Dynamic kinetic resolution of α-chloro β-keto esters and phosphonates: Hemisynthesis of Taxotere® through Ru-DIFLUORPHOS asymmetric hydrogenation

Tetrahedron Asymmetry

Volumn 21, Issue 11-12, 2010, Pages 1436-1446

  Prévost, Sébastien ^a   Gauthier, Sébastien ^a   De Andrade, Maria Cristina Caño ^a   Mordant, Céline ^a   Touati, Ali Rhida ^b   Lesot, Philippe ^c   Savignac, Philippe ^d   Ayad, Tahar ^a   Phansavath, Phannarath ^a   Ratovelomanana Vidal, Virginie ^a   Genêt, Jean Pierre ^a  

^a PSL RESEARCH UNIVERSITY   (France)

^b FACULTÉ DES SCIENCES DE MONASTIR   (Tunisia)

^c UNIVERSITÉ PARIS SUD   (France)

^d NONE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

3 (TERT BUTOXYCARBONYL) 2 (4 METHOXYPHENYL) 4 PHENYL 1,3 OXAZOLIDINE 5 CARBOXYLIC ACID; 3 (TERT BUTOXYCARBONYL) 2 (4 METHOXYPHENYL) 4 PHENYL 1,3 OXAZOLIDINE 5 METHANOATE; ALPHA CHLORO BETA HYDROXYESTER; ALPHA CHLORO BETA HYDROXYPHOSPHONATE; ALPHA CHLORO BETA KETO ESTER; BENZOYL ESTER; BIS O (2,2,2 TRICHLOROETHOXYCARBONYL) DOCETAXEL; DIETHYL 1 CHLORO 2 (4 CHLORO PHENYL) 2 HYDROXY ETHYLPHOSPHONATE (1R,2S); DIETHYL 1 CHLORO 2 (4 CHLORO PHENYL) 2 OXO ETHYLPHOSPHONATE; DIETHYL 1 CHLORO 2 HYDROXY 2 PHENYL ETHYL PHOSPHONATE (1R,2S); DIETHYL 1 CHLORO 2 HYDROXYBUTYLPHOSPHONATE (1R,2S); DIETHYL 1 CHLORO 2 HYDROXYPROPYLPHOSPHONATE (1R,2S); DIETHYL 1 CHLORO 2 OXOBUTYLPHOSPHONATE; DIETHYL 1 CHLORO 2 OXOPROPYLPHOSPHONATE; DIETHYL 1 CHLORO 2 PHENYL ETHYL PHOSPHONATE; DIETHYL 1 CHLORO 3 METHYL 2 HYDROXYBUTYLPHOSPHONATE (1R,2S); DIETHYL 1 CHLORO 3 METHYL 2 OXOBUTYLPHOSPHONATE; DIETHYL 1 CHLORO 3,3 DIMETHYL 2 OXOBUTYLPHOSPHONATE; DIETHYL 1 CHLOROMETHYLPHOSPHONATE; DOCETAXEL; ESTER; METHYL (2R,3R) 2 CHLORO 3 HYDROXY 3 PHENYL PROPANOATE (2R,3R); METHYL (2S,3S) 2 HYDROXY 3 (N TERT BUTOXYCARBONYLAMINO) 3 PHENYL PROPANOATE; METHYL (2S,3S) 3 AZIDO 2 HYDROXY 3 PHENYL PROPANOATE; METHYL 2 CHLORO 3 OXO 3 PHENYL PROPANOATE; METHYL 3 OXO 3 PHENYL PROPANOATE; PHOSPHONIC ACID DERIVATIVE; RUTHENIUM; TRANS METHYL (2S,3R) 3 PHENYL GLYCIDATE (2S,3R); UNCLASSIFIED DRUG; UNINDEXED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; CHEMICAL STRUCTURE; DIASTEREOISOMER; DYNAMIC KINETIC RESOLUTION; DYNAMICS; ENANTIOMER; HYDROGENATION; PRIORITY JOURNAL; SYNTHESIS;

EID: 77956649773     PISSN: 09574166     EISSN: 1362511X     Source Type: Journal    
DOI: 10.1016/j.tetasy.2010.05.017     Document Type: Article

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