Abstract
InIII triflate-catalysed addition of thiols and thiocarboxylic acids to camphene under mild conditions has allowed the functionalisation of the alkene for the first time, with suppression of the classical rearrangement of the camphene terpene skeleton to isobornane structures. © Wiley-VCH Verlag GmbH & Co. KGaA, 2007.
Original language | English |
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Pages (from-to) | 2464-2469 |
Journal | European Journal of Organic Chemistry |
Issue number | 15 |
DOIs | |
Publication status | Published - 25 Jun 2007 |
Keywords
- Camphene
- Hydrothiolation
- Indium triflate
- Rearrangement
- Thioacetylation