Lead tetraeetate oxidation of 6u-hydmxy-7-epi-paclitaxel leads to C-.or-paclitaxel and C-seco-paclitaxel derivatives. Tetrapropylammonium perruthenate (TPAP) oxidation of a 6tx-hydroxy-7-epi-paclitaxel derivative leads to a 6-formyl-C-nor-paclitaxel derivative. Reaction of a 6ot-O-trifluoromethanesu
Synthesis and biological evaluation of C-3′NH/C-10 and C-2/C-10 modified paclitaxel analogues
✍ Scribed by Erkan Baloglu; Jeannine M Hoch; Sabarni K Chatterjee; Rudravajhala Ravindra; Susan Bane; David G.I Kingston
- Book ID
- 108479303
- Publisher
- Elsevier Science
- Year
- 2003
- Tongue
- English
- Weight
- 272 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0968-0896
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📜 SIMILAR VOLUMES
AbstractÐStructure modi®cation of paclitaxel at the C-6 and C-7 positions has been achieved using the readily available intermediate 6ahydroxy-7-epipaclitaxel (2). While a single diastereomer of the cyclic sul®te of 2 was prepared at lower temperature, both diastereomers were obtained at room temper
Starting from 7,9-diTes-10-dehydro C-secobaccatin Ili (4a), C-seco analogues of paclitaxel retaining biological activity were synthesised.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v