Effect of reaction conditions and kinetics of the isomerization of β-pinene epoxide to myrtanal in the presence of Fe/MCM-41 and Fe/SBA-15
Author:
Funder
Universidad de Antioquia
Minciencias
Publisher
Springer Science and Business Media LLC
Subject
Physical and Theoretical Chemistry,Catalysis
Link
https://link.springer.com/content/pdf/10.1007/s11144-022-02220-y.pdf
Reference30 articles.
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2. Deshpande N, Parulkar A, Joshi R, Diep B, Brunelli NA (2019) Regioselective epoxide ring opening with alcohols using heterogeneous Lewis acid catalysts. J Catal 370:46–54. https://doi.org/10.1016/j.jcat.2018.11.038
3. De La Torre O, Renz M, Corma A (2010) Biomass to chemicals: rearrangement of β-pinene epoxide into myrtanal with well-defined single-site substituted molecular sieves as reusable solid Lewis-acid catalysts. Appl Catal A 380(1–2):165–171. https://doi.org/10.1016/j.apcata.2010.03.056
4. Mäki-arvela P et al (2013) Isomerization of β-pinene oxide over Sn-modified zeolites. J Mol Catal A Chem 366:228–237. https://doi.org/10.1016/j.molcata.2012.09.028
5. Breitmaier E (1997) Common fragrance and flavor materials. Wiley, Hoboken
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