Crafting mono- and novel bis-methylated pyrroloquinoxaline derivatives from a shared precursor and its application in the total synthesis of marinoquinoline A
The synthesis of mono- and novel bis-methylated pyrrolo[1,2-a]quinoxalines through the addition of unstable methyl radicals to aryl isocyanides is described contingent upon the reaction conditions employed. The strategy has been effectively employed in the total synthesis of the natural product mari...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
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Royal Society of Chemistry
2023
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Online Access: | https://repository.londonmet.ac.uk/8814/1/d3ra05952a.pdf |
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author | Damai, Margarita Guzzardi, Norman Lewis, Viliyana Rao, Zenobia X. Sykes, Daniel Patel, Bhaven |
author_facet | Damai, Margarita Guzzardi, Norman Lewis, Viliyana Rao, Zenobia X. Sykes, Daniel Patel, Bhaven |
author_sort | Damai, Margarita |
collection | LMU |
description | The synthesis of mono- and novel bis-methylated pyrrolo[1,2-a]quinoxalines through the addition of unstable methyl radicals to aryl isocyanides is described contingent upon the reaction conditions employed. The strategy has been effectively employed in the total synthesis of the natural product marinoquinoline A. |
first_indexed | 2024-07-09T04:07:11Z |
format | Article |
id | oai:repository.londonmet.ac.uk:8814 |
institution | London Metropolitan University |
language | English |
last_indexed | 2024-07-09T04:07:11Z |
publishDate | 2023 |
publisher | Royal Society of Chemistry |
record_format | eprints |
spelling | oai:repository.londonmet.ac.uk:88142023-10-30T15:16:10Z http://repository.londonmet.ac.uk/8814/ Crafting mono- and novel bis-methylated pyrroloquinoxaline derivatives from a shared precursor and its application in the total synthesis of marinoquinoline A Damai, Margarita Guzzardi, Norman Lewis, Viliyana Rao, Zenobia X. Sykes, Daniel Patel, Bhaven 540 Chemistry & allied sciences The synthesis of mono- and novel bis-methylated pyrrolo[1,2-a]quinoxalines through the addition of unstable methyl radicals to aryl isocyanides is described contingent upon the reaction conditions employed. The strategy has been effectively employed in the total synthesis of the natural product marinoquinoline A. Royal Society of Chemistry 2023-10-10 Article PeerReviewed text en cc_by_nc https://repository.londonmet.ac.uk/8814/1/d3ra05952a.pdf Damai, Margarita, Guzzardi, Norman, Lewis, Viliyana, Rao, Zenobia X., Sykes, Daniel and Patel, Bhaven (2023) Crafting mono- and novel bis-methylated pyrroloquinoxaline derivatives from a shared precursor and its application in the total synthesis of marinoquinoline A. RSC Advances, 13 (42). pp. 29561-29567. ISSN 2046-2069 https://pubs.rsc.org/en/content/articlelanding/2023/ra/d3ra05952a 10.1039/D3RA05952A |
spellingShingle | 540 Chemistry & allied sciences Damai, Margarita Guzzardi, Norman Lewis, Viliyana Rao, Zenobia X. Sykes, Daniel Patel, Bhaven Crafting mono- and novel bis-methylated pyrroloquinoxaline derivatives from a shared precursor and its application in the total synthesis of marinoquinoline A |
title | Crafting mono- and novel bis-methylated pyrroloquinoxaline derivatives from a shared precursor and its application in the total synthesis of marinoquinoline A |
title_full | Crafting mono- and novel bis-methylated pyrroloquinoxaline derivatives from a shared precursor and its application in the total synthesis of marinoquinoline A |
title_fullStr | Crafting mono- and novel bis-methylated pyrroloquinoxaline derivatives from a shared precursor and its application in the total synthesis of marinoquinoline A |
title_full_unstemmed | Crafting mono- and novel bis-methylated pyrroloquinoxaline derivatives from a shared precursor and its application in the total synthesis of marinoquinoline A |
title_short | Crafting mono- and novel bis-methylated pyrroloquinoxaline derivatives from a shared precursor and its application in the total synthesis of marinoquinoline A |
title_sort | crafting mono and novel bis methylated pyrroloquinoxaline derivatives from a shared precursor and its application in the total synthesis of marinoquinoline a |
topic | 540 Chemistry & allied sciences |
url | https://repository.londonmet.ac.uk/8814/1/d3ra05952a.pdf |
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