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Semisynthesis of Taxol (R): an improved procedure far the isolation of 10-deacetylbaccatin III

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1999
JSCS9-01.pdf (1.953Mb)
Аутори
Saičić, Radomir N.
Matović, Radomir
Čeković, Živorad
Чланак у часопису (Објављена верзија)
Метаподаци
Приказ свих података о документу
Апстракт
From the needles of domestic yew, (Taxus baccata), 10-deacetylbaccatin III (10-DAB) call be isolated in quantities of up to 297 mg per kg of fresh needles. Additional quantities of 10-DAB call be obtained from the extract by NaBH4 mediated reductive hydrolysis of baccatin esters. A four-step procedure converts 10-DAB into taxol in 58% overall yield.
Кључне речи:
anti-tumor agents / taxol / natural products / semisynthesis
Извор:
Journal of the Serbian Chemical Society, 1999, 64, 9, 497-503
Издавач:
  • Serbian Chemical Soc, Belgrade

DOI: 10.2298/JSC9909497S

ISSN: 0352-5139

WoS: 000082557600001

Scopus: 2-s2.0-0038929346
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2
2
URI
http://cer.ihtm.bg.ac.rs/handle/123456789/2777
Колекције
  • Radovi istraživača / Researchers' publications
Институција
IHTM
TY  - JOUR
AU  - Saičić, Radomir N.
AU  - Matović, Radomir
AU  - Čeković, Živorad
PY  - 1999
UR  - http://cer.ihtm.bg.ac.rs/handle/123456789/2777
AB  - From the needles of domestic yew, (Taxus baccata), 10-deacetylbaccatin III (10-DAB) call be isolated in quantities of up to 297 mg per kg of fresh needles. Additional quantities of 10-DAB call be obtained from the extract by NaBH4 mediated reductive hydrolysis of baccatin esters. A four-step procedure converts 10-DAB into taxol in 58% overall yield.
PB  - Serbian Chemical Soc, Belgrade
T2  - Journal of the Serbian Chemical Society
T1  - Semisynthesis of Taxol (R): an improved procedure far the isolation of 10-deacetylbaccatin III
VL  - 64
IS  - 9
SP  - 497
EP  - 503
DO  - 10.2298/JSC9909497S
ER  - 
@article{
author = "Saičić, Radomir N. and Matović, Radomir and Čeković, Živorad",
year = "1999",
url = "http://cer.ihtm.bg.ac.rs/handle/123456789/2777",
abstract = "From the needles of domestic yew, (Taxus baccata), 10-deacetylbaccatin III (10-DAB) call be isolated in quantities of up to 297 mg per kg of fresh needles. Additional quantities of 10-DAB call be obtained from the extract by NaBH4 mediated reductive hydrolysis of baccatin esters. A four-step procedure converts 10-DAB into taxol in 58% overall yield.",
publisher = "Serbian Chemical Soc, Belgrade",
journal = "Journal of the Serbian Chemical Society",
title = "Semisynthesis of Taxol (R): an improved procedure far the isolation of 10-deacetylbaccatin III",
volume = "64",
number = "9",
pages = "497-503",
doi = "10.2298/JSC9909497S"
}
Saičić RN, Matović R, Čeković Ž. Semisynthesis of Taxol (R): an improved procedure far the isolation of 10-deacetylbaccatin III. Journal of the Serbian Chemical Society. 1999;64(9):497-503
Saičić, R. N., Matović, R.,& Čeković, Ž. (1999). Semisynthesis of Taxol (R): an improved procedure far the isolation of 10-deacetylbaccatin III.
Journal of the Serbian Chemical SocietySerbian Chemical Soc, Belgrade., 64(9), 497-503.
https://doi.org/10.2298/JSC9909497S
Saičić Radomir N., Matović Radomir, Čeković Živorad, "Semisynthesis of Taxol (R): an improved procedure far the isolation of 10-deacetylbaccatin III" 64, no. 9 (1999):497-503,
https://doi.org/10.2298/JSC9909497S .

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