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Of seco-taxane

Taraboletti G, Gatto C, Riva A, et al. Anti-Angiogenic and Anti-Metastatic Activity of IDN 5390, a New C-Seco Taxane Derivative. Proceedings of the AACR, Vol. 42, March 2001. abstract 3162. [Pg.91]

Total synthesis of A-seco taxane was accomplished using aldol condensation route using Yb triflate as the catalyst [155],... [Pg.953]

Under oxidizing conditions (Jones reagent), taxol is converted to the 7-keto derivatives 20a and 20b (43) (see Scheme 3). Under these same conditions (2,11,28), the free 13-hydroxyl group of baccatin III (13b) and 10-deacetyl baccatin III (13a) is oxidized to form 13-oxobaccatin III (21b) and the deacetyl derivative (21a), respectively. Treatment of compound 20c, derived from the oxidation product 20a after protection of its 2 -hydroxyl group, with base leads to rearrangement products such as D-seco taxane 22. [Pg.205]


See other pages where Of seco-taxane is mentioned: [Pg.30]    [Pg.30]    [Pg.112]    [Pg.213]    [Pg.2799]    [Pg.2807]    [Pg.85]    [Pg.110]   
See also in sourсe #XX -- [ Pg.12 , Pg.179 , Pg.180 , Pg.201 ]

See also in sourсe #XX -- [ Pg.12 , Pg.179 , Pg.180 , Pg.201 ]




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Of taxane

Seco-taxane

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