Straightforward Asymmetric Entry to Highly Functionalized 3-Substituted 3-Hydroxy-β-lactams via Baylis−Hillman or Bromoallylation Reactions-Reference-Cited by-同舟云学术

Straightforward Asymmetric Entry to Highly Functionalized 3-Substituted 3-Hydroxy-β-lactams via Baylis−Hillman or Bromoallylation Reactions

Published:2004-01-13 Issue:3 Volume:69 Page:826-831
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Alcaide Benito¹,Almendros Pedro¹,Aragoncillo Cristina¹,Rodríguez-Acebes Raquel¹

Affiliation:

1. Departamento de Química Orgánica I, Facultad de Química, Universidad Complutense de Madrid, 28040-Madrid, Spain, and Instituto de Química Orgánica General, CSIC, Juan de la Cierva 3, 28006-Madrid, Spain

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo035472l

Reference31 articles.

1. The biosynthesis of tabtoxinine-beta-lactam. Use of specifically 13C-labeled glucose and 13C NMR spectroscopy to identify its biosynthetic precursors.

2. Kinetic mechanism of Escherichia coli glutamine synthetase

3. Glutamine Synthetase Inhibition: Possible Mode of Action of Wildfire Toxin from Pseudomonas tabaci

4. Sulfazecin and isosulfazecin, novel β-lactam antibiotics of bacterial origin

5. Preparation and alkylation of N-t-butyldimethylsilyl-3-trimethylsilyloxyazetidin-2-one

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