Seto et al., 1996 - Google Patents
Preparation of (±)-2-(2, 3-2H2) jasmonic acid and its methyl ester, methyl (±)-2-(2, 3-2H2) jasmonateSeto et al., 1996
View PDF- Document ID
- 5111805016699892490
- Author
- Seto H
- Fujioka S
- Fujisawa H
- Goto K
- Nojiri H
- Yamane H
- Yoshida S
- Publication year
- Publication venue
- Bioscience, biotechnology, and biochemistry
External Links
Snippet
For use as the internal standards in a quantitative analysis of natural jasmonic acid (JA) and methyl jasmonate (JAMe) by gas chromatography-mass spectrometry-selected ion monitoring,(±)-2-(2, 3–2H2) JA and its methyl ester,(±)-2-(2, 3–2H2) JAMe, were efficiently …
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 CC\C=C/C[C@@H]1[C@@H](CC(O)=O)CCC1=O 0 title abstract description 72
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- C07C2101/12—Systems containing only non-condensed rings with a six-membered ring
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- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulfur
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulfur with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
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