Asymmetric Total Syntheses of Two 3-Acyl-5,6- dihydro-2H-pyrones: (R)-Podoblastin-S and (R)- Lachnelluloic Acid with Verification of the Absolute Configuration of (−)-Lachnelluloic Acid-Reference-Cited by-同舟云学术

Asymmetric Total Syntheses of Two 3-Acyl-5,6- dihydro-2H-pyrones: (R)-Podoblastin-S and (R)- Lachnelluloic Acid with Verification of the Absolute Configuration of (−)-Lachnelluloic Acid

Published:2017-01-01 Issue:1 Volume:22 Page:69
ISSN:1420-3049
Container-title:Molecules
language:en
Short-container-title:Molecules

Author:

Fujiwara Tetsuya,Tsutsumi Takeshi,Nakata Kohei,Nakatsuji Hidefumi,Tanabe Yoo^ORCID

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

Link

http://www.mdpi.com/1420-3049/22/1/69/pdf

Reference24 articles.

1. Naturally Occurring 6-Substituted 5,6-Dihydro-α-pyrones;Davies-Coleman,1989

2. Alternaric Acid, a Biologically Active Metabolic Product of the Fungus Alternaria solani

3. Structures and stereochemistries of new compounds related to alternaric acid

4. Total Synthesis and Stereochemistry of Alternaric Acid

5. Ruthenium-Catalyzed Alder Ene Type Reactions. A Formal Synthesis of Alternaric Acid

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