Cycloreversion of β-lactams via photoinduced electron transfer-Reference-Cited by-同舟云学术

Cycloreversion of β-lactams via photoinduced electron transfer

Published:2014 Issue:42 Volume:12 Page:8428-8432
ISSN:1477-0520
Container-title:Org. Biomol. Chem.
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Pérez-Ruiz Raúl¹²³,Sáez Jose A.¹²³,Jiménez M. Consuelo¹²³,Miranda Miguel A.¹²³

Affiliation:

1. Departamento de Química/Instituto de Tecnología Química UPV-CSIC

2. Universitat Politécnica de València

3. Valencia, Spain

Abstract

With DABCO as an electron donor, photoinduced cycloreversion of β-lactams leads to olefins through 1,4-radical anions and 1,4-biradicals as intermediates.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/OB/C4OB01416B

Reference31 articles.

1. Antibacterial Natural Products in Medicinal Chemistry—Exodus or Revival?

2. β-Lactams in the New Millennium. Part-I: Monobactams and Carbapenems

3. β-Lactams in the New Millennium. Part-II: Cephems, Oxacephems, Penams and Sulbactam

4. The Discovery and Development of Modified Penicillin- and Cephalosporin- Derived β-Lactamase Inhibitors

5. Design of β-Lactams with Mechanism Based Nonantibacterial Activities

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