Radical-Triggered Tandem Cyclization of 1,6-Enynes with H2O: A Way to Access Strained 1H-Cyclopropa[b]naph thalene-2,7-diones-Reference-Cited by-同舟云学术

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Radical-Triggered Tandem Cyclization of 1,6-Enynes with H2O: A Way to Access Strained 1H-Cyclopropa[b]naph thalene-2,7-diones

Published:2018-10-25 Issue:22 Volume:20 Page:7053-7056
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Zheng Limeng¹,Zhou Bingwei¹,Jin Hongwei¹,Li Ting²^ORCID,Liu Yunkui¹^ORCID

Affiliation:

1. State Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology, Zhejiang University of Technology, Hangzhou, 310014, P. R. China

2. College of Chemistry and Pharmaceutical Engineering, Nanyang Normal University, Nangyang, Henan 473061, P. R. China

Funder

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.8b03007

Reference67 articles.

1. Total synthesis of natural ambruticin

2. Synthesis of cyclopropane containing natural products

3. Callipeltoside A: Assignment of Absolute and Relative Configuration by Total Synthesis We thank the National Science Foundation and the National Institutes of Health for their generous support of our programs. OD was supported in part by a fellowship from the Association pour la Recherche contre le Cancer (ARC). J.L.G. was supported in part by a NIH postdoctoral fellowship from the National Cancer Institute. Mass spectra were provided by the Mass Spectroscopy Facility at the University of California, San Francisco supported by the NIH Division of Research Resources, and the Mass Spectrometry Facility at University of California, Irvine. We thank Dr. John Greaves of the latter facility for his assistance.

4. Biosynthesis and Metabolism of Cyclopropane Rings in Natural Compounds

5. Synthesis and Properties of Cyclopropane-Derived Peptidomimetics

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