Synthesis of a highly functionalized AB taxane ring system using 1,4-dioxene

Tetrahedron Letters

Volumn 37, Issue 39, 1996, Pages 7013-7016

  Hanna, Issam ^a   Prangé, Thierry ^b   Zeghdoudi, Rachida ^a  

^a LABORATOIRE DE SYNTHÈSE ORGANIQUE   (France)

^b CNRS   (France)

Author keywords

[No Author keywords available]

Indexed keywords

TAXANE DERIVATIVE;

ARTICLE; DRUG SYNTHESIS; REACTION ANALYSIS; STEREOCHEMISTRY;

EID: 16044373966     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)01531-6     Document Type: Article

References (30)

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29. + (100).
30. sym=4.3%). The structure was solved by direct methods and refined anisotropically to R=6.8% (on F, 596 parameters, 3722 observed reflections above the 2σ background level) and Rw=19.8% (on intensities) with the SHELX93 program. Hydrogen atoms were introduced at their theoretical places with a fixed isotropic thermal factor U=0.05.The full description of the Xray structure of 10 has been deposited with the Cambridge Crystallography Data Centre, UK. A copy of the standard CIF output file can be obtained from the authors at the e-mail address : prange@lure.u-psud.fr