Synthetic Photochemistry. XXXVIII. The Photorearrangement of the Tropone Endoperoxide, 6,7-Dioxabicyclo[3.2.2]nona-3,8-dien-2-one
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/60/8/60_8_3037/_pdf
Reference9 articles.
1. Novel photochemical rearrangement of aryl-6,7-dioxabicyclo[3.2.2]nona-3,8-dien-2-one into tricyclic lactone
2. Stereoselectivity of Diels–Alder Reactions of 6,7-Dioxabicyclo[3.2.2]nona-3,8-dien-2-one and 6,7-Diethoxycarbonyl-6,7-diazabicyclo[3.2.2]nona-3,8-dien-2-one
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Two-Carbon Homologation of Aldehydes via Silyl Ketene Acetals: A New Stereoselective Approach to (E)-Alkenoic Acids;The Journal of Organic Chemistry;1998-11-01
2. Photochemistry of some 2,5-substituted tropone mesogens;Journal of Photochemistry and Photobiology A: Chemistry;1998-08
3. ChemInform Abstract: Synthetic Photochemistry. Part 38. The Photorearrangement of the Tropone Endoperoxide, 6,7-Dioxabicyclo(3.2.2)nona-3,8-dien-2-one (I).;ChemInform;1987-12-15
4. Synthetic Photochemistry. XXXIX. Sensitized-Photooxygenation of 2-Benzyltropone, 2-[Hydroxy(4-nitrophenyl)methyl]tropone, and 2-(1-Hydroxy-2-oxo-2-phenylethyl)tropone. A Quenching Effect of Hydroxyl Group in the Vicinity of the Reaction Site;Bulletin of the Chemical Society of Japan;1987-10
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