The EIMS fragmentation mechanisms of the sesquiterpenes corvol ethers A and B, epi-cubebol and isodauc-8-en-11-ol

Scholarly Works

• Haslina Abd Latib, E.; Moyeenul Huq, A.; Zareen, S.; Nizam Tajuddin, S. Gas chromatography mass spectrometry couple with quadrupole time-of-flight (GC-QTOF MS) as a powerful tool for profiling of oxygenated sesquiterpenes in agarwood oil. Arabian Journal of Chemistry 2023, 16, 105025. doi:10.1016/j.arabjc.2023.105025
• Tarasova, E. V.; Luchnikova, N. A.; Grishko, V. V.; Ivshina, I. B. Actinomycetes as Producers of Biologically Active Terpenoids: Current Trends and Patents. Pharmaceuticals (Basel, Switzerland) 2023, 16, 872. doi:10.3390/ph16060872
• Li, H.; Dickschat, J. S. Isotopic labelling experiments and enzymatic preparation of iso-casbenes with casbene synthase from Ricinus communis. Organic Chemistry Frontiers 2022, 9, 795–801. doi:10.1039/d1qo01707a
• Hou, A.; Dickschat, J. S. The EI-MS Fragmentation Mechanisms of the Bacterial Diterpenes Polytrichastrene A and Wanju-2,5-diene. European Journal of Organic Chemistry 2021, 2021, 6417–6423. doi:10.1002/ejoc.202101151
• Li, G.; Guo, Y.-W.; Dickschat, J. S. The mass spectrometric fragmentation mechanisms of catenulane and isocatenulane diterpenes. Organic & biomolecular chemistry 2021, 19, 2224–2232. doi:10.1039/d1ob00160d
• Hou, A.; Dickschat, J. S. On the mass spectrometric fragmentations of the bacterial sesterterpenes sestermobaraenes A-C. Beilstein journal of organic chemistry 2020, 16, 2807–2819. doi:10.3762/bjoc.16.231
• Xu, H.; Dickschat, J. S. Revision of the Cyclisation Mechanism for the Diterpene Spiroviolene and Investigations of Its Mass Spectrometric Fragmentation. Chembiochem : a European journal of chemical biology 2020, 22, 850–854. doi:10.1002/cbic.202000682
• Pereira, R. C.; Nocchi, N.; Souto, M. L.; Fernández, J. J.; Norte, M.; Duarte, H. M.; Soares, A. R. The sea-hare Aplysia brasiliana promotes induction in chemical defense in the seaweed Laurencia dendroidea and in their congeneric neighbors. Plant physiology and biochemistry : PPB 2020, 154, 295–303. doi:10.1016/j.plaphy.2020.05.020
• Said, M. S.; Navale, G. R.; Gajbhiye, J. M.; Shinde, S. S. Retracted Article: Synthesis of deuterated isopentyl pyrophosphates for chemo-enzymatic labelling methods: GC-EI-MS based 1,2-hydride shift in epicedrol biosynthesis. RSC advances 2019, 9, 28258–28261. doi:10.1039/c9ra00163h
• Said, M. S.; Navale, G. R.; Gajbhiye, J. M.; Shinde, S. S. Retracted Article: Synthesis of deuterated isopentyl pyrophosphates for chemo-enzymatic labelling methods: GC-EI-MS based 1,2-hydride shift in epicedrol biosynthesis. RSC Advances 2019, 10, 28258–28261.
• Pale-Ezquivel, I.; Aguirre-Jaimes, A.; Hernández, J.; Coates, R.; Domínguez, Z. Floral Scents in Pachira aquatica (Malvaceae): A Species with Diverse Floral Visitors in a Mexican Lowland Forests. Natural Product Communications 2018, 13. doi:10.1177/1934578x1801301034
• Rinkel, J.; Rabe, P.; Dickschat, J. S. The EI‐MS Fragmentation Mechanisms of Bacterial Sesquiterpenes and Diterpenes. European Journal of Organic Chemistry 2018, 2019, 351–359. doi:10.1002/ejoc.201800217
• Liang, J.; Liu, J.; Brown, R.; Jia, M.; Zhou, K.; Peters, R. J.; Wang, Q. Direct production of dihydroxylated sesquiterpenoids by a maize terpene synthase. The Plant journal : for cell and molecular biology 2018, 94, 847–856. doi:10.1111/tpj.13901
• Dickschat, J. S. Modern Aspects of Isotopic Labellings in Terpene Biosynthesis. European Journal of Organic Chemistry 2017, 2017, 4872–4882. doi:10.1002/ejoc.201700482
• Shinde, S. S.; Minami, A.; Chen, Z.; Tokiwano, T.; Toyomasu, T.; Kato, N.; Sassa, T.; Oikawa, H. Cyclization mechanism of phomopsene synthase: mass spectrometry based analysis of various site-specifically labeled terpenes. The Journal of antibiotics 2017, 70, 632–638. doi:10.1038/ja.2017.27
• Rabe, P.; Rinkel, J.; Nubbemeyer, B.; Köllner, T. G.; Chen, F.; Dickschat, J. S. Terpencyclasen aus sozialen Amöben. Angewandte Chemie 2016, 128, 15646–15649. doi:10.1002/ange.201608971
• Rabe, P.; Rinkel, J.; Nubbemeyer, B.; Köllner, T. G.; Chen, F.; Dickschat, J. S. Terpene Cyclases from Social Amoebae. Angewandte Chemie (International ed. in English) 2016, 55, 15420–15423. doi:10.1002/anie.201608971
• Duhamel, N.; Martin, D.; Larcher, R.; Fedrizzi, B.; Barker, D. Convenient synthesis of deuterium labelled sesquiterpenes. Tetrahedron Letters 2016, 57, 4496–4499. doi:10.1016/j.tetlet.2016.08.079

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