Polycyclic Furanobutenolide-Derived Cembranoid and Norcembranoid Natural Products: Biosynthetic Connections and Synthetic Efforts
The polycyclic furanobutenolide-derived cembranoid and norcembranoid natural products are a family of congested, stereochemically complex, and extensively oxygenated polycyclic diterpenes and norditerpenes. Although the elegant architectures and biological activity profiles of these natural products...
Gespeichert in:
Veröffentlicht in: | Chemical reviews 2017-06, Vol.117 (12), p.7878-7909 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 7909 |
---|---|
container_issue | 12 |
container_start_page | 7878 |
container_title | Chemical reviews |
container_volume | 117 |
creator | Craig, Robert A Stoltz, Brian M |
description | The polycyclic furanobutenolide-derived cembranoid and norcembranoid natural products are a family of congested, stereochemically complex, and extensively oxygenated polycyclic diterpenes and norditerpenes. Although the elegant architectures and biological activity profiles of these natural products have captured the attention of chemists since the isolation of the first members of the family in the 1990s, the de novo synthesis of only a single polycyclic furanobutenolide-derived cembranoid and norcembranoid has been accomplished. This article begins with a brief discussion of the proposed biosyntheses and biosynthetic connections among the polycyclic furanobutenolide-derived cembranoids and norcembranoids and then provides a comprehensive review of the synthetic efforts toward each member of the natural product family, including biomimetic, semisynthetic, and de novo synthetic strategies. This body of knowledge has been gathered to provide insight into the reactivity and constraints of these compact and highly oxygenated polycyclic structures, as well as to offer guidance for future synthetic endeavors. |
doi_str_mv | 10.1021/acs.chemrev.7b00083 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5497599</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1924262544</sourcerecordid><originalsourceid>FETCH-LOGICAL-a572t-113a2c8ca21ab645ae32e41f0a6522b51ee6bbff2c57e44badfd0412b88b7b1a3</originalsourceid><addsrcrecordid>eNqFksFu1DAQhi0EokvLEyChSFy4ZGs7duJwQIKlpUhVqVQ4W7YzYV0ldrGdlfbIm-Ow2y1wgJPlme__PeMZhF4QvCSYklNl4tKsYQywWTYaYyyqR2hBOMVlLVr8GC1yrC1pXfMj9CzG23zlnDZP0REVmWJELNCPaz9szdYM1hTnU1DO6ymB84PtoPwAwW6gK1Yw6jllu0K5rrjywTxErlTKuqG4Dr6bTIpvivfWx61La0jZdOWdA5Osd_GX-OaQOet7H1I8QU96NUR4vj-P0dfzsy-ri_Ly88dPq3eXpeINTSUhlaJGGEWJ0jXjCioKjPRY1ZxSzQlArXXfU8MbYEyrru9yi1QLoRtNVHWM3u587yY9QmfApVy2vAt2VGErvbLyz4yza_nNbyRnbcPbNhu83hsE_32CmORoo4FhUA78FCXFvBKtaDD5L0raeVp5SCyjr_5Cb_0UXP6JTFFGa8rZTFU7ygQfY4D-UDfBct4GmbdB7rdB7rchq17-3vJBcz_-DJzugFn98O4_LH8CWb7Hcg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1924262544</pqid></control><display><type>article</type><title>Polycyclic Furanobutenolide-Derived Cembranoid and Norcembranoid Natural Products: Biosynthetic Connections and Synthetic Efforts</title><source>MEDLINE</source><source>American Chemical Society Journals</source><creator>Craig, Robert A ; Stoltz, Brian M</creator><creatorcontrib>Craig, Robert A ; Stoltz, Brian M</creatorcontrib><description>The polycyclic furanobutenolide-derived cembranoid and norcembranoid natural products are a family of congested, stereochemically complex, and extensively oxygenated polycyclic diterpenes and norditerpenes. Although the elegant architectures and biological activity profiles of these natural products have captured the attention of chemists since the isolation of the first members of the family in the 1990s, the de novo synthesis of only a single polycyclic furanobutenolide-derived cembranoid and norcembranoid has been accomplished. This article begins with a brief discussion of the proposed biosyntheses and biosynthetic connections among the polycyclic furanobutenolide-derived cembranoids and norcembranoids and then provides a comprehensive review of the synthetic efforts toward each member of the natural product family, including biomimetic, semisynthetic, and de novo synthetic strategies. This body of knowledge has been gathered to provide insight into the reactivity and constraints of these compact and highly oxygenated polycyclic structures, as well as to offer guidance for future synthetic endeavors.</description><identifier>ISSN: 0009-2665</identifier><identifier>ISSN: 1520-6890</identifier><identifier>EISSN: 1520-6890</identifier><identifier>DOI: 10.1021/acs.chemrev.7b00083</identifier><identifier>PMID: 28520418</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>bioactive properties ; Biological activity ; Biological Products - chemistry ; Biological Products - metabolism ; Biomimetics ; Biosynthesis ; Chemists ; Diterpenes - chemistry ; Diterpenes - metabolism ; diterpenoids ; Humans ; Natural products ; Oxygen ; stereochemistry</subject><ispartof>Chemical reviews, 2017-06, Vol.117 (12), p.7878-7909</ispartof><rights>Copyright © 2017 American Chemical Society</rights><rights>Copyright American Chemical Society Jun 28, 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a572t-113a2c8ca21ab645ae32e41f0a6522b51ee6bbff2c57e44badfd0412b88b7b1a3</citedby><cites>FETCH-LOGICAL-a572t-113a2c8ca21ab645ae32e41f0a6522b51ee6bbff2c57e44badfd0412b88b7b1a3</cites><orcidid>0000-0001-9837-1528</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acs.chemrev.7b00083$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acs.chemrev.7b00083$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>230,314,776,780,881,2751,27055,27903,27904,56716,56766</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28520418$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Craig, Robert A</creatorcontrib><creatorcontrib>Stoltz, Brian M</creatorcontrib><title>Polycyclic Furanobutenolide-Derived Cembranoid and Norcembranoid Natural Products: Biosynthetic Connections and Synthetic Efforts</title><title>Chemical reviews</title><addtitle>Chem. Rev</addtitle><description>The polycyclic furanobutenolide-derived cembranoid and norcembranoid natural products are a family of congested, stereochemically complex, and extensively oxygenated polycyclic diterpenes and norditerpenes. Although the elegant architectures and biological activity profiles of these natural products have captured the attention of chemists since the isolation of the first members of the family in the 1990s, the de novo synthesis of only a single polycyclic furanobutenolide-derived cembranoid and norcembranoid has been accomplished. This article begins with a brief discussion of the proposed biosyntheses and biosynthetic connections among the polycyclic furanobutenolide-derived cembranoids and norcembranoids and then provides a comprehensive review of the synthetic efforts toward each member of the natural product family, including biomimetic, semisynthetic, and de novo synthetic strategies. This body of knowledge has been gathered to provide insight into the reactivity and constraints of these compact and highly oxygenated polycyclic structures, as well as to offer guidance for future synthetic endeavors.</description><subject>bioactive properties</subject><subject>Biological activity</subject><subject>Biological Products - chemistry</subject><subject>Biological Products - metabolism</subject><subject>Biomimetics</subject><subject>Biosynthesis</subject><subject>Chemists</subject><subject>Diterpenes - chemistry</subject><subject>Diterpenes - metabolism</subject><subject>diterpenoids</subject><subject>Humans</subject><subject>Natural products</subject><subject>Oxygen</subject><subject>stereochemistry</subject><issn>0009-2665</issn><issn>1520-6890</issn><issn>1520-6890</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFksFu1DAQhi0EokvLEyChSFy4ZGs7duJwQIKlpUhVqVQ4W7YzYV0ldrGdlfbIm-Ow2y1wgJPlme__PeMZhF4QvCSYklNl4tKsYQywWTYaYyyqR2hBOMVlLVr8GC1yrC1pXfMj9CzG23zlnDZP0REVmWJELNCPaz9szdYM1hTnU1DO6ymB84PtoPwAwW6gK1Yw6jllu0K5rrjywTxErlTKuqG4Dr6bTIpvivfWx61La0jZdOWdA5Osd_GX-OaQOet7H1I8QU96NUR4vj-P0dfzsy-ri_Ly88dPq3eXpeINTSUhlaJGGEWJ0jXjCioKjPRY1ZxSzQlArXXfU8MbYEyrru9yi1QLoRtNVHWM3u587yY9QmfApVy2vAt2VGErvbLyz4yza_nNbyRnbcPbNhu83hsE_32CmORoo4FhUA78FCXFvBKtaDD5L0raeVp5SCyjr_5Cb_0UXP6JTFFGa8rZTFU7ygQfY4D-UDfBct4GmbdB7rdB7rchq17-3vJBcz_-DJzugFn98O4_LH8CWb7Hcg</recordid><startdate>20170628</startdate><enddate>20170628</enddate><creator>Craig, Robert A</creator><creator>Stoltz, Brian M</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9837-1528</orcidid></search><sort><creationdate>20170628</creationdate><title>Polycyclic Furanobutenolide-Derived Cembranoid and Norcembranoid Natural Products: Biosynthetic Connections and Synthetic Efforts</title><author>Craig, Robert A ; Stoltz, Brian M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a572t-113a2c8ca21ab645ae32e41f0a6522b51ee6bbff2c57e44badfd0412b88b7b1a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>bioactive properties</topic><topic>Biological activity</topic><topic>Biological Products - chemistry</topic><topic>Biological Products - metabolism</topic><topic>Biomimetics</topic><topic>Biosynthesis</topic><topic>Chemists</topic><topic>Diterpenes - chemistry</topic><topic>Diterpenes - metabolism</topic><topic>diterpenoids</topic><topic>Humans</topic><topic>Natural products</topic><topic>Oxygen</topic><topic>stereochemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Craig, Robert A</creatorcontrib><creatorcontrib>Stoltz, Brian M</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Chemical reviews</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Craig, Robert A</au><au>Stoltz, Brian M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Polycyclic Furanobutenolide-Derived Cembranoid and Norcembranoid Natural Products: Biosynthetic Connections and Synthetic Efforts</atitle><jtitle>Chemical reviews</jtitle><addtitle>Chem. Rev</addtitle><date>2017-06-28</date><risdate>2017</risdate><volume>117</volume><issue>12</issue><spage>7878</spage><epage>7909</epage><pages>7878-7909</pages><issn>0009-2665</issn><issn>1520-6890</issn><eissn>1520-6890</eissn><abstract>The polycyclic furanobutenolide-derived cembranoid and norcembranoid natural products are a family of congested, stereochemically complex, and extensively oxygenated polycyclic diterpenes and norditerpenes. Although the elegant architectures and biological activity profiles of these natural products have captured the attention of chemists since the isolation of the first members of the family in the 1990s, the de novo synthesis of only a single polycyclic furanobutenolide-derived cembranoid and norcembranoid has been accomplished. This article begins with a brief discussion of the proposed biosyntheses and biosynthetic connections among the polycyclic furanobutenolide-derived cembranoids and norcembranoids and then provides a comprehensive review of the synthetic efforts toward each member of the natural product family, including biomimetic, semisynthetic, and de novo synthetic strategies. This body of knowledge has been gathered to provide insight into the reactivity and constraints of these compact and highly oxygenated polycyclic structures, as well as to offer guidance for future synthetic endeavors.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>28520418</pmid><doi>10.1021/acs.chemrev.7b00083</doi><tpages>32</tpages><orcidid>https://orcid.org/0000-0001-9837-1528</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0009-2665 |
ispartof | Chemical reviews, 2017-06, Vol.117 (12), p.7878-7909 |
issn | 0009-2665 1520-6890 1520-6890 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5497599 |
source | MEDLINE; American Chemical Society Journals |
subjects | bioactive properties Biological activity Biological Products - chemistry Biological Products - metabolism Biomimetics Biosynthesis Chemists Diterpenes - chemistry Diterpenes - metabolism diterpenoids Humans Natural products Oxygen stereochemistry |
title | Polycyclic Furanobutenolide-Derived Cembranoid and Norcembranoid Natural Products: Biosynthetic Connections and Synthetic Efforts |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-25T02%3A32%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Polycyclic%20Furanobutenolide-Derived%20Cembranoid%20and%20Norcembranoid%20Natural%20Products:%20Biosynthetic%20Connections%20and%20Synthetic%20Efforts&rft.jtitle=Chemical%20reviews&rft.au=Craig,%20Robert%20A&rft.date=2017-06-28&rft.volume=117&rft.issue=12&rft.spage=7878&rft.epage=7909&rft.pages=7878-7909&rft.issn=0009-2665&rft.eissn=1520-6890&rft_id=info:doi/10.1021/acs.chemrev.7b00083&rft_dat=%3Cproquest_pubme%3E1924262544%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1924262544&rft_id=info:pmid/28520418&rfr_iscdi=true |