The di-π-methane rearrangements of 1,4-dihydro-1,4-methano- and -ethanonaphthalene-5,8-diols
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Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1976/P1/P19760000550
Cited by 5 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. Effective control of regioselectivity by a bridgehead substituent in the di-.pi.-methane rearrangement of dibenzobarrelenes and benzonorbornadienes;Journal of the American Chemical Society;1984-10
2. Control of regioselectivity in the di-.pi.-methane rearrangements. Triplet-sensitized photoisomerization of benzonorbornadienes carrying cyano substituents in the aryl and vinyl segments;Journal of the American Chemical Society;1979-09
3. Photochemistry of bicyclic compounds. The di-.pi.-methane rearrangement of 5-methylene-2-norbornenes;The Journal of Organic Chemistry;1979-05
4. Control by meta substituents of benzo-vinyl bonding options during triplet sensitized photorearrangement of benzonorbornadienes and anti-7,8-benzotricyclo[4.2.2.02,5]deca-3,7,9-trienes;Journal of the American Chemical Society;1977-05
5. ChemInform Abstract: THE DI-Π-METHANE REARRANGEMENTS OF 1,4-DIHYDRO-1,4-METHANO- AND -ETHANONAPHTHALENE-5,8-DIOLS;Chemischer Informationsdienst;1976-05-25
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