Highly Unsaturated Cyclobutane Derivatives
✍ Scribed by Richard P. Johnson
- Publisher
- John Wiley and Sons
- Year
- 2007
- Weight
- 11 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0931-7597
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📜 SIMILAR VOLUMES
a-Halogenated amines are formed by cleavage of aminals with acid halides. Analogously, N,N,N',N'-tetraalkylmethylenediamines react with sulfonic anhydrides t o yield dialkylmethyleneimonium sulfonates and dialkylsulfonamides. Tetraethyl pyrophosphate reacts with aminals or a-dialkylamino ethers to p
## Abstract The first tetrathio‐substituted cyclobutane‐1,2,3,4‐tetracarbonitrile 9 was obtained by an intramolecular photoinduced [2 + 2] cycloaddition reaction of the 14‐membered macrocyclic tetrathioether 7 containing two 1,2‐dicyano‐1,2‐dithioethene units in dichloromethane in 73% yield.