It is well known that S-ketoesters assume both ketonic and enolic structures by tautomerization and such keto-enol equilibria have hitherto been observed in a number of cyclic and acyclic enolizable 8-ketoesters. 1 However, most compounds reported so far exist only as an equilibrium mixture of the k
โฆ LIBER โฆ
Conformational preference in 8-alkyl-8, 9,10, 11-tetrahydro-7H-cycloocta[dedenaphthalene-9-ones
โ Scribed by Toshihiro Kamada; Osamu Yamamoto
- Book ID
- 104243843
- Publisher
- Elsevier Science
- Year
- 1977
- Tongue
- French
- Weight
- 240 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
Compared to cycloalkanes, little is known about the stereochemistry of pericyclic naphthalenes , particularly compounds of medium-sized rings. l-4 During our studies of conformations of the peri-ring system 394 in some derivatives of
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