Solid-Phase Synthesis of β-Lactams via the Miller Hydroxamate Approach-Reference-Cited by-同舟云学术

Solid-Phase Synthesis of β-Lactams via the Miller Hydroxamate Approach

Published:2001-01-13 Issue:3 Volume:3 Page:337-340
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Meloni Marco Massimiliano¹,Taddei Maurizio¹

Affiliation:

1. Dipartimento di Chimica, Università degli Studi di Sassari, Via Vienna 2, I-07100 Sassari, Italy

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol006779z

Reference16 articles.

1. β-Lactam Derivatives as Inhibitors of Human Cytomegalovirus Protease

2. Solid-Supported Combinatorial Synthesis of Structurally Diverse β-Lactams

3. Small ring constrained peptidomimetics. Synthesis of aziridine parallel β-sheet mimetics

4. For a comprehensive review on the possible synthetic approaches to azetidinones see: Perrone, E.; Franceschi, G. InRecent Progress in theChemical Synthesis of Antibiotics; Lukacs, G., Ohno, M., Eds.; Springer-Verlag: Berlin, 1990; p 613.

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