Selective photochemical isomerizations of E,E -germacra-1(10),4,7(11)-trien-8-one
Author:
Funder
Netherlands Foundation for Chemical Research
Netherlands Organization for the Advancement of Pure Research
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/recl.19780971006/fullpdf
Reference14 articles.
1. Medium-ring 1,5-dienes. Part II. The radical and electrophile-induced cyclisation of germacra-1(10),4,7(11)-triene
2. Medium-ring 1,5-dienes. Part III. Cyclisation of germacra-1(10),4,7-(11)-triene oxides
3. Medium-ring 1,5-dienes. Part IV. Reactions of germacra-1(10),4,7(11)-triene with singlet oxygen and with the triphenyl phosphite–ozone adduct
4. K. Takeda I. Horibe H. Minato J. Chem. Soc. (Chem. Comm.) 87 1971
5. Cope rearrangement of some germacrane-type furan sesquiterpenes. Part IV. Preparation of some cyclodeca-cis,trans-diene derivatives and their Cope rearrangements
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1. Germacrone: Occurrence, Synthesis, Chemical Transformations and Biological Properties;Natural Product Communications;2008-04
2. Quantumchemical calculations on the photochemistry of germacrene and germacrol. The exclusive role of the exocyclic double bond isomerization;Tetrahedron;1988-01
3. The configuration and conformation of isogermacrone. The significance of crossed conformations in olefinic cyclisations;Tetrahedron;1985-01
4. Olefin inversion;Tetrahedron;1980-01
5. Conformational dependence in the photochemistry of (E,E )-germacra-1(10),4,7(11)-triene;Recueil des Travaux Chimiques des Pays-Bas;1980
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