Asymmetric synthesis of β-lactams and n-benzoyl-3-phenylisoserines via the staudinger reaction

Gunda I. Georg; Peter M. Mashava; Eyüp Akgün; Mark W. Milstead

doi:10.1016/S0040-4039(00)79708-5

Asymmetric synthesis of β-lactams and n-benzoyl-3-phenylisoserines via the staudinger reaction

Gunda I. Georg
, Peter M. Mashava
, Eyüp Akgün
, Mark W. Milstead

Medicinal Chemistry

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

65 Scopus citations

Abstract

Reaction of benzaldimine 5 derived from 2,3,4,6-tetra-O-acetyl-β-D-galactoseamine with acid chloride 6 yields cis β-lactam 7 as a single diastereoisomer. Hydrolysis of β-lactam 7 followed by N-benzoylation provides access toward N-benzoyl (2S,3R)-3-phenylisoserine 9. N-Benzoyl-3-phenylisoserines are important building blocks for the semi-synthesis of the anti-cancer agent taxol.

Original language	English (US)
Pages (from-to)	3151-3154
Number of pages	4
Journal	Tetrahedron Letters
Volume	32
Issue number	27
DOIs	https://doi.org/10.1016/S0040-4039(00)79708-5
State	Published - Jul 1 1991

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Copyright 2014 Elsevier B.V., All rights reserved.

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abstract = "Reaction of benzaldimine 5 derived from 2,3,4,6-tetra-O-acetyl-β-D-galactoseamine with acid chloride 6 yields cis β-lactam 7 as a single diastereoisomer. Hydrolysis of β-lactam 7 followed by N-benzoylation provides access toward N-benzoyl (2S,3R)-3-phenylisoserine 9. N-Benzoyl-3-phenylisoserines are important building blocks for the semi-synthesis of the anti-cancer agent taxol.",

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T1 - Asymmetric synthesis of β-lactams and n-benzoyl-3-phenylisoserines via the staudinger reaction

AU - Georg, Gunda I.

AU - Mashava, Peter M.

AU - Akgün, Eyüp

AU - Milstead, Mark W.

PY - 1991/7/1

Y1 - 1991/7/1

N2 - Reaction of benzaldimine 5 derived from 2,3,4,6-tetra-O-acetyl-β-D-galactoseamine with acid chloride 6 yields cis β-lactam 7 as a single diastereoisomer. Hydrolysis of β-lactam 7 followed by N-benzoylation provides access toward N-benzoyl (2S,3R)-3-phenylisoserine 9. N-Benzoyl-3-phenylisoserines are important building blocks for the semi-synthesis of the anti-cancer agent taxol.

AB - Reaction of benzaldimine 5 derived from 2,3,4,6-tetra-O-acetyl-β-D-galactoseamine with acid chloride 6 yields cis β-lactam 7 as a single diastereoisomer. Hydrolysis of β-lactam 7 followed by N-benzoylation provides access toward N-benzoyl (2S,3R)-3-phenylisoserine 9. N-Benzoyl-3-phenylisoserines are important building blocks for the semi-synthesis of the anti-cancer agent taxol.

UR - https://www.scopus.com/pages/publications/0025897103

UR - https://www.scopus.com/pages/publications/0025897103#tab=citedBy

U2 - 10.1016/S0040-4039(00)79708-5

DO - 10.1016/S0040-4039(00)79708-5

M3 - Article

AN - SCOPUS:0025897103

SN - 0040-4039

VL - 32

SP - 3151

EP - 3154

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 27

ER -

Asymmetric synthesis of β-lactams and n-benzoyl-3-phenylisoserines via the staudinger reaction

Abstract

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