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Methods of Lysergic Acid Synthesis—The Key Ergot Alkaloid

Ergot is the spore form of the fungus Claviceps purpurea. Ergot alkaloids are indole compounds that are biosynthetically derived from L-tryptophan and represent the largest group of fungal nitrogen metabolites found in nature. The common part of ergot alkaloids is lysergic acid. This review shows th...

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Autores principales: Jastrzębski, Michał K., Kaczor, Agnieszka A., Wróbel, Tomasz M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9654825/
https://www.ncbi.nlm.nih.gov/pubmed/36364148
http://dx.doi.org/10.3390/molecules27217322
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author Jastrzębski, Michał K.
Kaczor, Agnieszka A.
Wróbel, Tomasz M.
author_facet Jastrzębski, Michał K.
Kaczor, Agnieszka A.
Wróbel, Tomasz M.
author_sort Jastrzębski, Michał K.
collection PubMed
description Ergot is the spore form of the fungus Claviceps purpurea. Ergot alkaloids are indole compounds that are biosynthetically derived from L-tryptophan and represent the largest group of fungal nitrogen metabolites found in nature. The common part of ergot alkaloids is lysergic acid. This review shows the importance of lysergic acid as a representative of ergot alkaloids. The subject of ergot and its alkaloids is presented, with a particular focus on lysergic acid. All methods of total lysergic acid synthesis—through Woodward, Hendrickson, and Szantay intermediates and Heck coupling methods—are presented. The topic of biosynthesis is also discussed.
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spelling pubmed-96548252022-11-15 Methods of Lysergic Acid Synthesis—The Key Ergot Alkaloid Jastrzębski, Michał K. Kaczor, Agnieszka A. Wróbel, Tomasz M. Molecules Review Ergot is the spore form of the fungus Claviceps purpurea. Ergot alkaloids are indole compounds that are biosynthetically derived from L-tryptophan and represent the largest group of fungal nitrogen metabolites found in nature. The common part of ergot alkaloids is lysergic acid. This review shows the importance of lysergic acid as a representative of ergot alkaloids. The subject of ergot and its alkaloids is presented, with a particular focus on lysergic acid. All methods of total lysergic acid synthesis—through Woodward, Hendrickson, and Szantay intermediates and Heck coupling methods—are presented. The topic of biosynthesis is also discussed. MDPI 2022-10-28 /pmc/articles/PMC9654825/ /pubmed/36364148 http://dx.doi.org/10.3390/molecules27217322 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Jastrzębski, Michał K.
Kaczor, Agnieszka A.
Wróbel, Tomasz M.
Methods of Lysergic Acid Synthesis—The Key Ergot Alkaloid
title Methods of Lysergic Acid Synthesis—The Key Ergot Alkaloid
title_full Methods of Lysergic Acid Synthesis—The Key Ergot Alkaloid
title_fullStr Methods of Lysergic Acid Synthesis—The Key Ergot Alkaloid
title_full_unstemmed Methods of Lysergic Acid Synthesis—The Key Ergot Alkaloid
title_short Methods of Lysergic Acid Synthesis—The Key Ergot Alkaloid
title_sort methods of lysergic acid synthesis—the key ergot alkaloid
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9654825/
https://www.ncbi.nlm.nih.gov/pubmed/36364148
http://dx.doi.org/10.3390/molecules27217322
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