Treatment of 1-diazo-3-(2-thienyl)-2-propanone with catalytic rhodium (II) acetate results in cyclopropanation followed by acid-catalyzed ring opening and tautomerization to yield 5,6-dihydro-4Hcyclopenta[b]thiophen-5-one. Under the same conditions, however, the isomeric l-diazo-3-(3-thienyl)-2propa
โฆ LIBER โฆ
A novel ring expansion of 1-carboethoxy-1,1-trimethylene-3-diazo-2-propanone
โ Scribed by R.D Miller; W Theis
- Book ID
- 104218634
- Publisher
- Elsevier Science
- Year
- 1986
- Tongue
- French
- Weight
- 229 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
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