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2000
Volume 7, Issue 6
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

A novel protocol for the semi-synthesis of docetaxel was achieved in four steps from 10-deacetyl baccatin III with an overall yield of 50%. The key step is the selective protection of the C(7) and C(10) hydroxyl groups of 10- deacetyl baccatin III, utilizing benzyl chloromate as a selective protecting reagent, which are capable of being conveniently removed by Pd/C under hydrogen atmosphere.

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/content/journals/loc/10.2174/157017810791824892
2010-09-01
2025-10-03
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/content/journals/loc/10.2174/157017810791824892
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  • Article Type:
    Research Article
Keyword(s): 10-DAB III; benzyl chloromate; Docetaxel; semi-synthesis
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