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Total Synthesis and Prediction of Ulodione Natural Products Guided by DFT Calculations

A biomimetic synthetic strategy has resulted in a two‐step total synthesis of (±)‐ulodione A and the prediction of two potential natural products, (±)‐ulodiones C and D. This work was guided by computational investigations into the selectivity of a proposed biosynthetic Diels–Alder dimerization, whi...

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Autores principales: Bestwick, Jacob S., Jones, David J., Jones, Helen E., Kalomenopoulos, Panagiotis G., Szabla, Rafal, Lawrence, Andrew L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9401604/
https://www.ncbi.nlm.nih.gov/pubmed/35670364
http://dx.doi.org/10.1002/anie.202207004
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author Bestwick, Jacob S.
Jones, David J.
Jones, Helen E.
Kalomenopoulos, Panagiotis G.
Szabla, Rafal
Lawrence, Andrew L.
author_facet Bestwick, Jacob S.
Jones, David J.
Jones, Helen E.
Kalomenopoulos, Panagiotis G.
Szabla, Rafal
Lawrence, Andrew L.
author_sort Bestwick, Jacob S.
collection PubMed
description A biomimetic synthetic strategy has resulted in a two‐step total synthesis of (±)‐ulodione A and the prediction of two potential natural products, (±)‐ulodiones C and D. This work was guided by computational investigations into the selectivity of a proposed biosynthetic Diels–Alder dimerization, which was then utilized in the chemical synthesis. This work highlights how biosynthetic considerations can both guide the design of efficient synthetic strategies and lead to the anticipation of new natural products.
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spelling pubmed-94016042022-08-26 Total Synthesis and Prediction of Ulodione Natural Products Guided by DFT Calculations Bestwick, Jacob S. Jones, David J. Jones, Helen E. Kalomenopoulos, Panagiotis G. Szabla, Rafal Lawrence, Andrew L. Angew Chem Int Ed Engl Research Articles A biomimetic synthetic strategy has resulted in a two‐step total synthesis of (±)‐ulodione A and the prediction of two potential natural products, (±)‐ulodiones C and D. This work was guided by computational investigations into the selectivity of a proposed biosynthetic Diels–Alder dimerization, which was then utilized in the chemical synthesis. This work highlights how biosynthetic considerations can both guide the design of efficient synthetic strategies and lead to the anticipation of new natural products. John Wiley and Sons Inc. 2022-06-28 2022-08-08 /pmc/articles/PMC9401604/ /pubmed/35670364 http://dx.doi.org/10.1002/anie.202207004 Text en © 2022 The Authors. Angewandte Chemie International Edition published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) 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.
spellingShingle Research Articles
Bestwick, Jacob S.
Jones, David J.
Jones, Helen E.
Kalomenopoulos, Panagiotis G.
Szabla, Rafal
Lawrence, Andrew L.
Total Synthesis and Prediction of Ulodione Natural Products Guided by DFT Calculations
title Total Synthesis and Prediction of Ulodione Natural Products Guided by DFT Calculations
title_full Total Synthesis and Prediction of Ulodione Natural Products Guided by DFT Calculations
title_fullStr Total Synthesis and Prediction of Ulodione Natural Products Guided by DFT Calculations
title_full_unstemmed Total Synthesis and Prediction of Ulodione Natural Products Guided by DFT Calculations
title_short Total Synthesis and Prediction of Ulodione Natural Products Guided by DFT Calculations
title_sort total synthesis and prediction of ulodione natural products guided by dft calculations
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9401604/
https://www.ncbi.nlm.nih.gov/pubmed/35670364
http://dx.doi.org/10.1002/anie.202207004
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