Results 11 to 20 of about 95,231 (345)

Studies on Phenolic Lactones

open access: bronzeBulletin of the Agricultural Chemical Society of Japan, 1959
α-Exo-unsaturated-γ-butyrolactones were prepared. Reduction of α-benzylidene succinic acid esters with lithium aluminum hydride afford 2-benzylidene-1,4-butanediols. Manganese dioxide oxidation of glycols followed by silver oxide oxidation and lactonization afford α-benzylidene-γ-butyrolactones. Thus α-benzylidene-, α-anisylidene-, α-veratrylidene-, α-(
Kyôhei Yamashita, Masanao Matsui
openalex   +9 more sources

Structure of Mokko Lactone and Dehydrocostus Lactone

open access: bronzeChemical and Pharmaceutical Bulletin, 1964
Hiroshi Hikino   +3 more
openalex   +5 more sources

Microbial Reduction of Ketopantoyl Lactone to Pantoyl Lactone [PDF]

open access: yesApplied Microbiology, 1974
The results of a microbial survey study have shown that the ability to reduce added ketopantoic acid (or ketopantoyl lactone) and accumulate pantoic acid (or pantoyl lactone) in the growth medium is widespread among diverse fungi. The reductions generally proceeded with less than full stereoselectivity.
Dorothy G. Bradley   +2 more
openaire   +2 more sources

A C-to-B Atom Swap on Coumarins and Dibenzolactones. [PDF]

open access: yesAngew Chem Int Ed Engl
Cyclic boronic hemiesters, boron isosteres of lactones, display unique and valuable chemical properties. Herein, we report a novel method for their synthesis via nickel‐catalyzed decarbonylative borylation, enabled by electron‐rich phosphine ligands to achieve a formal “C‐to‐B” atom swap.
You T, Luu QH, Li J.
europepmc   +3 more sources

Antimicrobial Activity of Lactones

open access: yesAntibiotics, 2022
The development of bacterial resistance to antibiotics and the consequent lack of effective therapy is one of the biggest problems in modern medicine. A consequence of these processes is an urgent need to continuously design and develop novel antimicrobial agents. Among the compounds showing antimicrobial potential, lactones are a group to explore. For
Marcelina Mazur, Dorota Masłowiec
openaire   +3 more sources

Syntheses of Unsaturated Lactones

open access: bronzeAgricultural and Biological Chemistry, 1969
6-Pentyl-α-pyrone, 6-propyl-α-pyrone and 4-decenoic acid-δ-lactone were prepared, and the nature of their flavors was investigated. Unsaturated lactones having the best flavorous nature as a butter or butter cake flavor among the lactones having double bond at various site, were 2-ene-δ-lactones which have a double bond at the α-position of the lactone
Akio NOBUHARA
openalex   +7 more sources

Contribution of microscopy for understanding the mechanism of action against trypanosomatids [PDF]

open access: yes, 2018
Transmission electron microscopy (TEM) has proved to be a useful tool to study the ultrastructural alterations and the target organelles of new antitrypanosomatid drugs.
A Martinez-Palomo   +90 more
core   +1 more source

Lactones in foods

open access: yesC R C Critical Reviews in Food Science and Nutrition, 1976
Lactones represent another important class of flavor compounds that have been found in a wide variety of foods although traditionally they have been mainly associated with dairy products. This review summarizes their occurrences in foods along with their formation pathways, sensory properties, and isolation, identification, and synthesis techniques ...
Joseph A. Maga, Ira Katz
openaire   +3 more sources

Synthesis and Cytotoxic Activity of Some 3-Benzyl-5-Arylidenefuran-2(5H)-ones

open access: yesMolecules, 2007
3-Benzyl-furan-2(5H)-one (2a) and 3-(4-bromobenzyl)-furan-2(5H)-one (2b) were treated with TBDMSOTf and converted into the corresponding tert-butyldimethyl-silylfuran ethers.
Manoel Odorico Moraes   +7 more
doaj   +1 more source

Synthesis of spiroacetals using functionalised titanium carbenoids [PDF]

open access: yes, 2008
Alkylidenation of lactones with functionalised titanium carbenoid reagents (Schrock carbenes) followed by acid-induced cyclisation of the resulting enol ethers constitutes a new method for the preparation of [4.4], [4.5] and [5.5] spiroacetals (1,6 ...
Aho   +52 more
core   +1 more source

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