Intramolecular cyclopropanation-ring fragmentation leading to spirocyclic ring construction: a stereoselective synthesis of .beta.-chamigrene-Reference-Cited by-同舟云学术

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Intramolecular cyclopropanation-ring fragmentation leading to spirocyclic ring construction: a stereoselective synthesis of .beta.-chamigrene

Published:1991-07 Issue:14 Volume:56 Page:4494-4498
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Adams Julian,Lepine-Frenette Carole,Spero Denice M.

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo00014a032

Cited by 28 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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2. Sesquiterpenes in grapes and wines: Occurrence, biosynthesis, functionality, and influence of winemaking processes;Comprehensive Reviews in Food Science and Food Safety;2019-12-19

3. Erratum: Antonsen, S.; et al. Synthesis of Racemic β-Chamigrene, a Spiro[5.5]undecane Sequiterpene. Molecules 2014, 19, 20664–20670;Molecules;2018-03-20

4. Formation of Alkenes by Elimination;Comprehensive Organic Transformations;2018-02-28

5. Formation of Alkanes and Arenes by Ring-forming Reactions;Comprehensive Organic Transformations;2018-02-28

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