The unusual stability of phenylsulfinyl carbene, signalled by (1) the ease by which it is formed unimolecularly from phenyl diazomethyl sulfoxide, (2) the lack of C-H insertion reactions, and (3) the high degree of stereoselectivity in cycloaddition to Z-2-butene and cyclohexene, 2 strongly suggests
β¦ LIBER β¦
Steric and electronic factors in the reductive cleavage of methyl-substituted phenylcyclopropanes and spiro[2.4]hepta-4,6-dienes
β Scribed by Staley, Stuart W.; Rocchio, Joseph J.
- Book ID
- 126976027
- Publisher
- American Chemical Society
- Year
- 1969
- Tongue
- English
- Weight
- 295 KB
- Volume
- 91
- Category
- Article
- ISSN
- 0002-7863
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Steric and electronic factors in the add
β
Clifford G. Venier; Mark A. Ward
π
Article
π
1978
π
Elsevier Science
π
French
β 243 KB
Electronic absorption and circular dichr
β
Browne, Alan R.; Kearney, Francis R.; Mason, Stephen F.; Paquette, Leo A.; Drake
π
Article
π
1983
π
American Chemical Society
π
English
β 945 KB
Effect of increasing electron demand upo
β
Garratt, Dennis G.; Beaulieu, Pierre L.
π
Article
π
1979
π
American Chemical Society
π
English
β 658 KB
Steric factors in the cyclization of 4-a
β
G. T. Katvalyan; Γ. A. Mistryukov
π
Article
π
1985
π
Springer
π
English
β 448 KB
Steric and electronic effects on the mec
β
Isanbor, Chukwuemeka; Emokpae, Thomas A.; Crampton, Michael R.
π
Article
π
2002
π
Royal Society of Chemistry
π
English
β 157 KB
Structures and Properties of Tris(donor)
β
Jens Wolff, J. ;Gredel, Frank ;Hillenbrand, Daniela ;Irngartinger, Hermann
π
Article
π
2006
π
John Wiley and Sons
π
English
β 832 KB
## Abstract The conformational properties of triaminoβsubstituted 1,3,5βtrinitrobenzenes were studied by Xβray crystallography, dynamic NMR spectroscopy, and semiempirical calculations. As amino substituents all possible combinations of a dialkylβ, a monoalkylamino, and an amino group were used. Al