Synthesis of Strained 1,3-Diene Macrocycles via Copper-Mediated Castro–Stephens Coupling/Alkyne Reduction Tandem Reactions-Reference-Cited by-同舟云学术

Synthesis of Strained 1,3-Diene Macrocycles via Copper-Mediated Castro–Stephens Coupling/Alkyne Reduction Tandem Reactions

Published:2015-07-15 Issue:15 Volume:17 Page:3902-3905
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Li Wei¹,Schneider Christopher M.²,Georg Gunda I.¹

Affiliation:

1. Department of Chemistry, Department of Medicinal Chemistry, and the Institute for Therapeutics Discovery and Development, University of Minnesota, 717 Delaware Street SE, Minneapolis, Minnesota 55414, United States

2. Department of Medicinal Chemistry, University of Kansas, 1251 Wescoe Hall Drive, Lawrence, Kansas 66045, United States

Funder

Vince and McKnight Endowed Chairs, University of Minnesota

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b01892

Reference51 articles.

1. The exploration of macrocycles for drug discovery — an underexploited structural class

2. Natural products in drug discovery

3. Macrocycles in new drug discovery

4. Natural product and natural product derived drugs in clinical trials

5. Macrocycles Are Great Cycles: Applications, Opportunities, and Challenges of Synthetic Macrocycles in Drug Discovery

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