## Abstract The chemistry of the highly substituted cyclobutanone derivative 2, which is easily accessible from 1, is dominated by the steric hindrance caused by the substitutents: Reduction with hydride reagents and nucleophilic additions with methyllithium are less stereoselective than correspond
β¦ LIBER β¦
Stereochemistry of the thermal isomerization of bicyclo[3.2.0]hept-2-ene to bicyclo[2.2.1]hept-2-ene
β Scribed by Baldwin, John E.; Belfield, Kevin D.
- Book ID
- 121422176
- Publisher
- American Chemical Society
- Year
- 1988
- Tongue
- English
- Weight
- 886 KB
- Volume
- 110
- Category
- Article
- ISSN
- 0002-7863
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Rearrangement of a Bicyclo[3.2.0]hept-2-
β
Behrendt, Uwe ;Gabor, Barbara ;Mynott, Richard ;ButenschΓΆn, Holger
π
Article
π
2006
π
John Wiley and Sons
π
English
β 996 KB
Thermal Isomerization of Bicyclo[3.2.0]h
β
Cargill, Robert L.; Pond, David M.
π
Article
π
1966
π
American Chemical Society
π
English
β 267 KB
ChemInform Abstract: Rearrangement of a
β
U. BEHRENDT; B. GABOR; R. MYNOTT; H. BUTENSCHOEN
π
Article
π
2010
π
John Wiley and Sons
β 30 KB
Radical anions of bicyclo[2.2.1]hept-5-e
β
Blankespoor, Ronald L.
π
Article
π
1974
π
American Chemical Society
π
English
β 326 KB
Isomerization of 5-(cyclopentadienyliden
β
D. V. Petrov
π
Article
π
1999
π
Springer
π
English
β 146 KB
The thermal isomerization of 6-difluorom
β
William R. Dolbier Jr.; Carlos A. Piedrahita; Basil H. Al-Sader
π
Article
π
1979
π
Elsevier Science
π
French
β 192 KB
The thermal isomerization of 6-difluoromethylenebicyclo[3.2.0]hept-2-ene proceec via two competing 1,3-sigmatropic processes, with an E, nearly identical to that of the hydrocarbon. Sigmatropic isomerizations of the 6-methylenebicyclo[3.2.O]hept-2-ene system have been examined extensively by Hasselm