https://wiki.unissula.ac.id/index.php?action=history&feed=atom&title=Alkaloid_10-Hidroksi_Lycopodium 2026-09-16T14:05:19Z Riwayat revisi halaman ini di wiki MediaWiki 1.46.0 https://wiki.unissula.ac.id/index.php?title=Alkaloid_10-Hidroksi_Lycopodium&diff=29293&oldid=prev 2026-08-30T04:16:38Z

<p>Presentation V4: sitasi, referensi, Math, Wikimedia Commons, dan atribusi</p> <table style="background-color: #fff; color: #202122;" data-mw-interface=""> <col class="diff-marker" /> <col class="diff-content" /> <col class="diff-marker" /> <col class="diff-content" /> <tr class="diff-title" lang="id"> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Revisi sebelumnya</td> <td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revisi per 30 Agustus 2026 04.16</td> </tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l1">Baris 1:</td> <td colspan="2" class="diff-lineno">Baris 1:</td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">'''Alkaloid </del>10-<del style="font-weight: bold; text-decoration: none;">hidroksi ''Lycopodium''''', yang meliputi </del>10-<del style="font-weight: bold; text-decoration: none;">hidroksilikopodina, deasetilpanikulina, dan panikulina, adalah serangkaian [[produk alami]] yang diisolasi dari tumbuhan [[Lycopodiopsida|paku</del>]] <del style="font-weight: bold; text-decoration: none;">Chili ''Lycopodium confertum''. Deasetilpanikulina dan panikulina juga dapat diisolasi dari ''Lycopodium paniculatum''.</del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">[[File:</ins>10-<ins style="font-weight: bold; text-decoration: none;">hydroxy_lycopodium_alkaliods.PNG|thumb|right|280px|</ins>10-<ins style="font-weight: bold; text-decoration: none;">hydroxy lycopodium alkaliods</ins>]]</div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr> <tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">'''Alkaloid 10-hidroksi ''Lycopodium''''', yang meliputi 10-hidroksilikopodina, deasetilpanikulina, dan panikulina, adalah serangkaian [[produk alami]] yang diisolasi dari tumbuhan [[Lycopodiopsida|paku]] Chili ''Lycopodium confertum''. Deasetilpanikulina dan panikulina juga dapat diisolasi dari ''Lycopodium paniculatum''.&lt;ref&gt;Orlando M. Muñoz. ''High Resolution NMR Studies of Paniculine and Related ''Lycopodium'' Compounds''. ''Journal of Natural Products''. January 1990. Vol. 53 (1). hlm. 200–203. doi:10.1021/np50067a032.&lt;/ref&gt;</ins></div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>[[Alkaloid]] ''Lycopodium'' dianggap menarik karena aktivitas biologis dan karakteristik kerangkanya yang unik, tetapi, banyak senyawa dalam kelas ini belum dipelajari dengan baik.</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>[[Alkaloid]] ''Lycopodium'' dianggap menarik karena aktivitas biologis dan karakteristik kerangkanya yang unik,<ins style="font-weight: bold; text-decoration: none;">&lt;ref&gt;[http://stoltz.caltech.edu/litmtg/mechclub/2008/AHSC7_08.pdf Lycopodine and the Lycopodium Alkaloids]. dead link needs update&lt;/ref&gt; </ins>tetapi, banyak senyawa dalam kelas ini belum dipelajari dengan baik.<ins style="font-weight: bold; text-decoration: none;">&lt;ref&gt;Lycopodium Alkaloids: An Intramolecular Michael Reaction Approach |https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-0036-1588851&lt;/ref&gt;</ins></div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Sintesis ==</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Sintesis ==</div></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div> </div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>Sintesis enantioselektif pertama dari 10-hidroksilikopodina, deasetilpanikulina dan panikulina diterbitkan oleh Mrinmoy Saha dan Rich Carter pada tahun 2013. Dua langkah kunci penutupan cincin dicapai dengan reaksi organokatalitik Michael dan [[reaksi Mannich]] yang dikatalisis asam Lewis.<ins style="font-weight: bold; text-decoration: none;">&lt;ref&gt;Mrinmoy Saha. ''Toward a Unified Approach for the Lycopodines: Synthesis of 10-Hydroxylycopodine, Deacetylpaniculine, and Paniculine''. ''Organic Letters''. February 2013. Vol. 15 (4). hlm. 736–739. doi:10.1021/ol303272w.&lt;/ref&gt; </ins>Dampak dari stereokimia C10 pada penambahan reaksi Michael adalah untuk membangun ikatan C7-C12 dan pada siklisasi Mannich yang telah dieksplorasi baru-baru ini.<ins style="font-weight: bold; text-decoration: none;">&lt;ref&gt;Mrinmoy Saha. ''Unified Synthesis of 10-Oxygenated Lycopodium Alkaloids: Impact of C10-Stereochemistry on Reactivity''. ''J Org Chem''. June 2016. Vol. 81 (14). hlm. 5963–5980. doi:10.1021/acs.joc.6b00900.&lt;/ref&gt;</ins></div></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>Sintesis enantioselektif pertama dari 10-hidroksilikopodina, deasetilpanikulina dan panikulina diterbitkan oleh Mrinmoy Saha dan Rich Carter pada tahun 2013. Dua langkah kunci penutupan cincin dicapai dengan reaksi organokatalitik Michael dan [[reaksi Mannich]] yang dikatalisis asam Lewis. Dampak dari stereokimia C10 pada penambahan reaksi Michael adalah untuk membangun ikatan C7-C12 dan pada siklisasi Mannich yang telah dieksplorasi baru-baru ini.</div></td><td colspan="2" class="diff-side-added"></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Lihat juga ==</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Lihat juga ==</div></td></tr> <tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l13">Baris 13:</td> <td colspan="2" class="diff-lineno">Baris 13:</td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Referensi ==</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>== Referensi ==</div></td></tr> <tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">&lt;references /&gt;</ins></div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr> <tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">== Sumber dan atribusi ==</ins></div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr> <tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">Konten artikel ini diadaptasi dari [https://id.wikipedia.org/w/index.php?title=Alkaloid+10-Hidroksi+Lycopodium&amp;oldid=28472831 Wikipedia bahasa Indonesia], revisi 28472831 (2025-11-14T03:32:35Z), yang tersedia berdasarkan lisensi Creative Commons Atribusi-BerbagiSerupa (CC BY-SA). Gambar pada artikel ini bersumber dari Wikimedia Commons dan mengikuti ketentuan lisensi masing-masing berkas. Mohon gunakan konten dan media secara bijak serta sesuai dengan ketentuan lisensi yang berlaku.</ins></div></td></tr> <tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">== Sumber dan atribusi ==</del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">&lt;!</ins>-- <ins style="font-weight: bold; text-decoration: none;">WIKI_UNISSULA_PRESENTATION_V4 </ins>--<ins style="font-weight: bold; text-decoration: none;">&gt;</ins></div></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div> </div></td><td colspan="2" class="diff-side-added"></td></tr> <tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div><del style="font-weight: bold; text-decoration: none;">Konten artikel ini diadaptasi dari [https://id.wikipedia.org/w/index.php?title=Alkaloid+10</del>-<del style="font-weight: bold; text-decoration: none;">Hidroksi+Lycopodium&amp;oldid=28472831 Wikipedia bahasa Indonesia], revisi 28472831 (2025</del>-<del style="font-weight: bold; text-decoration: none;">11</del>-<del style="font-weight: bold; text-decoration: none;">14T03:32:35Z), yang tersedia berdasarkan lisensi Creative Commons Atribusi</del>-<del style="font-weight: bold; text-decoration: none;">BerbagiSerupa (CC BY-SA). Mohon gunakan konten ini secara bijak serta sesuai dengan ketentuan lisensi yang berlaku.</del></div></td><td colspan="2" class="diff-side-added"></td></tr> </table>

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<p>Impor teks terkontrol dari Wikipedia bahasa Indonesia; revisi 28472831; atribusi sumber disertakan.</p> <p><b>Halaman baru</b></p><div>&#039;&#039;&#039;Alkaloid 10-hidroksi &#039;&#039;Lycopodium&#039;&#039;&#039;&#039;&#039;, yang meliputi 10-hidroksilikopodina, deasetilpanikulina, dan panikulina, adalah serangkaian [[produk alami]] yang diisolasi dari tumbuhan [[Lycopodiopsida|paku]] Chili &#039;&#039;Lycopodium confertum&#039;&#039;. Deasetilpanikulina dan panikulina juga dapat diisolasi dari &#039;&#039;Lycopodium paniculatum&#039;&#039;.<br /> <br /> <br /> [[Alkaloid]] &#039;&#039;Lycopodium&#039;&#039; dianggap menarik karena aktivitas biologis dan karakteristik kerangkanya yang unik, tetapi, banyak senyawa dalam kelas ini belum dipelajari dengan baik.<br /> <br /> == Sintesis ==<br /> <br /> Sintesis enantioselektif pertama dari 10-hidroksilikopodina, deasetilpanikulina dan panikulina diterbitkan oleh Mrinmoy Saha dan Rich Carter pada tahun 2013. Dua langkah kunci penutupan cincin dicapai dengan reaksi organokatalitik Michael dan [[reaksi Mannich]] yang dikatalisis asam Lewis. Dampak dari stereokimia C10 pada penambahan reaksi Michael adalah untuk membangun ikatan C7-C12 dan pada siklisasi Mannich yang telah dieksplorasi baru-baru ini.<br /> <br /> == Lihat juga ==<br /> *[[Bubuk Lycopodium|Bubuk &#039;&#039;Lycopodium&#039;&#039;]]<br /> *&#039;&#039;[[Lycopodium clavatum]]&#039;&#039;<br /> <br /> == Referensi ==<br /> <br /> <br /> <br /> == Sumber dan atribusi ==<br /> <br /> Konten artikel ini diadaptasi dari [https://id.wikipedia.org/w/index.php?title=Alkaloid+10-Hidroksi+Lycopodium&amp;oldid=28472831 Wikipedia bahasa Indonesia], revisi 28472831 (2025-11-14T03:32:35Z), yang tersedia berdasarkan lisensi Creative Commons Atribusi-BerbagiSerupa (CC BY-SA). Mohon gunakan konten ini secara bijak serta sesuai dengan ketentuan lisensi yang berlaku.</div>

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