Methyl 3-hydroxybutanoate |
Formula: | C5H10O3 |
CAS#: | 1487-49-6 |
MW: | 118.13 |
[MS]
[ NMR ]
[ Kovats ]
[Behavioural function]
[Occurrence in flower]
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Reference(s) for synthesis of Methyl 3-hydroxybutanoate [me-3-hydroxybutanoate]
Bette, V., Mortreux, A., Lehmann, C.W., and Carpentier, J.-F. 2003. Direct Zn-diamine promoted reduction of C=O and C=N bonds by polymethylhydrosiloxane in methanol. Chem. Comm. 3:332-333. |
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Kamitori, Y., Hojo, M., Masuda, R., Inoue, T., and Izumi, T. Selective reduction of ketoesters to hydroxyesters with the use of lithium aluminum hydride in the presence of silica gel. Tetrahedron Lett. 23:4585-4588. |
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Kurcok, P., Jedlinski, Z., and Kowalczuk, M. 1993. Reactions of ß-lactones with potassium alkoxides and their complexes with 18-crown-6 in aprotic solvents. J. Org. Chem. 58:4219-4220. |
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Ronald, R.C., and Gurusiddaiah, S. 1980. Grahamimycin A1: a novel dilactone antibiotic from cytospora. Tetrahedron Lett. 21:681-684. |
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Swaren, P., Massova, I., Bellettini, J.R., Bulychev, A., and Maveyraud, L. 1999. Elucidation of mechanism of inhibition and X-ray structure of the TEM-1 ß-lactamase from Escherichia coli inhibited by a N-sulfonyloxy-ß-lactam. J. Am. Chem. Soc. 121:5353-5359. |
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