Studies on the Stereostructure of Eudesmanolides from Umbelliferae: Total Synthesis of (+)-Decipienin A-Reference-Cited by-同舟云学术

Studies on the Stereostructure of Eudesmanolides from Umbelliferae: Total Synthesis of (+)-Decipienin A

Published:2000-05 Issue:21 Volume:56 Page:3409-3414
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Macı́as Francisco A.,Aguilar José Marı́a,Molinillo José Marı́a G.,Rodrı́guez-Luı́s Francisco,Collado Isidro G.,Massanet Guillermo M.,Fronczek Frank R.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

1. Progress in the Chemistry of Organic Natural Products;Fischer,1979

2. Biological activities of sesquiterpene lactones

3. Phytochemistry of Medicinal Plants;Marles,1995

4. Sesquiterpene lactones of the umbelliferae

5. Studies on the stereostructure of eudesmanolides from Umbelliferae: synthesis of 11β-angeloyloxy-α-santonin

Cited by 24 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Identification and characterization of an ene-reductase from Corynebacterium casei;International Journal of Biological Macromolecules;2024-04

2. Whole-cell biocatalyzed organic solvent-free conversion of dill oil to cis-(-)-dihydrocarvone rich aromatic hydrosol: Chemical and aroma profiling;Process Biochemistry;2022-11

3. Semi‐rational protein engineering of a novel ene‐reductase from Galdieria sulphuraria for asymmetric reduction of ( R )‐carvone and ketoisophorone;Biotechnology and Applied Biochemistry;2022-08-11

4. Recent syntheses and biological profiling of quassinoids;Organic & Biomolecular Chemistry;2022

5. Value Addition to Chemical Compounds Through Biotransformation;Industrial Microbiology and Biotechnology;2022