Difference between revisions of "Template:Did you know nominations/Apparicine"
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imported>Cwmhiraeth (Passed for DYK) |
imported>Mifter (Promote to prep 2) |
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| − | + | <noinclude>[[Category:Passed DYK nominations from January 2017]]<div style="background-color: #F3F9FF; margin: 2em 0 0 0; padding: 0 10px 0 10px; border: 1px solid #AAAAAA;"> | |
| − | + | :''The following is an archived discussion of the DYK nomination of the article below. <span style="color:red">'''Please do not modify this page.'''</span> Subsequent comments should be made on the appropriate discussion page (such as [[{{TALKPAGENAME}}|this nomination's talk page]], [[Talk:{{SUBPAGENAME}}|the article's talk page]] or [[Wikipedia talk:Did you know]]), unless there is consensus to re-open the discussion at this page. '''No further edits should be made to this page'''.'' | |
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| − | | | + | The result was: '''promoted''' by [[User:Mifter|Mifter]] ([[User talk:Mifter|talk]]) 20:12, 12 February 2017 (UTC)<br /> |
{{DYK conditions}} | {{DYK conditions}} | ||
====Apparicine==== | ====Apparicine==== | ||
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{{main page image|image=Apparicine.svg|caption=The chemical structure of apparicine|width=120x133}} | {{main page image|image=Apparicine.svg|caption=The chemical structure of apparicine|width=120x133}} | ||
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* ... that establishing the structure of '''[[apparicine]]''' was a notable early use of [[nuclear magnetic resonance decoupling]] to determine a chemical structure? <small>{{cite encyclopedia|encyclopedia=The Chemistry of Heterocyclic Compound|title=Indoles: Part Four: The Monoterpenoid Indole Alkaloids|editor-last=Saxton|editor-first=J. Edwin|volume=25|publisher=[[John Wiley & Sons]]|year=1983|isbn=0470188448}}, page 287</small> | * ... that establishing the structure of '''[[apparicine]]''' was a notable early use of [[nuclear magnetic resonance decoupling]] to determine a chemical structure? <small>{{cite encyclopedia|encyclopedia=The Chemistry of Heterocyclic Compound|title=Indoles: Part Four: The Monoterpenoid Indole Alkaloids|editor-last=Saxton|editor-first=J. Edwin|volume=25|publisher=[[John Wiley & Sons]]|year=1983|isbn=0470188448}}, page 287</small> | ||
** '''ALT1''':... that the chemical structure of '''[[apparicine]]''' was established by [[nuclear magnetic resonance decoupling]] using the <sup>1</sup>H isotope of hydrogen? <small>{{cite book|title=Indole and Biogenetically Related Alkaloids|editor-last1=Phillipson|editor-first1=John David|editor-last2=Zenk|editor-first2=M.H.|others=Phytochemical Society of Europe|volume=17|series=Annual proceedings of the Phytochemical Society of Europe|publisher=Academic Press|year=1980|isbn=0125544502|issn=0309-9393}}, page 230</small> | ** '''ALT1''':... that the chemical structure of '''[[apparicine]]''' was established by [[nuclear magnetic resonance decoupling]] using the <sup>1</sup>H isotope of hydrogen? <small>{{cite book|title=Indole and Biogenetically Related Alkaloids|editor-last1=Phillipson|editor-first1=John David|editor-last2=Zenk|editor-first2=M.H.|others=Phytochemical Society of Europe|volume=17|series=Annual proceedings of the Phytochemical Society of Europe|publisher=Academic Press|year=1980|isbn=0125544502|issn=0309-9393}}, page 230</small> | ||
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:* ''Reviewed'': [[Template:Did you know nominations/The Transactor]] (see my [[User:Mindmatrix/Did you know|DYK tracker]]) | :* ''Reviewed'': [[Template:Did you know nominations/The Transactor]] (see my [[User:Mindmatrix/Did you know|DYK tracker]]) | ||
<small>Created by [[User:Mindmatrix|Mindmatrix]] ([[User talk:Mindmatrix|talk]]). Self-nominated at 17:18, 1 January 2017 (UTC).</small> | <small>Created by [[User:Mindmatrix|Mindmatrix]] ([[User talk:Mindmatrix|talk]]). Self-nominated at 17:18, 1 January 2017 (UTC).</small> | ||
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:* [[File:Symbol voting keep.svg|16px]] This article is new enough and long enough. The image is in the public domain and any of the hooks could be used, although I like ALT0 best. The article is neutral and neither Earwig nor I detected any policy issues. [[User:Cwmhiraeth|Cwmhiraeth]] ([[User talk:Cwmhiraeth|talk]]) 20:22, 7 February 2017 (UTC) | :* [[File:Symbol voting keep.svg|16px]] This article is new enough and long enough. The image is in the public domain and any of the hooks could be used, although I like ALT0 best. The article is neutral and neither Earwig nor I detected any policy issues. [[User:Cwmhiraeth|Cwmhiraeth]] ([[User talk:Cwmhiraeth|talk]]) 20:22, 7 February 2017 (UTC) | ||
| − | {{-}} | + | {{-}}</div></noinclude><!--Please do not write below this line or remove this line. Place comments above this line.--> |
Latest revision as of 20:12, 12 February 2017
- The following is an archived discussion of the DYK nomination of the article below. Please do not modify this page. Subsequent comments should be made on the appropriate discussion page (such as this nomination's talk page, the article's talk page or Wikipedia talk:Did you know), unless there is consensus to re-open the discussion at this page. No further edits should be made to this page.
The result was: promoted by Mifter (talk) 20:12, 12 February 2017 (UTC)
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Apparicine
- ... that establishing the structure of apparicine was a notable early use of nuclear magnetic resonance decoupling to determine a chemical structure? Saxton, J. Edwin, ed. (1983). "Indoles: Part Four: The Monoterpenoid Indole Alkaloids". The Chemistry of Heterocyclic Compound. 25. John Wiley & Sons. ISBN 0470188448., page 287
- ALT1:... that the chemical structure of apparicine was established by nuclear magnetic resonance decoupling using the 1H isotope of hydrogen? Phillipson, John David; Zenk, M.H., eds. (1980). Indole and Biogenetically Related Alkaloids. Annual proceedings of the Phytochemical Society of Europe. 17. Phytochemical Society of Europe. Academic Press. ISBN 0125544502. ISSN 0309-9393., page 230
- ALT2:... that the alkaloid apparicine has moderate to strong activity against some human pathogens? Schmelzer, G.H.; Gurib-Fakim, A., eds. (2008). Medicinal Plants. 1. PROTA Foundation, Backhuys Publishers. ISBN 9789057822049. ISSN 1877-430X., page 590
- ALT3:... that the alkaloid apparicine exhibits strong activity against poliovirus type 3? Schmelzer, G.H.; Gurib-Fakim, A., eds. (2008). Medicinal Plants. 1. PROTA Foundation, Backhuys Publishers. ISBN 9789057822049. ISSN 1877-430X., page 592
- ALT4:... that the alkaloid apparicine exhibits cytotoxicity against an experimental lymphocytic leukemia cell line? Schmelzer, G.H.; Gurib-Fakim, A., eds. (2008). Medicinal Plants. 1. PROTA Foundation, Backhuys Publishers. ISBN 9789057822049. ISSN 1877-430X., page 592
- Reviewed: Template:Did you know nominations/The Transactor (see my DYK tracker)
Created by Mindmatrix (talk). Self-nominated at 17:18, 1 January 2017 (UTC).
This article is new enough and long enough. The image is in the public domain and any of the hooks could be used, although I like ALT0 best. The article is neutral and neither Earwig nor I detected any policy issues. Cwmhiraeth (talk) 20:22, 7 February 2017 (UTC)