and references cited therein. [I 11 One route to (E)-I-lithio-I-alkenes which circumvents the (Q-I-halo-Ialkenes is the reaction of (E)-I-tri-n-butylstannyl-I-alkenes with n-butyllithium described by E.
Trapping of the 1,4-Dipole Formed in the 2 + 2-Cycloaddition of Tetracyanoethylene to Enol Ethers
β Scribed by Prof. Rolf Huisgen; Dipl.-Chem. Reinhard Schug; Dr. Gerd Steiner
- Publisher
- John Wiley and Sons
- Year
- 1974
- Tongue
- English
- Weight
- 216 KB
- Volume
- 13
- Category
- Article
- ISSN
- 0044-8249
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
The [4 2] cycloaddition of cyclopentadiene to the (2R )-bornane-10,2-sultam derivative (Γ)-1b of fumaric monomethyl ester proceeds with high endo and p-facial diastereoselectivity in the presence of 0.5 mol-equiv. of TiCl 4 . The major diastereoisomer endo-(2R,3R )-2b, isolated in 87% yield by cryst
## 3,5-diones The photoaddition of 4-methyl-1,2,4-triazoline-3,5-dione (4-MTAD) with a wide variety of acyclic, cyclic and crown aliphatic ethers has been investigated. Monochromatic (Ξ» = 514.5 nm) or polychromatic (Ξ» Υ 310 nm) irradiations give identical mono-urazolyl ethers as reaction products.