201856-57-7

Usage

Uses

Used in Pharmaceutical Industry:
(3R,4S)-tert-Butyl 3-(1-ethoxyethoxy)-2-oxo-4-phenylazetidine-1-carboxylate is used as a reagent in the synthesis of abeo-taxane derivatives, which are known for their broad inhibitory effects against the proliferation of various cancer cell lines, including colon cancer, melanoma, and renal cancer.
(3R,4S)-tert-Butyl 3-(1-ethoxyethoxy)-2-oxo-4-phenylazetidine-1-carboxylate is also used as a reagent in the synthesis of a novel D-ring modified Docetaxel (D494420) analogue. This analogue has demonstrated equipotent cytotoxicity in relation to Paclitaxel (P132500) towards cancer cell lines, indicating its potential as a therapeutic agent in cancer treatment.

InChI:InChI=1/C18H25NO5/c1-6-22-12(2)23-15-14(13-10-8-7-9-11-13)19(16(15)20)17(21)24-18(3,4)5/h7-12,14-15H,6H2,1-5H3

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 201856-48-6 (3R,4S)-3-<((R^*)-1'-ethoxyethyl)oxy>-4-phenyl-2-azetidinone 
• 132127-31-2 (3R,4S)-3-triisopropylsilyloxy-4-phenylazetidin-2-one 
• 132127-34-5 (3R,4S)-3-hydroxy-4-phenylazetidin-2-one 

Downstream Products

• 1116070-85-9 C₆₃H₇₃NO₁₉ 
• 1116070-88-2 2'-(1-ethoxyethyl)-docetaxel 
• 114915-20-7 Docetaxel 
• 1440522-38-2 C₄₇H₄₉NO₁₂ 
• 1440522-40-6 C₄₉H₅₃NO₁₄ 
• 1440522-39-3 C₄₅H₅₃NO₁₃ 
• 1440522-41-7 C₄₇H₅₇NO₁₅ 
• 1262663-17-1 C₄₉H₆₁NO₁₇ 
• 1262663-08-0 C₄₄H₅₁NO₁₄ 
• 1262663-07-9 C₄₄H₅₁NO₁₄ 
• 1262663-16-0 C₃₇H₄₇NO₁₂ 
• 1262663-15-9 C₃₇H₄₇NO₁₂ 
• 1195007-07-8 2'-EE-10-acetyl-7-Boc-docetaxel 
• 1195007-13-6 2'-EE-7,10-di-Boc-docetaxel 

Relevant academic research and scientific papers

A [...] he [...] synthesis process

A [...] he [...] synthesis process, in order to (3 R, 4 S) - 3 - hydroxy - 4 - phenyl - 2 - azetidinone as the starting material, adopts the one-pot synthesis, its first with vinyl ether condensation, with the BOC - anhydride is condensed directly [...] h

Anti-tumor compounds, pharmaceutical compositions, methods for preparation thereof and for treatment

The present invention is directed to novel taxanes useful as chemotherapeutic agents or their precursors. Processes for preparing the novel taxanes include coupling reactions, in the presence of a base, of baccatin of formula (III) or (IV) STR1 with β-lac

Anti-tumor compounds, pharmaceutical compositions, methods for preparation thereof and for treatment

The present invention is directed to novel taxanes useful as chemotherapeutic agents or their precursors. Processes for preparing the novel taxanes include coupling reactions, in the presence of a base, of baccatin of formula (III) or (IV) STR1 with β-lac

A highly efficient route to taxotere by the β-lactam synthon method

Taxotere, a highly promising anticancer drug, is synthesized through an efficient coupling of 7,10-diTroc-10-deacetylbaccatin III with enantiomerically pure (3R,4S)-1-tBOC-3-EEO- 4-phenylazetidin-2-one which is obtained via chiral ester enolate - imine cyclocondensation.