New approach to the synthesis of macrocyclic core of cytotoxic lactone (+)-neopeltolide. Synthesis of C7-C14 segment basing on cyclopropanol intermediates

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)
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024 7 0 |a 10.1134/S1070428015080023  |2 doi 
035 |a (NATIONALLICENCE)springer-10.1134/S1070428015080023 
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 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