Expeditious Semisynthesis of Docetaxel Using 2-Trichloromethyl-1,3-Oxazolidine as Side-Chain Protection

DOI: 10.1016/S0040-4039(00)76828-6

Source and publish data:

Tetrahedron Letters p. 3063 - 3064 (1994)

Update date:2022-08-03

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Authors:

Didier, Eric

Fouque, Elie

Commercon, Alain

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Article abstract of DOI:10.1016/S0040-4039(00)76828-6

Chloral reacts with phenylisoserine and N-Boc-phenylisoserine methyl esters to give N-unprotected 2-trichloromethyl-1,3-oxazolidines 4+4'.The corresponding oxazolidinecarboxylic acids 5+5' were esterified by 10-desacetyl-7,10-diTroc-baccatin III.Concomita

Full text of DOI:10.1016/S0040-4039(00)76828-6

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Article Doi

Expeditious Semisynthesis of Docetaxel Using 2-Trichloromethyl-1,3-Oxazolidine as Side-Chain Protection

DOI: 10.1016/S0040-4039(00)76828-6

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)76828-6

Full text of DOI:10.1016/S0040-4039(00)76828-6

Products guided by the article

R&D Labs maybe for 202741-88-6

Relevant to this article

Preparation, Ligand Substitution, and Structural Stability of (eta;3-Allyl)dicarbonylnitrosyliron Complexes

Neomycin-capped aromatic platforms: Quadruplex DNA recognition and telomerase inhibition

Diels-Alder cycloaddition of electrophilic 2H-azirines with 3-(3-(tert-butyldimethylsilyloxy)buta-1,3-dienyl)oxazolidin-2-ones. Treatment of the cycloadducts under acidic conditions

Optimization of a potent class of arylamide colony-stimulating factor-1 receptor inhibitors leading to anti-inflammatory clinical candidate 4-cyano-N -[2-(1-cyclohexen-1-yl)-4-[1-[(dimethylamino)acetyl]-4-piperidinyl]phenyl]-1 H -imidazole-2-carboxamide (JNJ-28312141)

SYNTHESIS OF CELLOBIOSE, CELLOTRIOSE, CELLOTETRAOSE, AND LACTOSE

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