Yue et al., 1996 - Google Patents
A Suzuki coupling approach to double bonds locked analogues of strobilurin AYue et al., 1996
- Document ID
- 6859449773009741010
- Author
- Yue X
- Qing F
- Sun H
- Fan J
- Publication year
- Publication venue
- Tetrahedron letters
External Links
Snippet
A Suzuki Coupling Approach to Double Bonds Locked Analogues of Strobilurin A Page 1
Pergamon Tetrahedron Letters, Vol. 37, No, 45, pp. 8213-8216, 1996 Copyright © 1996
Elsevier Science Ltd Primed in Great Britain. All rights reserved PII: S0040-4039(96)01870-9 …
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 CO\C=C(\C(=O)OC)/C(/C)=C\C=C\C1=CC=CC=C1 0 title abstract description 8
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- C—CHEMISTRY; METALLURGY
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- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C317/00—Sulfones; Sulfoxides
- C07C317/24—Sulfones; Sulfoxides having sulfone or sulfoxide groups and doubly-bound oxygen atoms bound to the same carbon skeleton
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