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An efficient 1,3-dipolar cycloaddition between aromatic selenoaldehydes and nitrile oxides or nitrile imines: an easy access to selenium-containing five-membered heterocyclic ring system
| Content Provider | Semantic Scholar |
|---|---|
| Author | Segi, Masahito Tanno, Katsuhiko Kojima, Masumi Honda, Mitsunori Nakajima, Tadashi |
| Copyright Year | 2007 |
| Abstract | Abstract 1,3-Dipolar cycloaddition between aromatic selenoaldehydes, generated by thermal retro Diels–Alder reaction of anthracene cycloadducts, and nitrile oxides or nitrile imines proceeded efficiently to give the corresponding [3+2] cycloadducts as a single isomer in good yields, being 1,4,2-oxaselenazoles or 1,3,4-selenadiazoles, respectively. |
| Starting Page | 2303 |
| Ending Page | 2306 |
| Page Count | 4 |
| File Format | PDF HTM / HTML |
| DOI | 10.1016/j.tetlet.2007.01.153 |
| Volume Number | 48 |
| Alternate Webpage(s) | https://kanazawa-u.repo.nii.ac.jp/?action=repository_action_common_download&item_id=7390&item_no=1&attribute_id=26&file_no=1 |
| Alternate Webpage(s) | https://doi.org/10.1016/j.tetlet.2007.01.153 |
| Language | English |
| Access Restriction | Open |
| Content Type | Text |
| Resource Type | Article |
