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Cite the Following Article
The stereochemical course of 2-methylisoborneol biosynthesis
Binbin Gu, Anwei Hou and Jeroen S. Dickschat
Beilstein J. Org. Chem. 2022, 18, 818–824.
https://doi.org/10.3762/bjoc.18.82
How to Cite
Gu, B.; Hou, A.; Dickschat, J. S. Beilstein J. Org. Chem. 2022, 18, 818–824. doi:10.3762/bjoc.18.82
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- Andreas, M. P.; Giessen, T. W. The biosynthesis of the odorant 2-methylisoborneol is compartmentalized inside a protein shell. Nature communications 2024, 15, 9715. doi:10.1038/s41467-024-54175-4
- Dickschat, J. S.; Quan, Z.; Schnakenburg, G. A Case of Convergent Evolution: The Bacterial Sesquiterpene Synthase for 1-epi-Cubenol from Nonomuraea coxensis. Chembiochem : a European journal of chemical biology 2023, 24, e202300581. doi:10.1002/cbic.202300581
- Gu, B.; Liang, L.-F.; Dickschat, J. S. Functions of enzyme domains in 2-methylisoborneol biosynthesis and enzymatic synthesis of non-natural analogs. Beilstein journal of organic chemistry 2023, 19, 1452–1459. doi:10.3762/bjoc.19.104
- Gu, B.; Dickschat, J. S. Functional Characterisation of Highly Conserved and Structurally Prominent Residues of 2-Methylisoborneol Synthase. Chemistry (Weinheim an der Bergstrasse, Germany) 2023, 29, e202300775. doi:10.1002/chem.202300775