Total Synthesis of Marinomycins A−C and of Their Monomeric Counterparts Monomarinomycin A and iso-Monomarinomycin A-Reference-Cited by-同舟云学术

Total Synthesis of Marinomycins A−C and of Their Monomeric Counterparts Monomarinomycin A and iso-Monomarinomycin A

Published:2007-01-24 Issue:6 Volume:129 Page:1760-1768
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Nicolaou K. C.¹,Nold Andrea L.¹,Milburn Robert R.¹,Schindler Corinna S.¹,Cole Kevin P.¹,Yamaguchi Junichiro¹

Affiliation:

1. Contribution from the Department of Chemistry and The Skaggs Institute for Chemical Biology, The Scripps Research Institute, 10550 North Torrey Pines Road, La Jolla, California 92037, and the Department of Chemistry and Biochemistry, University of California, San Diego, 9500 Gilman Drive, La Jolla, California 92093

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja068053p

Reference30 articles.

1. Bioactive Microbial Metabolites

2. Platensimycin is a selective FabF inhibitor with potent antibiotic properties

3. Marine actinomycete diversity and natural product discovery

4. Salinosporamide A: A Highly Cytotoxic Proteasome Inhibitor from a Novel Microbial Source, a Marine Bacterium of the New Genus Salinospora

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