Regioselective photoacylation of substituted naphthoquinones
Schiel, C., Oelgemoeller, M., and Mattay, J. (1998) Regioselective photoacylation of substituted naphthoquinones. Journal of Information Recording, 24. pp. 257-260.
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Abstract
Photoreactions of aldehydes with quinones exhibit acylated hydroquinones in good yields. In the case of substituted naphthoquinones (pos. 5-8) two regioisomers are formed. However, lithium perchlorate as additive affords only one regioisomer. This effect is discussed on the basis of semiemperical calculations.
| Item ID: | 29903 |
|---|---|
| Item Type: | Article (Research - C1) |
| ISSN: | 1025-6008 |
| Date Deposited: | 28 Oct 2013 02:45 |
| FoR Codes: | 03 CHEMICAL SCIENCES > 0305 Organic Chemistry > 030503 Organic Chemical Synthesis @ 40% 03 CHEMICAL SCIENCES > 0305 Organic Chemistry > 030505 Physical Organic Chemistry @ 60% |
| SEO Codes: | 97 EXPANDING KNOWLEDGE > 970103 Expanding Knowledge in the Chemical Sciences @ 100% |
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