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  General strategy for the synthesis of B-1 phytoprostanes, dinor isoprostanes, and analogs

Schmidt, A., & Boland, W. (2007). General strategy for the synthesis of B-1 phytoprostanes, dinor isoprostanes, and analogs. Journal of Organic Chemistry, 72(5), 1699-1706. doi:10.1021/jo062359x.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-0012-A328-4 Version Permalink: https://hdl.handle.net/21.11116/0000-0009-35F1-B
Genre: Journal Article

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 Creators:
Schmidt, A.1, 2, Author           
Boland, W.1, Author           
Affiliations:
1Department of Bioorganic Chemistry, MPI for Chemical Ecology, Max Planck Society, ou_24028              
2IMPRS on Ecological Interactions, MPI for Chemical Ecology, Max Planck Society, Jena, DE, ou_421900              

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Free keywords: Plants Prostaglandins Metabolism Oxidation Acids f-1 Chemistry & Analysis in Current Contents(R)/Life Sciences Organic Chemistry/Polymer Science in Current Contents(R)/Physical, Chemical & Earth Sciences
 Abstract: The synthesis of the phytoprostane B-1 types I and II is achieved in high overall yield (35-53%) by only two principal transformations starting from 1,3-cyclopentanedione. The first side chain is attached via O-acylation of the 1,3-dione followed by rea

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 Dates: 2007
 Publication Status: Issued
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 Identifiers: Other: BOL406
DOI: 10.1021/jo062359x
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Title: Journal of Organic Chemistry
Source Genre: Journal
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Pages: - Volume / Issue: 72 (5) Sequence Number: - Start / End Page: 1699 - 1706 Identifier: -