New approach to the synthesis of macrocyclic core of cytotoxic lactone (+)-neopeltolide. Synthesis of C7-C14 segment basing on cyclopropanol intermediates
Gespeichert in:
Verfasser / Beitragende:
[I. Mineeva]
Ort, Verlag, Jahr:
2015
Enthalten in:
Russian Journal of Organic Chemistry, 51/8(2015-08-01), 1061-1070
Format:
Artikel (online)
Online Zugang:
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| 100 | 1 | |a Mineeva |D I. |u Belorussian State University, pr. Nezavisimosti 4, 220030, Minsk, Belarus |4 aut | |
| 245 | 1 | 0 | |a New approach to the synthesis of macrocyclic core of cytotoxic lactone (+)-neopeltolide. Synthesis of C7-C14 segment basing on cyclopropanol intermediates |h [Elektronische Daten] |c [I. Mineeva] |
| 520 | 3 | |a A new retrosynthetic procedure was developed for the synthesis of the macrocyclic core of a cytotoxic lactone (+)-neopeltolide utilizing cyclopropanol intermediates. The synthesis was suggested and carried out of the C7-C16 segment of (+)-neopeltolide to obtain (4S,6S)-6-[(2S)-2-hydroxypentyl]-4-methyltetrahydro-2H-pyran-2-one. The possibility was demonstrated of a formal synthesis based on the obtained product of the potential antitumor pharmaceutical (+)-neopeltolide. | |
| 540 | |a Pleiades Publishing, Ltd., 2015 | ||
| 773 | 0 | |t Russian Journal of Organic Chemistry |d Pleiades Publishing |g 51/8(2015-08-01), 1061-1070 |x 1070-4280 |q 51:8<1061 |1 2015 |2 51 |o 11178 | |
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| 950 | |B NATIONALLICENCE |P 856 |E 40 |u https://doi.org/10.1134/S1070428015080023 |q text/html |z Onlinezugriff via DOI | ||
| 950 | |B NATIONALLICENCE |P 100 |E 1- |a Mineeva |D I. |u Belorussian 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 51/8(2015-08-01), 1061-1070 |x 1070-4280 |q 51:8<1061 |1 2015 |2 51 |o 11178 | ||