The addition of dihalocarbenes to norbornene and Its derivatives produces an lntermdiate which Imdergoes a cyclopropyl-ally1 rearrangement. (2) The gem-dihalocyclopropane, Isolated in
The flash thermolysis of 3-isopropylidenetricyclo [ 3.2.1.02,4]oct-6-ene: A new rearrangement to the cyclooctatetraene system
โ Scribed by R. Bloch; F. Leyendecker; N. Toshima
- Book ID
- 104246827
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- French
- Weight
- 232 KB
- Volume
- 14
- Category
- Article
- ISSN
- 0040-4039
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โฆ Synopsis
to mesitylene was reported in 1 it. (2~). 18. Calibrated from relative yields.
๐ SIMILAR VOLUMES
In the preceding cosxnunication,l we noted that the ozonoly~is of 6,7-dimethoxy-exo--tricyclcf3.2.1.02'4]oct-6-ene (1) in methanol gave 7,7-dimethoxy-z-tricycq3.2.1.02'~act-6-one (2), in addition to the expected osonolysis product 3. We now wieh to report -our mechanistic studies related to this eno
Ptrgamon Press. Prlnttd III Great Brltarn. FLASH THERMOLYSIS OF 3,7-DIISOPROPYLIDENETETRACYCLO [3.3.1.02"+.06'8] NONANE. AN ACCESS TO THE PENTACYCLO [4.3.0.02'~,03~\*.057JN0N~NE SYSTEM