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Revision as of 15:48, 27 June 2011 editYikrazuul (talk | contribs)Rollbackers1,991 edits svg← Previous edit		Latest revision as of 21:36, 19 September 2024 edit undoAdventureRick (talk | contribs)13 editsm "attracted a lot of attention" reads very informal, changed to "attracted significant attention"
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	{{Chembox| verifiedrevid = 404899192		{{Chembox| verifiedrevid = 436518223
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	| ImageFile = Aspidophytine.svg		| ImageFile = Aspidophytine.svg
	| Section1 = {{Chembox Identifiers		| Section1 = {{Chembox Identifiers
			| CASNo_Ref = {{cascite|correct|??}}
	| CASNo =16625-21-1		| CASNo =16625-21-1
	| PubChem = 11783895		| PubChem = 11783895
	| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}		| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
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	'''Aspidophytine''' is an ] ] that has attracted a lot of attention from synthetic chemists.<ref>''"Enantioselective Total Synthesis of Aspidophytine"''&nbsp;&nbsp;He, F.; Bo, Y.; Altom, J. D.; Corey, E. J. ''J. Am. Chem. Soc.'' '''1999''', ''121(28)'', 6771–6772 ({{DOI|10.1021/ja9915201}})</ref><ref>''"Stereocontrolled total synthesis of (−)-aspidophytine"''&nbsp;&nbsp;Sumi, S.; Matsumoto, K.; Tokuyama, H.; Fukuyama, T. ''Tetrahedron'' '''2003''', ''59'', 8571–8587 ({{DOI|10.1016/j.tet.2003.09.005}})</ref><ref>''"Application of the Rh(II) Cyclization/Cycloaddition Cascade for the Total Synthesis of (±)-Aspidophytine"&nbsp;&nbsp;'' Mejia-Oneto, J. M., Padwa, A. ''Org. Lett.'' '''2006''', ''8'', 3275–3278 ({{DOI|10.1021/ol061137i}})</ref><ref>''"A Concise Asymmetric Total Synthesis of Aspidophytine"&nbsp;&nbsp;''Nicolaou, K. C., Dalby, S. M., Majumder, U. ''J. Am. Chem. Soc.'' '''2008''', ''130(45)'', 14942–14943 ({{DOI|10.1021/ja806176w}})</ref> An extract of the ], aspidophytine is an ] substance particularly effective against ]es.		'''Aspidophytine''' is an ] ] that has attracted significant attention from synthetic chemists.<ref>''"Enantioselective Total Synthesis of Aspidophytine"''&nbsp;&nbsp;He, F.; Bo, Y.; Altom, J. D.; Corey, E. J. ''J. Am. Chem. Soc.'' '''1999''', ''121(28)'', 6771–6772 ({{doi|10.1021/ja9915201}})</ref><ref>''"Stereocontrolled total synthesis of (−)-aspidophytine"''&nbsp;&nbsp;Sumi, S.; Matsumoto, K.; Tokuyama, H.; Fukuyama, T. ''Tetrahedron'' '''2003''', ''59'', 8571–8587 ({{doi|10.1016/j.tet.2003.09.005}})</ref><ref>''"Application of the Rh(II) Cyclization/Cycloaddition Cascade for the Total Synthesis of (±)-Aspidophytine"&nbsp;&nbsp;'' Mejia-Oneto, J. M., Padwa, A. ''Org. Lett.'' '''2006''', ''8'', 3275–3278 ({{doi|10.1021/ol061137i}})</ref><ref>''"A Concise Asymmetric Total Synthesis of Aspidophytine"&nbsp;&nbsp;''Nicolaou, K. C., Dalby, S. M., Majumder, U. ''J. Am. Chem. Soc.'' '''2008''', ''130(45)'', 14942–14943 ({{doi|10.1021/ja806176w}})</ref> An extract of the ], aspidophytine is an ] substance particularly effective against ]es. It is one of the two components of the ] '''haplophytine'''.<ref name=TotallySynthetic>, by Paul Docherty, at the ]; published October 9, 2009; retrieved October 3, 2014</ref>
			In his suicide note, Harvard doctoral student ] mentioned his stress in attempting to devise a synthetic pathway for the aspidophytine sub-unit of haplophytine as a contributing factor to his psychological breakdown.<ref name=LethalChemistry>, by Stephen S> Hall, in '']''; published November 29, 1998; retrieved October 3, 2014</ref>
	The suicide note of Harvard doctoral student ] refers specifically to his stress in trying to synthesize the molecule.
	==References==		== References ==
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