Asymmetric Synthesis of (+)-Galbelgin, (−)-Kadangustin J, (−)-Cyclogalgravin and (−)-Pycnanthulignenes A and B, Three Structurally Distinct Lignan Classes, Using a Common Chiral Precursor-Reference-Cited by-同舟云学术

Asymmetric Synthesis of (+)-Galbelgin, (−)-Kadangustin J, (−)-Cyclogalgravin and (−)-Pycnanthulignenes A and B, Three Structurally Distinct Lignan Classes, Using a Common Chiral Precursor

Published:2011-07-22 Issue:16 Volume:76 Page:6636-6648
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Rye Claire E.¹,Barker David¹

Affiliation:

1. School of Chemical Sciences, University of Auckland, Auckland, New Zealand

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo200968f

Reference38 articles.

1. An update on lignans: natural products and synthesis

2. An update on bioactive plant lignans

3. Stereoselective Synthesis of Tetrahydrofuran Lignans via BF3·OEt2-Promoted Reductive Deoxygenation/Epimerization of Cyclic Hemiketal: Synthesis of (−)-Odoratisol C, (−)-Futokadsurin A, (−)-Veraguensin, (+)-Fragransin A2, (+)-Galbelgin, and (+)-Talaumidin

4. Antifungal constituents from roots of Virolasurinamensis

5. Two lignans from Litsea grandis and L. gracilipes

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