Buchi et al., 1971 - Google Patents
New synthesis of cyclopentenones. Methyl jasmonate and jasmoneBuchi et al., 1971
- Document ID
- 1052602007438495875
- Author
- Buchi G
- Egger B
- Publication year
- Publication venue
- The Journal of Organic Chemistry
External Links
Snippet
New synthesis of cyclopentenones. Methyl jasmonate and jasmone Page 1 Notes J. Org. Chem,.,
Vol. No. 2021 Effect of Temperature on the Oxidation of TPC to TPP.— Four independent
oxidation reactions were carried out at temperatures of 150, 165, 175, and 189 (boiling point of …
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