The London medical and physical journal
Tegart E.
PMID: 30494789
Lond Med Phys J. 1825 Aug;54(318):105-110.
No abstract available.
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Tegart E. Remarks on the Medicinal Properties of the Croton Oil. Lond Med Phys J. 1825;54(318):105-110
Tegart, E. (1825). Remarks on the Medicinal Properties of the Croton Oil. The London medical and physical journal, 54(318), 105-110.
Tegart, Ed. "Remarks on the Medicinal Properties of the Croton Oil." The London medical and physical journal vol. 54,318 (1825): 105-110.
Tegart E. Remarks on the Medicinal Properties of the Croton Oil. Lond Med Phys J. 1825 Aug;54(318):105-110. PMID: 30494789; PMCID: PMC5641011.
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Chemistry, an Asian journal
Egart B, Czekelius C.
PMID: 24956967
Chem Asian J. 2014 Aug;9(8):2088-91. doi: 10.1002/asia.201402234. Epub 2014 Jun 24.
The intramolecular bromoamination of allylated aldoxime ethers leads first to isoxazolidinium salts which then undergo a skeletal rearrangement to form bromo-5,6-dihydro-4H-1,3-oxazines. Aliphatic aldoxime ethers with α-protons undergo multiple brominations before rearrangement.
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Egart B, Czekelius C. Stereoselective bromocyclization of allylated aldoxime ethers. Chem Asian J. 2014;9(8):2088-91doi: 10.1002/asia.201402234.
Egart, B., & Czekelius, C. (2014). Stereoselective bromocyclization of allylated aldoxime ethers. Chemistry, an Asian journal, 9(8), 2088-91. https://doi.org/10.1002/asia.201402234
Egart, Boris, and Czekelius, Constantin. "Stereoselective bromocyclization of allylated aldoxime ethers." Chemistry, an Asian journal vol. 9,8 (2014): 2088-91. doi: https://doi.org/10.1002/asia.201402234
Egart B, Czekelius C. Stereoselective bromocyclization of allylated aldoxime ethers. Chem Asian J. 2014 Aug;9(8):2088-91. doi: 10.1002/asia.201402234. Epub 2014 Jun 24. PMID: 24956967.
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The Journal of organic chemistry
Egart B, Lentz D, Czekelius C.
PMID: 23351033
J Org Chem. 2013 Mar 15;78(6):2490-9. doi: 10.1021/jo3026725. Epub 2013 Feb 21.
The intramolecular bromoamination of O-allyl-N-tosyl-hydroxylamines results in the formation of isoxazolidines via selective 5-endo-tet cyclization. This process occurs trans-selectively in high yield and diastereoselectivity. The obtained bromo-isoxazolidines provide access to other useful building blocks, such as 2-azido-aminoalcohols, diaminoalcohols, and...
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Egart B, Lentz D, Czekelius C. Diastereoselective bromocyclization of O-allyl-N-tosyl-hydroxylamines. J Org Chem. 2013;78(6):2490-9doi: 10.1021/jo3026725.
Egart, B., Lentz, D., & Czekelius, C. (2013). Diastereoselective bromocyclization of O-allyl-N-tosyl-hydroxylamines. The Journal of organic chemistry, 78(6), 2490-9. https://doi.org/10.1021/jo3026725
Egart, Boris, et al. "Diastereoselective bromocyclization of O-allyl-N-tosyl-hydroxylamines." The Journal of organic chemistry vol. 78,6 (2013): 2490-9. doi: https://doi.org/10.1021/jo3026725
Egart B, Lentz D, Czekelius C. Diastereoselective bromocyclization of O-allyl-N-tosyl-hydroxylamines. J Org Chem. 2013 Mar 15;78(6):2490-9. doi: 10.1021/jo3026725. Epub 2013 Feb 21. PMID: 23351033.
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