A recent report by Zwanenburg and Rlunder' concerning the synthesis and reactions of the bridgehead substituted homocubyl alcohol derivative, 1, prompts us to report our efforts to prepare some reactively functionalized 4,5-dieubstituted homocubyl derivatives, 2. These compound8 ware desired for a s
โฆ LIBER โฆ
Bis-homoketonization of some 4,5-disubstituted homocubyl derivatives
โ Scribed by R.D. Miller; D. Dolce
- Book ID
- 104246744
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- French
- Weight
- 206 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
There are presently a number of examples of homoketonization reported in the literature. 1
Our current interest in strained, unenolizable a-diketones led to the investigation of the pheno.
menon of bis-homoketonization of certain vicinal dials, where the alcohol functionality is situated at strained ring junctures, as potential synthetic sources of interesting s-diketones.
Our preliminary results on 4,5-dihydroxypentacyclo [4.3.0.02'5.03y8.04'7] nonane, l&, are described.in this communic.,.ion.
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