Asymmetric syntheses of the lactone core of tetrahydrolipstatin and tetrahydroesterastin and of the oriental hornet Vespa Orientalis pheromone
Gespeichert in:
Verfasser / Beitragende:
[I. Mineeva]
Ort, Verlag, Jahr:
2015
Enthalten in:
Russian Journal of Organic Chemistry, 51/6(2015-06-01), 842-848
Format:
Artikel (online)
Online Zugang:
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| 024 | 7 | 0 | |a 10.1134/S1070428015060044 |2 doi |
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| 100 | 1 | |a Mineeva |D I. |u Belarusian State University, pr. Nezavisimosti 4, 220030, Minsk, Belarus |4 aut | |
| 245 | 1 | 0 | |a Asymmetric syntheses of the lactone core of tetrahydrolipstatin and tetrahydroesterastin and of the oriental hornet Vespa Orientalis pheromone |h [Elektronische Daten] |c [I. Mineeva] |
| 520 | 3 | |a A synthetic approach to the lactone core of the anti-obesity drugs tetrahydrolipstatin and tetrahydroesterastin has been developed starting from readily accessible methyl (5S)-5-{[tert-butyl(dimethyl)silyl]-oxy}-3-oxohexadecanoate. (6S)-6-Undecyltetrahydro-2H-pyran-2-one, the oriental hornet Vespa Orientalis pheromone, has also been synthesized. A formal synthesis of (3S,4R,6S)-dihydroxy-6-undecyltetrahydro-2H-pyran-2-one (metabolite of a fungus separated from mangrove seeds) has been proposed. | |
| 540 | |a Pleiades Publishing, Ltd., 2015 | ||
| 773 | 0 | |t Russian Journal of Organic Chemistry |d Pleiades Publishing |g 51/6(2015-06-01), 842-848 |x 1070-4280 |q 51:6<842 |1 2015 |2 51 |o 11178 | |
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| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.1134/S1070428015060044 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 100 |E 1- |a Mineeva |D I. |u Belarusian State University, pr. Nezavisimosti 4, 220030, Minsk, Belarus |4 aut | ||
| 950 | |B NATIONALLICENCE |P 773 |E 0- |t Russian Journal of Organic Chemistry |d Pleiades Publishing |g 51/6(2015-06-01), 842-848 |x 1070-4280 |q 51:6<842 |1 2015 |2 51 |o 11178 | ||