Stereocontrolled Synthesis of Methyl αR,2S,3R-3-(l-Acetoxyethyl)-1- (4-methoxyphenyl)-4-oxoazetidine-2-carboxylate

Zoltán Madarász; Ildikó Németh; Paul Toscano; John Welch; József Nyitrai

doi:10.1016/0040-4039(95)01735-Z

Stereocontrolled Synthesis of Methyl αR,2S,3R-3-(l-Acetoxyethyl)-1- (4-methoxyphenyl)-4-oxoazetidine-2-carboxylate

Zoltán Madarász
, Ildikó Németh
, Paul Toscano
, John Welch
, József Nyitrai

Chemistry

University at Albany

Budapest University of Technology and Economics

Research output: Contribution to journal › Article › peer-review

5 Scopus citations

Abstract

A stereocontrolled synthesis of the key intermediates for 2-iso-oxa- and 2-isocephems is described. The absolute configuration of the title ester 8a is unambiguously determined by using X-ray analysis.

Original language	English
Pages (from-to)	8303-8306
Number of pages	4
Journal	Tetrahedron Letters
Volume	36
Issue number	45
DOIs	https://doi.org/10.1016/0040-4039(95)01735-Z
State	Published - Nov 6 1995

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@article{8de6975ebb4347c29a647ffdbaa8df96,

title = "Stereocontrolled Synthesis of Methyl αR,2S,3R-3-(l-Acetoxyethyl)-1- (4-methoxyphenyl)-4-oxoazetidine-2-carboxylate",

abstract = "A stereocontrolled synthesis of the key intermediates for 2-iso-oxa- and 2-isocephems is described. The absolute configuration of the title ester 8a is unambiguously determined by using X-ray analysis.",

author = "Zolt{\'a}n Madar{\'a}sz and Ildik{\'o} N{\'e}meth and Paul Toscano and John Welch and J{\'o}zsef Nyitrai",

year = "1995",

month = nov,

day = "6",

doi = "10.1016/0040-4039(95)01735-Z",

language = "English",

volume = "36",

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journal = "Tetrahedron Letters",

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TY - JOUR

T1 - Stereocontrolled Synthesis of Methyl αR,2S,3R-3-(l-Acetoxyethyl)-1- (4-methoxyphenyl)-4-oxoazetidine-2-carboxylate

AU - Madarász, Zoltán

AU - Németh, Ildikó

AU - Toscano, Paul

AU - Welch, John

AU - Nyitrai, József

PY - 1995/11/6

Y1 - 1995/11/6

N2 - A stereocontrolled synthesis of the key intermediates for 2-iso-oxa- and 2-isocephems is described. The absolute configuration of the title ester 8a is unambiguously determined by using X-ray analysis.

AB - A stereocontrolled synthesis of the key intermediates for 2-iso-oxa- and 2-isocephems is described. The absolute configuration of the title ester 8a is unambiguously determined by using X-ray analysis.

UR - https://www.scopus.com/pages/publications/0028892624

U2 - 10.1016/0040-4039(95)01735-Z

DO - 10.1016/0040-4039(95)01735-Z

M3 - Article

SN - 0040-4039

VL - 36

SP - 8303

EP - 8306

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 45

ER -

Stereocontrolled Synthesis of Methyl αR,2S,3R-3-(l-Acetoxyethyl)-1- (4-methoxyphenyl)-4-oxoazetidine-2-carboxylate

Abstract

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