Synthesis of a conformationally restricted analogue of paclitaxel

Luciano Barboni; Catia Lambertucci; Roberto Ballini; Giovanni Appendino; Ezio Bombardelli

doi:10.1016/S0040-4039(98)01537-8

Synthesis of a conformationally restricted analogue of paclitaxel

Luciano Barboni, Catia Lambertucci, Roberto Ballini, Giovanni Appendino, Ezio Bombardelli

Risultato della ricerca: Contributo su rivista › Articolo in rivista › peer review

Abstract

A conformationally constrained analogue of the paclitaxel side-chain was synthesised in an enantioselective way from ethyl 1H-indene-2-carboxylate. Coupling with 7-triethylsilylbaccatin III and deprotection afforded 2',2''- methylenepaclitaxel, a novel analogue of the natural product retaining anticancer activity.

Lingua originale	Inglese
pagine (da-a)	7177-7180
Numero di pagine	4
Rivista	Tetrahedron Letters
Volume	39
Numero di pubblicazione	39
DOI	https://doi.org/10.1016/S0040-4039(98)01537-8
Stato di pubblicazione	Pubblicato - 24 set 1998
Pubblicato esternamente	Sì

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10.1016/S0040-4039(98)01537-8

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title = "Synthesis of a conformationally restricted analogue of paclitaxel",

abstract = "A conformationally constrained analogue of the paclitaxel side-chain was synthesised in an enantioselective way from ethyl 1H-indene-2-carboxylate. Coupling with 7-triethylsilylbaccatin III and deprotection afforded 2',2''- methylenepaclitaxel, a novel analogue of the natural product retaining anticancer activity.",

author = "Luciano Barboni and Catia Lambertucci and Roberto Ballini and Giovanni Appendino and Ezio Bombardelli",

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AU - Barboni, Luciano

AU - Lambertucci, Catia

AU - Ballini, Roberto

AU - Appendino, Giovanni

AU - Bombardelli, Ezio

PY - 1998/9/24

Y1 - 1998/9/24

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AB - A conformationally constrained analogue of the paclitaxel side-chain was synthesised in an enantioselective way from ethyl 1H-indene-2-carboxylate. Coupling with 7-triethylsilylbaccatin III and deprotection afforded 2',2''- methylenepaclitaxel, a novel analogue of the natural product retaining anticancer activity.

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U2 - 10.1016/S0040-4039(98)01537-8

DO - 10.1016/S0040-4039(98)01537-8

M3 - Article

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JO - Tetrahedron Letters

JF - Tetrahedron Letters

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Synthesis of a conformationally restricted analogue of paclitaxel

Abstract

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