Hayashi et al., 2003 - Google Patents
A Diastereocontrolled Route to (R)-(-)-Baclofen Using a Cyclopentanoid Chiral Building BlockHayashi et al., 2003
View PDF- Document ID
- 13907880851694340628
- Author
- Hayashi M
- Ogasawara K
- Publication year
- Publication venue
- Heterocycles-Sendai Institute of Heterocyclic Chemistry
External Links
Snippet
A DIASTEREOCONTROLLED ROUTE TO (R)-(–)-BACLOFEN USING A
CYCLOPENTANOID CHIRAL BUILDING BLOCK Masato Hayashi and Kunio Ogasawar
Page 1 HETEROCYCLES, Vol. 59, No. 2, 2003, pp. 785 - 791, Received, 10th October …
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 OC(=O)C[C@@H](CN)C1=CC=C(Cl)C=C1 0 title abstract description 7
Classifications
-
- 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
- C07C2101/16—The ring being unsaturated
-
- 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
- C07C2101/14—The ring being saturated
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- C07D205/02—Heterocyclic compounds containing four-membered rings with one nitrogen atom as the only ring hetero atom not condensed with other rings
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