Asymmetric [C + NC + CC] Coupling Entry to the Naphthyridinomycin Natural Product Family: Formal Total Synthesis of Cyanocycline A and Bioxalomycin β2-Reference-Cited by-同舟云学术

Asymmetric [C + NC + CC] Coupling Entry to the Naphthyridinomycin Natural Product Family: Formal Total Synthesis of Cyanocycline A and Bioxalomycin β2

Published:2011-05-31 Issue:13 Volume:76 Page:5283-5294
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Garner Philip,Kaniskan H. Ümit¹,Keyari Charles M.²,Weerasinghe Laksiri²

Affiliation:

1. Department of Chemistry, Case Western Reserve University, Cleveland, Ohio 44106-7078, United States

2. Department of Chemistry, Washington State University, Pullman, Washington 99164-4630, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo200553g

Reference47 articles.

1. Cyanonaphthyridinomycin: a derivative of naphthyridinomycin.

2. Cyanocycline A, a new antibiotic taxonomy of the producing organism, fermentation, isolation and characterization.

3. New Cyanocyclines from a Cyanide-Treated Broth of Streptomyces lusitanus

4. New semisynthetic antitumor antibiotics, SF-1739 HP and naphthocyanidine.

5. Dnacins, new antibiotics. I. Producing organism, fermentation, and antimicrobial activities.

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