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First total synthesis of taxol. 2. Completion of the C and D rings
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inferred← citeshttps://doi.org/10.1016/0040-4039(95)00271-dopenalex-snapshot
A convergent carbohydrate approach to the synthesis of taxol. Part 1. Ring A subunit
inferred← citeshttps://doi.org/10.1016/0040-4039(95)00272-eopenalex-snapshot
A convergent carbohydrate approach to the synthesis of taxol. Part 2. Ring C subunit
inferred← citeshttps://doi.org/10.1016/0040-4039(95)00523-fopenalex-snapshot
Enzymatic resolution of a key stereochemical intermediate for the synthesis of (−)-taxol
inferred← citeshttps://doi.org/10.1016/0040-4039(95)00897-lopenalex-snapshot
Toward the Synthesis of Taxol and its Analogs: Incorporation of Non-Aromatic C-Rings in the Pinene Pathway
inferred← citeshttps://doi.org/10.1016/0040-4039(95)01083-topenalex-snapshot
New Strategy for the Synthesis of the Taxane Diterpenes : Formation of the BC-Rings of Taxol via a [5+2]-Pyrylium Ylide-Alkene Cyclization, Ring Expansion Strategy
inferred← citeshttps://doi.org/10.1016/0040-4039(95)01172-eopenalex-snapshot
A Convergent Synthesis of Functionalized B-seco Taxane Skeletons
inferred← citeshttps://doi.org/10.1016/0040-4039(95)01244-copenalex-snapshot
Synthesis of functionalized ring a building blocks for taxoids
inferred← citeshttps://doi.org/10.1016/0040-4039(95)01836-7openalex-snapshot
PM3 conformations of C-13 Taxol® side chain methyl ester
inferred← citeshttps://doi.org/10.1016/0040-4039(95)02303-8openalex-snapshot
A versatile synthesis of (E)- and (Z)-1-halo-2-(alkoxymethyl)-1,3-butadienes and their condensation with aldehydes
inferred← citeshttps://doi.org/10.1016/0040-4039(96)00285-7openalex-snapshot
Construction of an advanced taxane synthesis intermediate with an oxygenated B-ring and a non-aromatic C-ring through intramolecular pinacol coupling at C-1C-2
inferred← citeshttps://doi.org/10.1016/0040-4039(96)00495-9openalex-snapshot
Synthesis of azetidine-type taxanes
inferred← citeshttps://doi.org/10.1016/0040-4039(96)00538-2openalex-snapshot
Diastereoselective synthesis of a taxane precursor
inferred← citeshttps://doi.org/10.1016/0040-4039(96)01383-4openalex-snapshot
Diastereoselective triple radical cyclization of a bromomethyldimethylsilyl allyl ether
inferred← citeshttps://doi.org/10.1016/0040-4039(96)01531-6openalex-snapshot
Synthesis of a highly functionalized AB taxane ring system using 1,4-dioxene
inferred← citeshttps://doi.org/10.1016/0040-4039(96)01841-2openalex-snapshot
Synthesis of a taxinine analog via the intramolecular Diels-Alder cycloaddition
inferred← citeshttps://doi.org/10.1016/0167-7799(94)90120-1openalex-snapshot
Taxol: The chemistry and structure-activity relationships of a novel anticancer agent
inferred← citeshttps://doi.org/10.1016/0378-3812(96)02991-3openalex-snapshot
Supercritical extraction and HPLC analysis of taxol from Taxus brevifolia using nitrous oxide and nitrous oxide + ethanol mixtures
inferred← citeshttps://doi.org/10.1016/0957-4166(94)80079-0openalex-snapshot
N-benzoyl-(2R,3S)-3-phenylisoserine methyl ester; a facile and convenient synthesis and resolution by entrainment
inferred← citeshttps://doi.org/10.1016/0960-894x(94)85035-6openalex-snapshot
Synthesis and biology of substituted 3′-phenyl taxol analogues
inferred← citeshttps://doi.org/10.1016/b0-08-044705-8/00259-4openalex-snapshot
One or More CH, CC, and/or CC Bonds Formed by Rearrangement
inferred← citeshttps://doi.org/10.1016/b0-08-044705-8/09009-9openalex-snapshot
References to Volume 1
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00612-1openalex-snapshot
6.09 Synthesis of Esters and Lactones
inferred← citeshttps://doi.org/10.1016/b978-0-08-100756-3.00003-0openalex-snapshot
Step-Economical Synthesis of Clinprost and Analogs Utilizing a Novel Decarboxylation Reaction
inferred← citeshttps://doi.org/10.1016/b978-0-323-90951-8.00006-0openalex-snapshot
Strategies for enhancing paclitaxel bioavailability for cancer treatment
inferred← citeshttps://doi.org/10.1016/b978-0-323-90951-8.00009-6openalex-snapshot
Taxol: Occurrence, chemistry, and understanding its molecular mechanisms
inferred← citeshttps://doi.org/10.1016/b978-0-323-90951-8.00012-6openalex-snapshot
Endophytes for the production of anticancer drug, paclitaxel
inferred← citeshttps://doi.org/10.1016/b978-0-443-27402-2.00007-3openalex-snapshot
Paclitaxel: a natural antitumor agent
inferred← citeshttps://doi.org/10.1016/b978-0-443-36542-3.00014-1openalex-snapshot
Chemical synthesis as design and construction of molecular architectures: a brief history
inferred← citeshttps://doi.org/10.1016/b978-008044992-0.00201-7openalex-snapshot
Azetidines, Azetines and Azetes: Monocyclic
inferred← citeshttps://doi.org/10.1016/b978-008045382-8.00058-7openalex-snapshot
Natural Products as Lead Sources for Drug Development
inferred← citeshttps://doi.org/10.1016/b978-008096518-5.00018-6openalex-snapshot
Azetidines, Azetines, and Azetes: Monocyclic
inferred← citeshttps://doi.org/10.1016/bs.pmch.2019.01.001openalex-snapshot
Natural product drug delivery: A special challenge?
inferred← citeshttps://doi.org/10.1016/j.abb.2004.04.016openalex-snapshot
Molecular cloning and characterization of a cytochrome P450 taxoid 2α-hydroxylase involved in Taxol biosynthesis
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2014.03.002openalex-snapshot
A rational approach to improving the biotechnological production of taxanes in plant cell cultures of Taxus spp.
inferred← citeshttps://doi.org/10.1016/j.bmc.2008.10.089openalex-snapshot
From nature to the laboratory and into the clinic
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