## Abstract The synthesis of benzo[a]pyrene‐6‐^13^C is described. Perinaphthane was converted to 6‐benzoyl‐carbonyl‐^13^C‐perinaphthane which was cyclized to 2,3‐dihydrobenzo[a]pyren‐6(1H)‐one‐6‐^13^C. Subsequent reduction of the ketone followed by dehydration and dehydrogenation gave benzo[a]pyren
✦ LIBER ✦
EPR Studies of 13C-labeled and monomethylated 6-oxybenzo[α]pyrene and 6-trifluoroacetoxy-benzo[a]pyrene radicals
✍ Scribed by Xinhua Chen; Fouad Bannoura; Paul D Sullivan
- Publisher
- Elsevier Science
- Year
- 1987
- Weight
- 840 KB
- Volume
- 75
- Category
- Article
- ISSN
- 0022-2364
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