Abstract
Cyclopentenyl carbinols are oxidatively cleaved and cyclized into a class of terpenylic acid analogues in the presence of oxone and sodium periodate in good yields. Graphical abstract: [Figure not available: see fulltext.]
Original language | English |
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Pages (from-to) | 1885-1889 |
Number of pages | 5 |
Journal | Chemical Papers |
Volume | 76 |
Issue number | 3 |
DOIs | |
State | Published - Mar 2022 |
Keywords
- Cyclopentenyl carbinol
- Lactonization
- Oxidative cleavage
- Oxone
- Terpenylic acid