نتایج جستجو برای: chemoenzymatic

تعداد نتایج: 829  

Journal: :Bioscience, Biotechnology, and Biochemistry 2021

Abstract Prunetin (4′,5-dihydroxy-7-methoxyisoflavone) was semisynthesized in 8 steps from readily available naringenin 26% total yield. The key reaction chemoenzymatic sequential deacetylation to 6′-acetoxy-2′,4″-dihydroxy-4′-methoxychalcone, the situ-formed precursor for thallium(III) nitrate-mediated oxidative rearrangement.

2012
Oscar Cascón Sabrina Touchet David J. Miller Veronica Gonzalez Juan A. Faraldos Rudolf K. Allemann

Terpenoids represent a valuable class of bioactive fine chemicals and are therefore attractive targets for synthetic modification; modulation of their natural properties may lead to new medicinal and agrochemical compounds with improved properties. However, the complexity of the hydrocarbon skeletons and the often significant chemical instability of many terpenoids can present a formidable chal...

Journal: :Current Protocols in Nucleic Acid Chemistry 2004

Journal: :Journal of the American Chemical Society 2019

Journal: :Bioscience, Biotechnology, and Biochemistry 1992

Journal: :Organic & biomolecular chemistry 2009
Marloes A Wijdeven Rutger J F van den Berg Roel Wijtmans Peter N M Botman Richard H Blaauw Hans E Schoemaker Floris L van Delft Floris P J T Rutjes

Two complementary strategies for the synthesis of febrifugine are detailed based on previously developed chemoenzymatic approaches to the 3-hydroxypiperidine skeleton. The introduction of the quinazolone-containing side chain in both strategies was based on an N-acyliminium ion-mediated coupling reaction.

Journal: :Molecules 2018
Theodore Tyrikos-Ergas Vasileios Giannopoulos Ioulia Smonou

Rugulactone is a natural product isolated from the plant Cryptocarya rugulosa. It has shown very important biological activity as an inhibitor of the nuclear factor κB (NF-κB) activation pathway. A new chemoenzymatic approach towards the synthesis of rugulactone is presented here. The chirality, induced to the key intermediate by a stereoselective enzymatic reduction utilizing NADPH-dependent k...

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