Issue 4, 1997
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Synthesis and NMR studies of key intermediates to a new class of β-lactam: the trinems

Carla Marchioro,   Giorgio Pentassuglia,   Alcide Perboni  and  Daniele Donati  

Abstract

An efficient synthesis of the four isomeric epoxides 4a–d, key compounds to the trinem ring system, starting from (3R,4R,1′R)-(+)-4-acetoxy-3-[1′- (tert-butyldimethylsilyloxy)ethyl]azetidin-2-one 6a is described. All the intermediates have been characterized by means of NMR techniques.

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Article information

DOI
https://doi.org/10.1039/A605081F
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1997, 463-468

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Synthesis and NMR studies of key intermediates to a new class of β-lactam: the trinems

C. Marchioro, G. Pentassuglia, A. Perboni and D. Donati, J. Chem. Soc., Perkin Trans. 1, 1997, 463 DOI: 10.1039/A605081F

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