| Autor: |
Mishra, Uttam K., Patel, Kaushalendra, Ramasastry, S. S. V. |
| Zdroj: |
Organic Letters; December 2018, Vol. 21 Issue: 1 p175-179, 5p |
| Abstrakt: |
A series of unexpected reactions triggered by the dimethyloxosulfonium methylide led to the discovery of unconventional approaches for the synthesis of cyclopropa-fused tetralones and indeno-spirocyclopropanes. These highly functionalized structures were further elaborated in one step to privileged scaffolds such as tetralones, indenones, and fluorenones. As a whole, the results presented herein establish new diversity-oriented folding pathways. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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