Stereoselective Synthesis of Acortatarins A and B-Reference-Cited by-同舟云学术

Stereoselective Synthesis of Acortatarins A and B

Published:2012-08-27 Issue:17 Volume:14 Page:4442-4445
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Wurst Jacqueline M.¹,Verano Alyssa L.¹,Tan Derek S.¹

Affiliation:

1. Tri-Institutional Training Program in Chemical Biology, Pharmacology Program−Weill Cornell Graduate School of Medical Sciences, Molecular Pharmacology & Chemistry Program, and Tri-Institutional Research Program, Memorial Sloan−Kettering Cancer Center, 1275 York Avenue, Box 422, New York, New York 10065, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol3019456

Reference43 articles.

1. Acortatarins A and B, Two Novel Antioxidative Spiroalkaloids with a Naturally Unusual Morpholine Motif from Acorus tatarinowii

2. Pollenopyrroside A and B, Novel Pyrrole Ketohexoside Derivatives from Bee-Collected Brassica campestris Pollen

3. Free radicals and antioxidants in normal physiological functions and human disease

4. Total Synthesis and Stereochemical Revision of Acortatarins A and B

5. A Convergent Synthesis of the 2-Formylpyrrole Spiroketal Natural Product Acortatarin A

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