Organomercury hydroperoxides from cyclopropanes
β Scribed by V.I. Sokolov; O.A. Reutov
- Book ID
- 112434254
- Publisher
- Springer
- Year
- 1969
- Tongue
- English
- Weight
- 47 KB
- Volume
- 18
- Category
- Article
- ISSN
- 1573-9171
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π SIMILAR VOLUMES
Metal carbenoida are more appropriate reagent6 for the convereion of alkenee to cyclopropanee then the unselective free Cl%2 with ita tendency for CHineertion (1). Halomethyllithiur has not been ueed exteneively for thie purpose. Thie reagent, generated from dibromomethane and methyllithium in ether
## Abstract Singlet oxygen was detected from the reaction of lophine hydroperoxides 2 in the presence of 1,3βdiphenylβisobenzofuran as a singlet oxygen detector. In order to examine the substituent effect on the formation of ^1^O~2~, 2β(__p__βsubstituted phenyl) lophine peroxides 2aβc were tested.