Burns et al., 1978 - Google Patents
A new approach to the construction of diamondoid hydrocarbons. Synthesis of anti-tetramantaneBurns et al., 1978
- Document ID
- 5600048559241853346
- Author
- Burns W
- McKervey M
- Mitchell T
- Rooney J
- Publication year
- Publication venue
- Journal of the American Chemical Society
External Links
Snippet
A new approach to the construction of diamondoidhydrocarbons is described. The method is general and could, in principle, be used as either a single or a double homologation of any lower member of the diamondiod series into a higher mem-ber. It is illustrated by the …
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 C1C(CC2C3C45)CC6C2CC52CC5CC7C2C6C13CC7C4C5 0 title abstract description 16
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- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/587—Unsaturated compounds containing a keto groups being part of a ring
- C07C49/657—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings
- C07C49/665—Unsaturated compounds containing a keto groups being part of a ring containing six-membered aromatic rings a keto group being part of a condensed ring system
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2101/00—Systems containing only non-condensed rings
- C07C2101/06—Systems containing only non-condensed rings with a five-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2101/00—Systems containing only non-condensed rings
- C07C2101/12—Systems containing only non-condensed rings with a six-membered ring
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