Base-catalyzed rearrangement of 3-bromobicyclo[3.2.1]octa-2,6-diene to endo-6-ethynylbicyclo[3.1.0]hex-2-ene. Possible intermediacy of a homoconjugated carbene-Reference-Cited by-同舟云学术

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Base-catalyzed rearrangement of 3-bromobicyclo[3.2.1]octa-2,6-diene to endo-6-ethynylbicyclo[3.1.0]hex-2-ene. Possible intermediacy of a homoconjugated carbene

Published:1970-04 Issue:7 Volume:92 Page:2163-2164
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Bergman Robert G.,Rajadhyaksha V. J.

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja00710a076

Cited by 25 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

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3. Alkenes from Tosylhydrazones;Organic Reactions;2011-03-15

4. The reaction of some polycyclic halides with lithium p,p′-di-tert-butylbiphenyl;Recueil des Travaux Chimiques des Pays-Bas;2010-09-02

5. Studies in the C8H8 field. Formation of Endo-6-ethynylbicyclo[3.1.0]hex-2-ene by gas-phase photolysis of a carbon suboxide/bicyclo[2.2.1]hepta-2,5-diene mixture: (Short Communication);Recueil des Travaux Chimiques des Pays-Bas;2010-09-02

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