Fluoroalkylethylenes of types 1 and 2 are unresponsive to the usual reagents for epoxidation, but recent methods have made the epoxides and related halohydrins readily available. Use of the reagent Xs/nSOs, which readily attacks the double bond of both 1 and 2, will be described in detail and compar
โฆ LIBER โฆ
Epoxides and Their Derivatives
โ Scribed by BIGGS, J.
- Book ID
- 109647734
- Publisher
- Nature Publishing Group
- Year
- 1966
- Tongue
- English
- Weight
- 144 KB
- Volume
- 209
- Category
- Article
- ISSN
- 0028-0836
- DOI
- 10.1038/209335a0
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Fluoroalkylethylenes and their epoxides
โ
C.G. Krespan
๐
Article
๐
1991
๐
Elsevier Science
๐
English
โ 31 KB
Organometallic Derivatives of Epoxides
โ
Dr. Ekkehard Bartmann
๐
Article
๐
1986
๐
John Wiley and Sons
๐
English
โ 233 KB
Stereoselective synthesis of vinylbenzot
โ
S. Florio; G. Ingrosso; L. Ronzini; E. Epifani
๐
Article
๐
1991
๐
Elsevier Science
๐
French
โ 551 KB
ฮฑ-Keto epoxides and their reactions Comm
โ
I. N. Nazarov; A. A. Arkhem
๐
Article
๐
1956
๐
Springer
๐
English
โ 526 KB
Thioimidates and Their Derivatives
โ
N. Nakajima; M. Ubukata
๐
Article
๐
2006
๐
John Wiley and Sons
โ 8 KB
Heteroadamantanes and their derivatives
โ
A. I. Kuznetsov; I. A. Vladimirova; T. M. Serova; A. S. Moskovkin
๐
Article
๐
1992
๐
Springer US
๐
English
โ 353 KB
9-ones through oximes and converted into 9-acetylamino-3,6-diaza-homoadamantanes with acetic anhydride. It was shown that oximes with one substituent in the nodal position are formed as one geometric isotner with the E-position of the hydroxyl group relative to the substituent.