Use of allene in 1,3-dipolar addition to a carbonyl ylide: syntheses of 3-hydroxy-cis-nemorensic acid and nemorensic acid
1,3-Dipolar addition of allene to the carbonyl ylide derived from 6-diazoheptane-2,5-dione is the key step in syntheses of 3-hydroxy-cis-nemorensic acid and nemorensic acid.
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| Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2004-04 (7), p.822-823 |
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| container_issue | 7 |
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| container_title | Chemical communications (Cambridge, England) |
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| creator | Hodgson, David M Le Strat, Frédéric |
| description | 1,3-Dipolar addition of allene to the carbonyl ylide derived from 6-diazoheptane-2,5-dione is the key step in syntheses of 3-hydroxy-cis-nemorensic acid and nemorensic acid. |
| doi_str_mv | 10.1039/b316908a |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 1359-7345 |
| ispartof | Chemical communications (Cambridge, England), 2004-04 (7), p.822-823 |
| issn | 1359-7345 1364-548X |
| language | eng |
| recordid | cdi_proquest_miscellaneous_71763586 |
| source | Royal Society of Chemistry Journals Archive (1841-2007); MEDLINE; Royal Society Of Chemistry Journals 2008-; Alma/SFX Local Collection |
| subjects | Alkadienes - chemistry Azo Compounds - chemistry Furans - chemical synthesis Heptanes - chemistry Models, Chemical Pyrrolizidine Alkaloids - chemical synthesis Stereoisomerism |
| title | Use of allene in 1,3-dipolar addition to a carbonyl ylide: syntheses of 3-hydroxy-cis-nemorensic acid and nemorensic acid |
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