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3-Angles Under 3-Sphere Approach for Conformational Analysis of 2,6-Dideoxy-2,6-Imino-D-Talonic Acid

Received: 9 September 2026     Accepted: 27 September 2026     Published: 28 October 2026
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Abstract

Relationships between vicinal ϕ - dihedral θHnHn+1 - tetrahedral φCn angles [deg] under Hopf fibration and Lie algebra theories enable conformational analysis with VISION molecular models on conformational routes that might be followed by six membered ring, i.e. 4C1: 0H5, 0H1, 2H1, 2H3, 4H3, 4H5, 0S2, 3,0B, 3S1, B1,4, 5S1, 2,5B, 2S0, B3,0, 1S3, 1,4B, 1S5, B2,5 of 2,6-dideoxy-2,6-imino-D-talonic acid 1D. Six dihedral angles with cis-, trans-ee, trans-aa stereochemistry calculated from only one vicinal coupling constant 3JHH[Hz] and torus and invers of torus equations, represented on 3-Sphere, a hypersphere in 4D, are restricted by the stereochemistry of sugar, by the combination of dihedral angles along its shape, tetrahedral angles and at list by the distorted boat B or skew S of relaxed 4C1 or 1C4 chair conformations. Dihedral angles at anomeric position calculated from vicinal coupling constant are compared with angles calculated from carbon chemical shift with Euler - Conic manifold. On VISION molecular models are simulated first two conformations B0,3 and B0,3 as etalon, followed by introduction the calculated exocyclic dihedral angles: 1. from dihedral angles calculated only from vicinal coupling constant 3JHH[Hz]: S13 (B0,3), and B0,3 (S20), S31; 2. or from carbon chemical shift δ[ppm] and vicinal coupling constant3JHH[Hz]: S13, B0,3, S20 and S31.

Published in Science Journal of Chemistry (Volume 14, Issue 5)
DOI 10.11648/j.sjc.20261405.13
Page(s) 161-175
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2026. Published by Science Publishing Group

Keywords

3-Sphere, Hopf Fibration, Lie Algebra, Dihedral Angles, Tetrahedral Angles, Six Membered Ring, D-talonic Iminocyclitol

References
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[2] C.-I. Mitan, E. Bartha, C. Draghici, M. T. Caproiu, P. Filip, R. M. Moriarty, Hopf fibration on relationship between dihedral angle θHnHn+1[deg] and vicinal angle ϕ[deg], angles calculated from NMR data with 3-sphere approach and Java Script, Science Journal of Chemistry 2022, 10, 21.
[3] C.-I. Mitan, E. Bartha, P. Filip, C. Draghici, M.-T. Caproiu, R. M. Moriarty, Java Script programs for calculation of dihedral angles with manifold equations, Science Journal of Chemistry 2024, 12(3), 42;
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[7] E. Bartha, C.-I. Mitan, P. Filip, 3-Sphere torsional angles and six Membered ring conformation, American Journal of Quantum Chemistry and Molecular Spectroscopy 2023, 7(1), 9;
[8] C.-I. Mitan, E. Bartha, F. Petru, C. Draghici, M.-T. Caproiu, R. M. Moriarty, Manifold inversion on prediction dihedral angle from vicinal coupling constant with 3-sphere approach, Rev. Roum. Chim. 2023, 68(3-4), 185;
[9] C. I. Mitan, E. Bartha, P. Filip, R. Moriarty, Nuclear Magnetic Resonance Spectroscopy - Recent Research and Applications, chapter book: Dihedral and tetrahedral angles of five and six membered ring calculated from NMR data with 3-Sphere approach, IntachOpen 2025 ISBN 978-1-83635-220-4;
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[13] C.-I. Mitan, E. Bartha, P. Filip, V. dragutan, I. dragutan, C. Deleanu, C. Draghici, M.-T. Caproiu, R. M. Moriarty, 3-Spherical conformation insights into iminocyclitols with 1-α-D-ribose and 1-β-L-ribose stereochemistry under homotopic behavior of nuclear magnetic resonance data, Science Jouranl of Chemistry 2026, 14(1), 1;
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Cite This Article
  • APA Style

    Mitan, C., Bartha, E., Filip, P. (2026). 3-Angles Under 3-Sphere Approach for Conformational Analysis of 2,6-Dideoxy-2,6-Imino-D-Talonic Acid. Science Journal of Chemistry, 14(5), 161-175. https://doi.org/10.11648/j.sjc.20261405.13

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    ACS Style

    Mitan, C.; Bartha, E.; Filip, P. 3-Angles Under 3-Sphere Approach for Conformational Analysis of 2,6-Dideoxy-2,6-Imino-D-Talonic Acid. Sci. J. Chem. 2026, 14(5), 161-175. doi: 10.11648/j.sjc.20261405.13

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    AMA Style

    Mitan C, Bartha E, Filip P. 3-Angles Under 3-Sphere Approach for Conformational Analysis of 2,6-Dideoxy-2,6-Imino-D-Talonic Acid. Sci J Chem. 2026;14(5):161-175. doi: 10.11648/j.sjc.20261405.13

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  • @article{10.11648/j.sjc.20261405.13,
      author = {Carmen-Irena Mitan and Emerich Bartha and Petru Filip},
      title = {3-Angles Under 3-Sphere Approach for Conformational Analysis of 2,6-Dideoxy-2,6-Imino-D-Talonic Acid},
      journal = {Science Journal of Chemistry},
      volume = {14},
      number = {5},
      pages = {161-175},
      doi = {10.11648/j.sjc.20261405.13},
      url = {https://doi.org/10.11648/j.sjc.20261405.13},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.sjc.20261405.13},
      abstract = {Relationships between vicinal ϕ - dihedral θHnHn+1 - tetrahedral φCn angles [deg] under Hopf fibration and Lie algebra theories enable conformational analysis with VISION molecular models on conformational routes that might be followed by six membered ring, i.e. 4C1: 0H5, 0H1, 2H1, 2H3, 4H3, 4H5, 0S2, 3,0B, 3S1, B1,4, 5S1, 2,5B, 2S0, B3,0, 1S3, 1,4B, 1S5, B2,5 of 2,6-dideoxy-2,6-imino-D-talonic acid 1D. Six dihedral angles with cis-, trans-ee, trans-aa stereochemistry calculated from only one vicinal coupling constant 3JHH[Hz] and torus and invers of torus equations, represented on 3-Sphere, a hypersphere in 4D, are restricted by the stereochemistry of sugar, by the combination of dihedral angles along its shape, tetrahedral angles and at list by the distorted boat B or skew S of relaxed 4C1 or 1C4 chair conformations. Dihedral angles at anomeric position calculated from vicinal coupling constant are compared with angles calculated from carbon chemical shift with Euler - Conic manifold. On VISION molecular models are simulated first two conformations B0,3 and B0,3 as etalon, followed by introduction the calculated exocyclic dihedral angles: 1. from dihedral angles calculated only from vicinal coupling constant 3JHH[Hz]: S13 (B0,3), and B0,3 (S20), S31; 2. or from carbon chemical shift δ[ppm] and vicinal coupling constant3JHH[Hz]: S13, B0,3, S20 and S31.},
     year = {2026}
    }
    

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  • TY  - JOUR
    T1  - 3-Angles Under 3-Sphere Approach for Conformational Analysis of 2,6-Dideoxy-2,6-Imino-D-Talonic Acid
    AU  - Carmen-Irena Mitan
    AU  - Emerich Bartha
    AU  - Petru Filip
    Y1  - 2026/10/28
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    N1  - https://doi.org/10.11648/j.sjc.20261405.13
    DO  - 10.11648/j.sjc.20261405.13
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    JF  - Science Journal of Chemistry
    JO  - Science Journal of Chemistry
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    PB  - Science Publishing Group
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    UR  - https://doi.org/10.11648/j.sjc.20261405.13
    AB  - Relationships between vicinal ϕ - dihedral θHnHn+1 - tetrahedral φCn angles [deg] under Hopf fibration and Lie algebra theories enable conformational analysis with VISION molecular models on conformational routes that might be followed by six membered ring, i.e. 4C1: 0H5, 0H1, 2H1, 2H3, 4H3, 4H5, 0S2, 3,0B, 3S1, B1,4, 5S1, 2,5B, 2S0, B3,0, 1S3, 1,4B, 1S5, B2,5 of 2,6-dideoxy-2,6-imino-D-talonic acid 1D. Six dihedral angles with cis-, trans-ee, trans-aa stereochemistry calculated from only one vicinal coupling constant 3JHH[Hz] and torus and invers of torus equations, represented on 3-Sphere, a hypersphere in 4D, are restricted by the stereochemistry of sugar, by the combination of dihedral angles along its shape, tetrahedral angles and at list by the distorted boat B or skew S of relaxed 4C1 or 1C4 chair conformations. Dihedral angles at anomeric position calculated from vicinal coupling constant are compared with angles calculated from carbon chemical shift with Euler - Conic manifold. On VISION molecular models are simulated first two conformations B0,3 and B0,3 as etalon, followed by introduction the calculated exocyclic dihedral angles: 1. from dihedral angles calculated only from vicinal coupling constant 3JHH[Hz]: S13 (B0,3), and B0,3 (S20), S31; 2. or from carbon chemical shift δ[ppm] and vicinal coupling constant3JHH[Hz]: S13, B0,3, S20 and S31.
    VL  - 14
    IS  - 5
    ER  - 

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Author Information
  • Department of Chemistry, Institute of Organic and Supramolecular Chemistry “Costin. D. Nenitescu”, Bucharest, Romania

  • Department of Chemistry, Institute of Organic and Supramolecular Chemistry “Costin. D. Nenitescu”, Bucharest, Romania

  • Department of Chemistry, Institute of Organic and Supramolecular Chemistry “Costin. D. Nenitescu”, Bucharest, Romania

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