Synthesis of the tetracyclic core of the neomangicols using a late-stage indene alkylation
A general approach to the tetracyclic core of the neomangicol natural products via a late-stage indene alkylation reaction is presented. This strategy sets the stage for access to the neomangicol family and, in addition, provides a potential biogenetically inspired entry to the mangicol natural products.
| Medienart: |
E-Artikel |
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| Erscheinungsjahr: |
2009 |
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| Erschienen: |
2009 |
| Enthalten in: |
Zur Gesamtaufnahme - volume:11 |
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| Enthalten in: |
Organic letters - 11(2009), 14 vom: 16. Juli, Seite 3128-31 |
| Sprache: |
Englisch |
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| Beteiligte Personen: |
Wood, Jessica L [VerfasserIn] |
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| Links: |
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| Themen: |
67H8Y6LB8A |
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| Anmerkungen: |
Date Completed 13.08.2009 Date Revised 20.10.2021 published: Print Citation Status MEDLINE |
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| doi: |
10.1021/ol9010008 |
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| funding: |
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| Förderinstitution / Projekttitel: |
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| PPN (Katalog-ID): |
NLM189292369 |
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| 245 | 1 | 0 | |a Synthesis of the tetracyclic core of the neomangicols using a late-stage indene alkylation |
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| 500 | |a published: Print | ||
| 500 | |a Citation Status MEDLINE | ||
| 520 | |a A general approach to the tetracyclic core of the neomangicol natural products via a late-stage indene alkylation reaction is presented. This strategy sets the stage for access to the neomangicol family and, in addition, provides a potential biogenetically inspired entry to the mangicol natural products | ||
| 650 | 4 | |a Journal Article | |
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| 650 | 4 | |a Research Support, Non-U.S. Gov't | |
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| 700 | 1 | |a Sarpong, Richmond |e verfasserin |4 aut | |
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