Studies in Polyphenol Chemistry and Bioactivity. 3.1,2 Stereocontrolled Synthesis of Epicatechin-4α,8-epicatechin, an Unnatural Isomer of the B-Type Procyanidins-Reference-Cited by-同舟云学术

Studies in Polyphenol Chemistry and Bioactivity. 3.1,2 Stereocontrolled Synthesis of Epicatechin-4α,8-epicatechin, an Unnatural Isomer of the B-Type Procyanidins

Published:2001-01-31 Issue:4 Volume:66 Page:1287-1296
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Kozikowski Alan P.¹,Tückmantel Werner¹,Hu Youhong¹

Affiliation:

1. Georgetown University Medical Center, Drug Discovery Program, 3900 Reservoir Road NW, Washington, DC 20007

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo001462y

Reference23 articles.

1. Studies in Polyphenol Chemistry and Bioactivity. 1. Preparation of Building Blocks from (+)-Catechin. Procyanidin Formation. Synthesis of the Cancer Cell Growth Inhibitor, 3-O-Galloyl-(2R,3R)-epicatechin-4β,8-[3-O-galloyl-(2R,3R)-epicatechin]

2. Studies in Polyphenol Chemistry and Bioactivity. 2.1 Establishment of Interflavan Linkage Regio- and Stereochemistry by Oxidative Degradation of an O-Alkylated Derivative of Procyanidin B2 to (R)-(−)-2,4-Diphenylbutyric Acid

3. A novel pyrogallol A-ring proanthocyanidin dimer from Acacia melanoxylon

4. Procyanidin polymers of Douglas fir bark: Structure from degradation with phloroglucinol

5. Acid-catalyzed rearrangements of flavan-4-phloroglucinol derivatives to novel 6-hydroxyphenyl-6a,11b-dihydro-6H-[1]benzofuro[2,3-c] chromenes and hydroxyphenyl-3,2′-spirobi[dihydro[1]benzofurans]

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