The crystal structure of the acetone solvate of pentaphenylethane (C32H26 .
Large cyclic oligomers of furan and acetone. X-ray crystal structure of the hexamer and first synthesis of the nonamer
โ Scribed by F.H. Kohnke; G.L. La Torre; M.F. Parisi; S. Menzer; D.J. Williams
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- French
- Weight
- 248 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0040-4039
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๐ SIMILAR VOLUMES
]pyridines (THPP) upon the reaction with DMAD in acetonitrile or DMSO at rt underwent ring expansion, affording tetrahydropyrrolo[2,3-d]azocines; these latter compounds have not previously been reported in the literature. The crystal structure and conformation of these derivatives was established by
The synthesis and X-ray crystal structure determination of a novel metal-terphenyl derivative, namely DmpAuPPh 3 (1), is reported (Dmp = 2,6-dimesitylphenyl). Complex 1 is synthesized by the reaction of one equivalent of DmpLi with one equivalent of Ph 3 PAuCl in tetrahydrofuran at room temperature