journal of Indian Chemical Society Vol. 68, Jul 1991 (1991): 419–20. https://doi.org/10.5281/zenodo.6158687.

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Chemistry Department, Parle College, Dixit Road, Vile Parle ( East ), Bombay-4.00 057 <em>Manuscript received 19 January 1990, revised 14 January 1991, accepted 11 July 1991</em> Synthesis of Schiff Bases and Thiazolidinones bearing 2,4'-Bithiazole Moiety.

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30

Lassalas, Pierrik, Christophe Berini, Jean-Baptiste E. Y. Rouchet, et al. "Miyaura borylation/Suzuki–Miyaura coupling (MBSC) sequence of 4-bromo-2,4′-bithiazoles with halides: straightforward access to a heterocylic cluster of d-series of thiopeptide GE2270." Organic & Biomolecular Chemistry 16, no. 4 (2018): 526–30. http://dx.doi.org/10.1039/c7ob02866k.

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31

Feng, Yijun, Jincheng Zhang, Yongbing Pei, Qiu Chen, Yue Yan, and Lianbin Wu. "A Novel Strategy to Tune Magnetic Properties of Nickel(II)-Schiff Base Coordination Bridged Polysilsesquioxane." Science of Advanced Materials 11, no. 12 (2019): 1705–11. http://dx.doi.org/10.1166/sam.2019.3600.

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In this paper, liquid state solvent-free organosilica-based nickel-bithiazole complexes (PBSIBTHM-Ni2+, PBSIBTMeM-Ni2+) were synthesized through sol–gel processes respectively, and these two metal complexes and their precursors were characterized. The precursors with bithiazole were successfully prepared, their inorganic and organic parts were connected on molecular level. The DSC results indicated they would all exist in liquid phase at temperature ranging from 180 K to 280 K. The UV-VIS showed that a red shift of the main electronic transitions from 254 to 268 nm of PBSIBTHM to PBSIBTHM-Ni2+

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32

Bolognesi, A., M. Catellani, S. Destri, and W. Porzio. "Structure of 4,4'-dimethyl-2,2'-bithiazole." Acta Crystallographica Section C Crystal Structure Communications 43, no. 6 (1987): 1171–73. http://dx.doi.org/10.1107/s0108270187092631.

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33

Preston, J., and W. B. Black. "Thermally stable amide-bithiazole ordered copolymers." Journal of Polymer Science Part C: Polymer Symposia 23, no. 1 (2007): 441–48. http://dx.doi.org/10.1002/polc.5070230152.

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34

Trigo-López, Miriam, Ana M. Sanjuán, Aranzazu Mendía, Asunción Muñoz, Félix C. García, and José M. García. "Heteroaromatic Polyamides with Improved Thermal and Mechanical Properties." Polymers 12, no. 8 (2020): 1793. http://dx.doi.org/10.3390/polym12081793.

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We prepared high-performance aromatic copolyamides, containing bithiazole and thiazolo-thiazole groups in their main chain, from aromatic diamines and isophthaloyl chloride, to further improve the prominent thermal behavior and exceptional mechanical properties of commercial aramid fibers. The introduction of these groups leads to aramids with improved strength and moduli compared to commercial meta-oriented aromatic polyamides, together with an increase of their thermal performance. Moreover, their solubility, water uptake, and optical properties were evaluated in this work.

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35

Houssin, Raymond, Nicole Helbecque, Jean-Luc Bernier, and Jean-Pierre H[etilde]nichart. "A New Bithiazole Derivative with Intercalative Properties." Journal of Biomolecular Structure and Dynamics 4, no. 2 (1986): 219–29. http://dx.doi.org/10.1080/07391102.1986.10506341.

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36

MacLean, Brian J., and Peter G. Pickup. "Electron Transport in Bithiophene−Bithiazole Based Metallopolymers." Journal of Physical Chemistry B 106, no. 24 (2002): 6354. http://dx.doi.org/10.1021/jp021167c.

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37

Park, Jong-Wook, Ji-Hoon Lee, Sam-Il Kho, and Tae Wan Kim. "Synthesis and luminescent properties of bithiazole derivatives." Current Applied Physics 1, no. 2-3 (2001): 125–27. http://dx.doi.org/10.1016/s1567-1739(01)00003-7.

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38

MacLean, Brian J., and Peter G. Pickup. "Electron Transport in Bithiophene−Bithiazole Based Metallopolymers." Journal of Physical Chemistry B 106, no. 18 (2002): 4658–62. http://dx.doi.org/10.1021/jp0141934.

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39

MacLean, Brian J., and Peter G. Pickup. "Bithiophene–bithiazole copolymers and their metal complexes." Journal of Materials Chemistry 11, no. 5 (2001): 1357–63. http://dx.doi.org/10.1039/b009568k.

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40

Ahn, Jong-Woong, Kyoung Hwa Jang, Hyeong-Cheol Yang, Ki-Bong Oh, Hyi-Seung Lee, and Jongheon Shin. "Bithiazole Metabolites from the Myxobacterium Myxococcus fulvus." CHEMICAL & PHARMACEUTICAL BULLETIN 55, no. 3 (2007): 477–79. http://dx.doi.org/10.1248/cpb.55.477.

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41

Findlater, Michael, Nicholas S. Swisher, and Peter S. White. "Synthesis and Structure of Boron-Bithiazole Complexes." European Journal of Inorganic Chemistry 2010, no. 34 (2010): 5379–82. http://dx.doi.org/10.1002/ejic.201000940.

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42

Abedini, Jafar, and Ali Morsali. "Syntheses and Characterization of Two New 4,4’-Bithiazole d10 Complexes, Structural Characterization of M(DABTZ)2(CH3COO)](ClO4) · 2H2O (M = Zn, Cd)." Zeitschrift für Naturforschung B 60, no. 9 (2005): 951–54. http://dx.doi.org/10.1515/znb-2005-0907.

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New zinc(II) and cadmium(II) complexes of the 2,2’-diamino-4,4’-bithiazole (DABTZ) ligand, [M(DABTZ)2(CH3COO)](ClO4), have been synthesized and characterized by elemental analysis, IR, 1H NMR and 13C NMR spectroscopy. The structural characterization of the Cd(DABTZ)2(CH3COO)](ClO4) · 2H2O complex shows the complex to be a monomer and the Cd atom to be coordinated by four nitrogen atoms of the “DABTZ” ligands and two oxygen atoms of the acetate anion. There is an edge-to-edge π-π stacking interaction between the parallel aromatic rings.

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43

Mahjoub, A. R., and A. Morsali. "Crystal structure of 2,2'-diphenyl-4,4'-bithiazole, C18H12N2S2." Zeitschrift für Kristallographie - New Crystal Structures 218, no. 1 (2003): 121–22. http://dx.doi.org/10.1524/ncrs.2003.218.1.121.

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44

Mahjoub, A. R., and A. Morsali. "Crystal structure of 2,2′-diphenyl-4,4-bithiazole,C18H12N2S2." Zeitschrift für Kristallographie - New Crystal Structures 218, JG (2003): 121–22. http://dx.doi.org/10.1524/ncrs.2003.218.jg.121.

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45

Imbach, J. L., G. Gosselin, D. Mrani, et al. "Synthesis and properties of bithiazole-linked netropsin derivatives." Antiviral Research 15 (April 1991): 59. http://dx.doi.org/10.1016/0166-3542(91)90114-7.

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46

Mohamed, Adel A. "Conformations and rotational barriers of 2,2?-bithiazole and 4,4?-dimethyl-2,2?-bithiazole semiemperical, ab initio, and density functional theory calculations." International Journal of Quantum Chemistry 79, no. 6 (2000): 367–77. http://dx.doi.org/10.1002/1097-461x(2000)79:6<367::aid-qua5>3.0.co;2-1.

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47

Saito, Isao, Takashi Morii, Yukihisa Okumura, Satoru Mori, Kizashi Yamaguchi, and Teruo Matsuura. "Ring-selective photorearrangement of bithiazoles." Tetrahedron Letters 27, no. 52 (1986): 6385–88. http://dx.doi.org/10.1016/s0040-4039(00)87815-6.

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48

Krause, Kirsten, Ronald A. Krause, and Susan Lamtruong. "Copper(I) Complexes of Bithiazoles." Journal of Coordination Chemistry 19, no. 1-3 (1988): 91–99. http://dx.doi.org/10.1080/00958972.1988.9728147.

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49

Dekkers, Johanna F., Ricardo A. Gogorza Gondra, Evelien Kruisselbrink, et al. "Optimal correction of distinct CFTR folding mutants in rectal cystic fibrosis organoids." European Respiratory Journal 48, no. 2 (2016): 451–58. http://dx.doi.org/10.1183/13993003.01192-2015.

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Small-molecule therapies that restore defects in cystic fibrosis transmembrane conductance regulator (CFTR) gating (potentiators) or trafficking (correctors) are being developed for cystic fibrosis (CF) in a mutation-specific fashion. Options for pharmacological correction of CFTR-p.Phe508del (F508del) are being extensively studied but correction of other trafficking mutants that may also benefit from corrector treatment remains largely unknown.We studied correction of the folding mutants CFTR-p.Phe508del, -p.Ala455Glu (A455E) and -p.Asn1303Lys (N1303K) by VX-809 and 18 other correctors (C1–C1

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50

Cowden, WB, SJ Sullivan, and DJ Brown. "Unfused Heterobicycles as Amplifiers of Phleomycin. VII> Some Bithiazoles; Thienyl-, Furanyl- and Thiazolyl-thiadiazoles and Related Oxadiazoles." Australian Journal of Chemistry 38, no. 8 (1985): 1257. http://dx.doi.org/10.1071/ch9851257.

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Syntheses are described for several unfused heterobicycles including 4,5′- and 2,4′-bithiazoles, 5-(thiazol-4′ and 5′-yl)-1,3,4- thiadiazoles , 5-(thien-2′-yl)-, 5-(furan-2′ and 3′-yl)-, thiadiazoles and related oxadiazoles, all with side chains containing dialkylamine terminal groups. The activities of these compounds as amplifiers of phleomycin -G are reported.

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