Recently, Cargill and coworkers1 have reported that irradiation of antitricyclo[5.2.0.0 285]nona-3,8-dien-9-one(I)l'2 in methylenechloride with "black-CI, lights" gives homocubane as a major product. However, it may be expected that
✦ LIBER ✦
Die photoisomerisierung von 3,6-hexanooxepin-4,5-dicarbonsäureestern zu tricyclo[6.2.1.0 1,5] undec-9-en-(3a,6-methanooctahydroazulen)-derivaten
✍ Scribed by Axel Sczostak; Frank Sönnichsen; Werner Tochtermann; Eva-Maria Peters; Karl Peters; Hans Georg von Schnering
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- French
- Weight
- 210 KB
- Volume
- 26
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
Irradiation of the 3,6-hexanooxepins fs -& affords the tricycle 6.2.1.01'5 c 3 undec-9-ene(3a,6-methanooctahydroazulene)derivatives 2~ -& in about 50% yield.
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