Photochemical behaviour of biased homo-conjugated ketones: details of an oxa-di-π-methane rearrangement-Reference-Cited by-同舟云学术

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Photochemical behaviour of biased homo-conjugated ketones: details of an oxa-di-π-methane rearrangement

Published:1982 Issue:24 Volume: Page:1375-1378
ISSN:0022-4936
Container-title:J. Chem. Soc., Chem. Commun.
language:en
Short-container-title:J. Chem. Soc., Chem. Commun.

Author:

Zizuashvili Jakob,Abramson Sarah,Shmueli Uri,Fuchs Benzion

Publisher

Royal Society of Chemistry (RSC)

Subject

Molecular Medicine

Link

http://pubs.rsc.org/en/content/articlepdf/1982/C3/C39820001375

Cited by 10 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. Applications of Di-Π-Methane and Related Rearrangement Reactions in Chemical Synthesis;Molecular Rearrangements in Organic Synthesis;2015-10-02

2. The Role of Spin−Orbit Coupling and Symmetry in Oxadi-π-methane Rearrangements and Some Related Photochemical Reactions;The Journal of Organic Chemistry;1996-01-01

3. Studies in the synthesis of polycyclopentanoids: synthesis, oxa-di-π-methane rearrangement of annulated bicyclo[2.2.2]octenones and cyclopropane ring cleavage of tetracyclo[6.3.0.0.0]undecenones;J. Chem. Soc., Perkin Trans. 1;1992

4. Oxa-di-π-methane Photoisomerizations;Comprehensive Organic Synthesis;1991

5. Structure of cis-tricyclo[6.3.0.02,8]undecane-3,11-dione;Acta Crystallographica Section C Crystal Structure Communications;1988-05-15

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