CC bond cleavage in the interaction of anthraquinone triplet with tertiary alcohols and tertiary butylbenzene
✍ Scribed by G. Móger; M. Győr
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- French
- Weight
- 239 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
In the photochemical reaction of anthraquinone triplet with both tertiary alcohols and tert.Bu-benzene in C6H6 are also broken, yielding CH at A.2334 nm not only C-H (or O-H) bonds but C-C bonds 3' and R1C(R2)OH (or C6HSC(CH3)2)radicals, at room temperature. Wagner and Puchalski have shown, that in the photochemical interaction of acetophenone triplet (TRO) with I-phenylethanol (HROH) in C6H6 both a-CH and O-H bonds are broken, yielding alkoxy radicals, which may undergo 8-scission.' At the same time we have
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Replacement of the C-19 tertiary hydroxyl group of some thebdine and oripavine derivatives with bridged ring C (so-called Benfley's compounds) for an azido group has been performed with hydrazoic acid. In case the hydroxyl group was connected to a centre of chirality, substitution resulted in the fo