Results 11 to 20 of about 4,048 (209)
Background: Taxol∗ is a natural product produced by the Pacific Yew, Taxus brevifolia, that has emerged as a prominent chemotherapeutic agent for the treatment of solid tumors.
Scott, Z.A. +3 more
core +3 more sources
Synthesis and Cytotoxicity of 7,9-O-Linked Macrocyclic C-Seco Taxoids
A series of novel 7,9-O-linked macrocyclic taxoids together with modification at the C2 position were synthesized, and their cytotoxicities against drug-sensitive and P-glycoprotein and βIII-tubulin overexpressed drug-resistant cancer cell lines were ...
Yu Zhao +4 more
doaj +2 more sources
Lignans, biflavones and taxoids from Himalayan Taxus baccata
Chemical investigation of the twigs (separated from the needles) of the Himalayan yew, Taxus baccata, has culminated in the isolation of a new lignan, 4'-O-demethylsuchilactone, along with eight phenolic compounds, (−)-rhododendrol, (−)-rhododendrin ...
Das, B. +3 more
core +3 more sources
Paclitaxel biological synthesis promotes the innovation of anti-cancer drugs. [PDF]
Clinical and Translational Medicine, Volume 15, Issue 2, February 2025.
Zhang X, Liu G, Yan J.
europepmc +2 more sources
Electrosynthetic C−O Bond Activation in Alcohols and Alcohol Derivatives
Deoxygenative transformations of alcohols and their derivatives are often challenging due to the thermodynamic penalty associated with the cleavage of the C−O bond. This Review includes preparative protocols and their mechanistic aspects for the activation and functionalization of C−O bonds, detailing direct and indirect electrosynthetic methods, as ...
Piret Villo +3 more
wiley +2 more sources
Background Taxol is an efficient anticancer drug accumulated in Taxus species. Pseudotaxus chienii is an important member of Taxaceae, however, the level of six taxoids in P. chienii is largely unknown. Results High accumulation of 10-DAB, taxol, and 7-E-
Chunna Yu +7 more
doaj +1 more source
Synthetic studies towards d-modified paclitaxel analogues [PDF]
A synthetic sequence has been developed for the preparation of 9,10-O-diacetyl-4-desmethylene-4β-(3-butenyl)-4α-hydroxy-5-O-mesyltaxicin I-1,2-carbonate 3, an intermediate in the attempted synthesis of cyclobutane paclitaxel analogue.
Matović Radomir +2 more
doaj +1 more source
Herein, electroreductive C−OH bond activation and subsequent deoxygenative C−H and C−C bond formation is demonstrated for non‐derivatized benzylic and propargylic alcohols. The cathodic transformations proceed via carbanions, formed via radical‐polar crossover, and are efficiently balanced by anodic oxidation of borohydride additives, a strategy that ...
Piret Villo +8 more
wiley +1 more source
Reactions of α-4(20)-epoxy-5-O-mesyltriacetyltaxicine I induced by Bf3·Et2O/Bu4NBr [PDF]
The reaction of α-4(20)-epoxy-5-O-mesyltriacetyltaxicine I (2) with BF3·Et2O/Bu4NBr can give rise to 4 different products. Each of these products can be obtained selectively, under the appropriate reaction conditions.
Ferjančić Zorana +3 more
doaj +1 more source
Synthesis and Structure‐Activity Relationship Studies of C(13)‐Desmethylene‐(−)‐Zampanolide Analogs
Reduced or demethylated variants of a C(13)‐desmethylene congener of the marine microtubule stabilizer (−)‐zampanolide have been prepared by HWE‐based macrocyclization and stereoselective construction of the hemiaminal center in the side chain. While all modifications led to reduced growth inhibitory activity, the 2,3‐dihydro and the C(17)‐desmethyl ...
Tobias M. Brütsch +10 more
wiley +1 more source

