An Efficient Chemoenzymatic Strategy for the Synthesis of Wild-Type and Vancomycin-Resistant Bacterial Cell-Wall Precursors: UDP-N-acetylmuramyl-peptides-Reference-Cited by-同舟云学术

An Efficient Chemoenzymatic Strategy for the Synthesis of Wild-Type and Vancomycin-Resistant Bacterial Cell-Wall Precursors: UDP-N-acetylmuramyl-peptides

Published:2001-09-14 Issue:40 Volume:123 Page:9916-9917
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Liu Haitian¹,Sadamoto Reiko¹,Sears Pamela S.¹,Wong Chi-Huey¹

Affiliation:

1. Department of Chemistry and the Skaggs Institute for Chemical Biology The Scripps Research Institute 10550 North Torrey Pines Road La Jolla, California 92037

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja011708w

Reference9 articles.

1. The Crisis in Antibiotic Resistance

2. The First Total Synthesis of Bacterial Cell Wall Precursor UDP−N-Acetylmuramyl-Pentapeptide (Park Nucleotide)

3. 1H-Tetrazole as Catalyst in Phosphomorpholidate Coupling Reactions: Efficient Synthesis of GDP-Fucose, GDP-Mannose, and UDP-Galactose

4. Substrate Synthesis and Activity Assay for MurG

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