Reassignment of improbable natural products identified through chemical principle screening
Natural products continue to be reported at an astonishing rate from a wide range of multidisciplinary research activities in the pursuit of understanding the chemistry of biodiversity. However, the elucidation of chemical structure in the modern era is heavily reliant on the analysis and interpreta...
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sg-ntu-dr.10356-1703992023-09-11T15:34:34Z Reassignment of improbable natural products identified through chemical principle screening Elyashberg, Mikhail Novitskiy, Ivan M. Bates, Roderick Wayland Kutateladze, Andrei G. Williams, Craig M. School of Physical and Mathematical Sciences Science::Chemistry Computer-Assisted Structure Elucidation Natural Products Natural products continue to be reported at an astonishing rate from a wide range of multidisciplinary research activities in the pursuit of understanding the chemistry of biodiversity. However, the elucidation of chemical structure in the modern era is heavily reliant on the analysis and interpretation of multiple spectroscopic outputs, and in most cases this activity is by no means trivial. Structural errors continue to be described given the inherent complexity of natural products. Computer-Assisted Structure Elucidation (CASE) continues to provide improved resolving power in this regard, but for enhanced accuracy quantum chemical spectrum prediction methodology is paramount. Reported herein are a range of counterfactual natural products, identified through chemical principal screening, which have been reassigned using a combination of chemical intuition, chemical synthesis, CASE and DU8+ spectrum prediction. Nanyang Technological University Published version We thank the University of Denver, the University of Queensland and Nanyang Technological University for financial support, along with Advanced Chemistry Development, Inc. (ACDLabs). The Australian Research Council for funding to C.M.W. (FT110100851). A.G.K. thanks the US National Science Foundation (CHE‐1955892) for support. 2023-09-11T05:36:59Z 2023-09-11T05:36:59Z 2022 Journal Article Elyashberg, M., Novitskiy, I. M., Bates, R. W., Kutateladze, A. G. & Williams, C. M. (2022). Reassignment of improbable natural products identified through chemical principle screening. European Journal of Organic Chemistry, 2022(34), e202200572-. https://dx.doi.org/10.1002/ejoc.202200572 1434-193X https://hdl.handle.net/10356/170399 10.1002/ejoc.202200572 2-s2.0-85133977902 34 2022 e202200572 en European Journal of Organic Chemistry © 2022 The Authors. European Journal of Organic Chemistry published by Wiley-VCH GmbH. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. application/pdf |
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Science::Chemistry Computer-Assisted Structure Elucidation Natural Products Elyashberg, Mikhail Novitskiy, Ivan M. Bates, Roderick Wayland Kutateladze, Andrei G. Williams, Craig M. Reassignment of improbable natural products identified through chemical principle screening |
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Natural products continue to be reported at an astonishing rate from a wide range of multidisciplinary research activities in the pursuit of understanding the chemistry of biodiversity. However, the elucidation of chemical structure in the modern era is heavily reliant on the analysis and interpretation of multiple spectroscopic outputs, and in most cases this activity is by no means trivial. Structural errors continue to be described given the inherent complexity of natural products. Computer-Assisted Structure Elucidation (CASE) continues to provide improved resolving power in this regard, but for enhanced accuracy quantum chemical spectrum prediction methodology is paramount. Reported herein are a range of counterfactual natural products, identified through chemical principal screening, which have been reassigned using a combination of chemical intuition, chemical synthesis, CASE and DU8+ spectrum prediction. |
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School of Physical and Mathematical Sciences |
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School of Physical and Mathematical Sciences Elyashberg, Mikhail Novitskiy, Ivan M. Bates, Roderick Wayland Kutateladze, Andrei G. Williams, Craig M. |
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Article |
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Elyashberg, Mikhail Novitskiy, Ivan M. Bates, Roderick Wayland Kutateladze, Andrei G. Williams, Craig M. |
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Elyashberg, Mikhail |
title |
Reassignment of improbable natural products identified through chemical principle screening |
title_short |
Reassignment of improbable natural products identified through chemical principle screening |
title_full |
Reassignment of improbable natural products identified through chemical principle screening |
title_fullStr |
Reassignment of improbable natural products identified through chemical principle screening |
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Reassignment of improbable natural products identified through chemical principle screening |
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reassignment of improbable natural products identified through chemical principle screening |
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2023 |
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https://hdl.handle.net/10356/170399 |
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