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Lactones in foods

C 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   +2 more sources

Sesquiterpene lactone allergy

American Journal of Contact Dermatitis, 1996
Sesquiterpene lactones are a large, diverse group of chemicals found in several plant families that cause allergic contact dermatitis. The biological, botanical, allergenic, and structural significance of sesquiterpene lactones is explored as well as the clinical characteristics of cutaneous reactions.
E M, Warshaw, K A, Zug
openaire   +2 more sources

Synthesis of (+)-trans-Whisky Lactone, (-)-cis-Whisky Lactone, (+)-Cognac Lactone and (+)-Eldanolide

HETEROCYCLES, 1993
(+)-trans-Whisky lactone (5) and (-)-cis-whisky lactone (8), (+)-cognac lactone (9) and (+)-eldanolide (10) were synthesized starting from levoglucosenone (1) in optically pure ...
Takashi Ehata   +7 more
openaire   +1 more source

Preparation of lactones via tricarbonyliron–lactone complexes

J. Chem. Soc., Perkin Trans. 1, 1981
A number of tricarbonyliron–lactone complexes have been prepared from vinyl oxirans by treatment with pentacarbonyliron. In certain cases two η3-allyl complexes were isolated from a single vinyl oxiran. Oxidation of the complexes by cerium(IV) ammonium nitrate in acetonitrile leads predominantly to β-lactones.
Gary D. Annis   +3 more
openaire   +1 more source

Lactones 44. Microbial lactonization of γ-ketoacids

Journal of Molecular Catalysis B: Enzymatic, 2014
Abstract Enantiomerically pure γ-lactones ((+)-4a, (−)-5a, (+)-4b) have been obtained from the corresponding γ-ketoacids (3a and 3b) by their biotransformations with the three fungal strains: Rhodotorula glutinis AM242, Saccharomyces cerevisiae AM464 and Chaetomium sp. KCh6670.
Agnieszka Leśniak   +4 more
openaire   +1 more source

Lactone

1977
Walter Karrer   +2 more
openaire   +1 more source

ChemInform Abstract: CONVERSION OF LACTONE INTO LACTONE HEMITHIOACETAL AND SYNTHESIS OF ENOL LACTONE

Chemischer Informationsdienst, 1981
M. OCHIAI   +3 more
openaire   +1 more source

Unsaturated lactones

Chemistry of Heterocyclic Compounds, 1978
A. A. Avetisyan   +2 more
openaire   +1 more source

Lactones

2006
openaire   +1 more source

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