AIBN-initiated radical reactions of 5-membered cyclic xanthates, 1,3-oxathiolane-2-thiones, with tributyltin hydride are described. Alkenes are formed at 0.025 M concentration of tributyltin hydride, whereas a higher concentration (0.25 M ) gives 1,3-oxathiolanes. A mixture of alkene and 1,3-0xathio
โฆ LIBER โฆ
ChemInform Abstract: Radical Reduction of Cyclic Xanthates: Formation of Alkenes and/or 1,3- Oxathiolanes from 1,3-Oxathiolane-2-thiones.
โ Scribed by J. UENISHI; T. KUNUGI; Y. KUBO
- Book ID
- 112025021
- Publisher
- John Wiley and Sons
- Year
- 2010
- Weight
- 31 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0931-7597
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Radical reduction of cyclic xanthates: F
โ
Jun'ichi Uenishi; Takayuki Kunugi; Yuki Kubo
๐
Article
๐
1995
๐
John Wiley and Sons
๐
English
โ 734 KB
ChemInform Abstract: Reaction of 1,3-Thi
โ
Milen Blagoev; Anthony Linden; Heinz Heimgartner
๐
Article
๐
2010
๐
John Wiley and Sons
โ 33 KB
๐ 1 views
ChemInform Abstract: A Bimetallic Alumin
โ
William Clegg; Ross W. Harrington; Michael North; Pedro Villuendas
๐
Article
๐
2010
๐
John Wiley and Sons
โ 51 KB
๐ 1 views
ChemInform Abstract: Synthesis of 1,3-Ox
โ
SHAMSUZZAMAN SHAMSUZZAMAN; A. SALIM
๐
Article
๐
2010
๐
John Wiley and Sons
โ 26 KB
๐ 2 views
ChemInform Abstract: Photochemically Ini
โ
M. LESAGE; P. ARYA
๐
Article
๐
2010
๐
John Wiley and Sons
โ 34 KB
Reaction of Optically Active Oxiranes wi
โ
Changchun Fu; Anthony Linden; Heinz Heimgartner
๐
Article
๐
2011
๐
John Wiley and Sons
๐
German
โ 247 KB
๐ 1 views
## Abstract The SnCl~4~โcatalyzed reaction of (โ)โthiofenchone (=1,3,3โtrimethylbicyclo[2.2.1]heptaneโ2โthione; **10**) with (__R__)โ2โphenyloxirane ((__R__)โ**11**) in anhydrous CH~2~Cl~2~ at โ60ยฐ led to two spirocyclic, stereoisomeric 4โphenylโ1,3โoxathiolanes **12** and **13** __via__ a regiosel