| Title: | Allene Synthesis from 2-Alkyn-1-Ols |
| Author: |
Kuo, Elaine Y.; Finney, Nathaniel S.; Myers, Andrew
Note: Order does not necessarily reflect citation order of authors. |
| Citation: | Myers, Andrew G., Nathaniel S. Finney, and Elaine Y. Kuo. 1989. Allene synthesis from 2-alkyn-1-Ols. Tetrahedron Letters 30(42): 5747-5750. |
| Access Status: | At the direction of the depositing author this work is not currently accessible through DASH. |
| Full Text & Related Files: |
myers13.pdf (264.0Kb; PDF)
|
| Abstract: | Activation of 2-alkyn-1-01s as their methanesulfonate esters and displacement with hydrazine urnishes the corresponding alkynyl hydrazine derivatives which undergo smooth oxidative rearrangement with diethyl azodicarboxylate (DEAD) or 4-methyl-1,2,4-triazoline-3,5-dione (MTAD) to form allenes. |
| Published Version: | http://dx.doi.org/10.1016/S0040-4039(00)76187-9 |
| Other Sources: | http://www.chem.harvard.edu/groups/myers/pdf_publications/tetlet_1989_30_5747.pdf |
| Citable link to this page: | http://nrs.harvard.edu/urn-3:HUL.InstRepos:3122543 |
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