Highly cytotoxic 7-deoxypaclitaxel analogues are obtained by a semisynthesis starting from taxine-the most abundant naturally occurring taxane diterpene fraction.
TY - JOUR
AU - Matović, Radomir
AU - Saičić, Radomir N.
PY - 1998
UR - http://cer.ihtm.bg.ac.rs/handle/123456789/2763
AB - Highly cytotoxic 7-deoxypaclitaxel analogues are obtained by a semisynthesis starting from taxine-the most abundant naturally occurring taxane diterpene fraction.
PB - Royal Soc Chemistry, Cambridge
T2 - Chemical Communications
T1 - An efficient semisynthesis of 7-deoxypaclitaxel from taxine
IS - 16
SP - 1745
EP - 1746
DO - 10.1039/a803990i
ER -
@article{
author = "Matović, Radomir and Saičić, Radomir N.",
year = "1998",
url = "http://cer.ihtm.bg.ac.rs/handle/123456789/2763",
abstract = "Highly cytotoxic 7-deoxypaclitaxel analogues are obtained by a semisynthesis starting from taxine-the most abundant naturally occurring taxane diterpene fraction.",
publisher = "Royal Soc Chemistry, Cambridge",
journal = "Chemical Communications",
title = "An efficient semisynthesis of 7-deoxypaclitaxel from taxine",
number = "16",
pages = "1745-1746",
doi = "10.1039/a803990i"
}
Matović R, Saičić RN. An efficient semisynthesis of 7-deoxypaclitaxel from taxine. Chemical Communications. 1998;(16):1745-1746
Matović, R.,& Saičić, R. N. (1998). An efficient semisynthesis of 7-deoxypaclitaxel from taxine.
Chemical CommunicationsRoyal Soc Chemistry, Cambridge.(16), 1745-1746.
https://doi.org/10.1039/a803990i
Matović Radomir, Saičić Radomir N., "An efficient semisynthesis of 7-deoxypaclitaxel from taxine", no. 16 (1998):1745-1746,
https://doi.org/10.1039/a803990i .
