Synthetic terpenoids in the world of fragrances: Iso E Super® is the showcase

Alexey Stepanyuk and Andreas Kirschning
Beilstein J. Org. Chem. 2019, 15, 2590–2602. https://doi.org/10.3762/bjoc.15.252

Cite the Following Article

Synthetic terpenoids in the world of fragrances: Iso E Super® is the showcase
Alexey Stepanyuk and Andreas Kirschning
Beilstein J. Org. Chem. 2019, 15, 2590–2602. https://doi.org/10.3762/bjoc.15.252

How to Cite

Stepanyuk, A.; Kirschning, A. Beilstein J. Org. Chem. 2019, 15, 2590–2602. doi:10.3762/bjoc.15.252

Download Citation

Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window below.
Citation data in RIS format can be imported by all major citation management software, including EndNote, ProCite, RefWorks, and Zotero.

Presentation Graphic

Picture with graphical abstract, title and authors for social media postings and presentations.
Format: PNG Size: 214.1 KB Download

Citations to This Article

Up to 20 of the most recent references are displayed here.

Scholarly Works

  • González-Minero, F. J.; Bravo-Díaz, L.; Moreno-Toral, E. Pharmacy and Fragrances: Traditional and Current Use of Plants and Their Extracts. Cosmetics 2023, 10, 157. doi:10.3390/cosmetics10060157
  • Qu, Y.; Xie, D.; Liu, Y. Emissions of Volatile Organic Compounds from Human Occupants in a Student Office: Dependence on Ozone Concentration. ACS environmental Au 2023, 4, 3–11. doi:10.1021/acsenvironau.3c00043
  • Jezierski, T.; Dzięcioł, M. Canine Detection of Cancer in Humans: Expectations Versus Reality. Chemical Signals in Vertebrates 15; Springer International Publishing, 2023; pp 453–487. doi:10.1007/978-3-031-35159-4_22
  • Aberle, B.; Kowalczyk, D.; Massini, S.; Egler-Kemmerer, A.-N.; Gergel, S.; Hammer, S. C.; Hauer, B. Methylation of Unactivated Alkenes with Engineered Methyltransferases To Generate Non-natural Terpenoids. Angewandte Chemie (International ed. in English) 2023, 62, e202301601. doi:10.1002/anie.202301601
  • Aberle, B.; Kowalczyk, D.; Massini, S.; Egler‐Kemmerer, A.; Gergel, S.; Hammer, S. C.; Hauer, B. Methylierung nicht‐aktivierter Alkene mit modifizierten Methyltransferasen zur Diversifizierung von Terpenoiden. Angewandte Chemie 2023, 135. doi:10.1002/ange.202301601
  • Rocha, F.; Ratola, N.; Homem, V. Fragrances in the Environment: Properties, Applications, and Emissions. The Handbook of Environmental Chemistry; Springer Berlin Heidelberg, 2023. doi:10.1007/698_2023_983
  • Rádis-Baptista, G. Do Synthetic Fragrances in Personal Care and Household Products Impact Indoor Air Quality and Pose Health Risks?. Journal of xenobiotics 2023, 13, 121–131. doi:10.3390/jox13010010
  • Zhou, Y.; Luo, P.; Xu, L.-J.; Xu, W.; Jiang, R.-W. A new fan-like adaptive porous organic cage for the structure determination of liquid perfume molecules. Organic Chemistry Frontiers 2023, 10, 1119–1127. doi:10.1039/d2qo02006h
  • Costa, J. A. V.; Cassuriaga, A. P. A.; Moraes, L.; Morais, M. G. Biosynthesis and potential applications of terpenes produced from microalgae. Bioresource Technology Reports 2022, 19, 101166. doi:10.1016/j.biteb.2022.101166
  • Kleoff, M.; Kiler, P.; Heretsch, P. Synthesis of odorants in flow and their applications in perfumery. Beilstein journal of organic chemistry 2022, 18, 754–768. doi:10.3762/bjoc.18.76
  • Kuhwald, C.; Türkhan, S.; Kirschning, A. Inductive heating and flow chemistry - a perfect synergy of emerging enabling technologies. Beilstein journal of organic chemistry 2022, 18, 688–706. doi:10.3762/bjoc.18.70
  • Sommer, S.; Lang, L. M.; Drummond, L.; Buchhaupt, M.; Fraatz, M. A.; Zorn, H. Odor Characteristics of Novel Non-Canonical Terpenes. Molecules (Basel, Switzerland) 2022, 27, 3827. doi:10.3390/molecules27123827
  • Lin, Z.; Huang, B.; Ouyang, L.; Zheng, L. Synthesis of Cyclic Fragrances via Transformations of Alkenes, Alkynes and Enynes: Strategies and Recent Progress. Molecules (Basel, Switzerland) 2022, 27, 3576. doi:10.3390/molecules27113576
  • Vilas-Boas, S. M.; da Costa, M. C.; Coutinho, J. A. P.; Ferreira, O.; Pinho, S. P. Octanol–Water Partition Coefficients and Aqueous Solubility Data of Monoterpenoids: Experimental, Modeling, and Environmental Distribution. Industrial & Engineering Chemistry Research 2022, 61, 3154–3167. doi:10.1021/acs.iecr.1c04196
  • Riad, N.; Zahi, M. R.; Bouzidi, N.; Daghbouche, Y.; Touafek, O.; El Hattab, M. Occurrence of Marine Ingredients in Fragrance: Update on the State of Knowledge. Chemistry 2021, 3, 1437–1463. doi:10.3390/chemistry3040103
  • Valencia, A.; Romero-Orejon, F. L.; Viñas-Ospino, A.; Barriga-Rodriguez, D.; Muñoz, A. M.; Ramos-Escudero, F. Sacha Inchi Seed ( Plukenetia volubilis L.) Oil: Terpenoids. Terpenes and Terpenoids - Recent Advances; IntechOpen, 2021. doi:10.5772/intechopen.96690
  • Heeley-Hill, A. C.; Grange, S. K.; Ward, M. W.; Lewis, A. C.; Owen, N.; Jordan, C.; Hodgson, G.; Adamson, G. Frequency of use of household products containing VOCs and indoor atmospheric concentrations in homes. Environmental science. Processes & impacts 2021, 23, 699–713. doi:10.1039/d0em00504e
  • Xiaoda, W.; Hong, P.; Kiss, A. A.; Wang, Q.; Li, L.; Wang, H.; Qiu, T. From Batch to Continuous Sustainable Production of 3-Methyl-3-penten-2-one for Synthetic Ketone Fragrances. ACS Sustainable Chemistry & Engineering 2020, 8, 17201–17214. doi:10.1021/acssuschemeng.0c05908
  • Rüthi, F.; Schröder, F. Total Synthesis of (−)-Rotundone and (−)-epi-Rotundone from Monoterpene Precursors. Helvetica Chimica Acta 2020, 103. doi:10.1002/hlca.202000129
  • Li, L.; Hong, P.; Kiss, A. A.; Tian, H.; Xiaoda, W.; Qiu, T. Unraveling the reaction route and kinetics of 3‐methyl‐3‐penten‐2‐one synthesis for synthetic ketone fragrances. Journal of Chemical Technology & Biotechnology 2020, 96, 48–63. doi:10.1002/jctb.6543
Other Beilstein-Institut Open Science Activities