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The conformation of cis,cis -cyclodeca-3,8-diene-1,6-dione

โœ Scribed by Carrell, Horace L.; Roberts, Bryan W.; Donohue, Jerry.; Vollmer, John J.


Book ID
127192206
Publisher
American Chemical Society
Year
1968
Tongue
English
Weight
263 KB
Volume
90
Category
Article
ISSN
0002-7863

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Solution photochemistry. I. The photolys
โœ John R. Scheffer; Mel L. Lungle ๐Ÿ“‚ Article ๐Ÿ“… 1969 ๐Ÿ› Elsevier Science ๐ŸŒ French โš– 195 KB

A study of the photochemistry of cis cis-cyclodeca-3,8-diem-1,6-dione (I) has recently -Ireported (1). We have been independently engaged in studying the photochemistry of I and present our results which differ significantly from those previously reported (1).

Photolytic transformations of cis, cis-c
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The recent communication by Shani (1) in which the photolysis of cis, cis-cyclodeca---3,8-diene-1, 6-dione (I) is reported to give cis,\*, cis-tricyclo[5. 3. 0. 0 2, (+d ecane-4,9--dione prompts us to report results we had obtained independently which lead to the cis, -anti, cis (IIa) stereochemical

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The photoohemical reaction of g&,EQS";yoloocta-lr5-diene (I) yielded the cross-bonded tricycle [3.3.0.02'6] octane (II) (1) and that of the cyclohexa-1,4-diene III led to the rearranged bicyclic product IV (2). We wish to report the p$toohemical reaction of the &&&-cyclodeca-1,6-diene system (3), (

The conformation of cyclodeca-1,6-diene
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Intramolecular photocyclization of cis,
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The transannular photocyclization of the cis,cis-cyclodecs-1,6+lienes to the tricyolo 5.3.0.02p6 --C 3 decane (1) may be explained due to the proximity in space of the two double bonds in the ~~hamnocks conformation I (2). Hence, in an intramolecular photocyclization of the isomeric trans,trans,cycl