Results 141 to 150 of about 2,129 (203)
Mild ketyl radical generation and coupling with alkynes enabled by Cr catalysis: stereoselective access to E-exocyclic allyl alcohols. [PDF]
Chem SciLuo Z, Zhang X, Li Z, Luo M, Zeng X.
europepmc +1 more source
Descripteurs du caféier (Coffea spp. et Psilanthus spp.) [PDF]
, 2016 International Plant Genetic Resources Institute
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Nutritional, biochemical and health properties of Locust beans and its applications in the food industry: a review. [PDF]
J Food Sci TechnolNasrallah K +3 more
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Natural Product Reports, 2022
Carbocycle formation in the biosynthesis of the majority of cyclitols derived from carbohydrate origin are catalyzed by myo-inositol phosphate synthase (MIPS) family, dehydroquinate synthase (DHQS) family, radical SAM enzymes, and ribosyltransferase-isomerase type enzymes.
Fumitaka Kudo, Tadashi Eguchi
exaly +3 more sources
Carbocycle formation in the biosynthesis of the majority of cyclitols derived from carbohydrate origin are catalyzed by myo-inositol phosphate synthase (MIPS) family, dehydroquinate synthase (DHQS) family, radical SAM enzymes, and ribosyltransferase-isomerase type enzymes.
Fumitaka Kudo, Tadashi Eguchi
exaly +3 more sources
Angewandte Chemie International Edition in English, 1966
AbstractInformation has recently been obtained, mainly with the aid of radioactive compounds, about the biosynthesis of various cyclitols. It was found that the most widely occurring cyclitol, meso‐inositol, is biosynthesized by a pathway probably common to all organisms, in which the cyclohexane ring is formed by ring closure between the two terminal ...
H, Kindl +2 more
exaly +3 more sources
AbstractInformation has recently been obtained, mainly with the aid of radioactive compounds, about the biosynthesis of various cyclitols. It was found that the most widely occurring cyclitol, meso‐inositol, is biosynthesized by a pathway probably common to all organisms, in which the cyclohexane ring is formed by ring closure between the two terminal ...
H, Kindl +2 more
exaly +3 more sources
A Synthetic Cyclitol Glycoside
Nature, 1963THE synthesis of cyclitol glycosides is of interest because of the natural occurrence of these substances as such (galactinol) and as structural moieties of several antibiotics and phospholipids1,2. In this laboratory, attempts have been made to couple activated forms of glucose with protected derivatives3 of myo-inosamine-2 and, more recently ...
K A, CALDWELL +2 more
openaire +2 more sources
Cyclitols. XXXII. Cyclopentanepentols
Australian Journal of Chemistry, 1970Three cyclopentanepentols have been synthesized: the 1,2,4/3,5-isomer by acid hydrolysis of an anhydro-cyclopentanepentol, DL-1,2-anhydro-4,5-O-cyclohexylidene-1,2,3/4,5-cyclopentanepentol; the 1,2,3/4,5-isomer by deamination of (1,4/2,3,5)-5-amino-1,3-di-O-acetyl-2,3-O-cyclohexylidene-l,2,3,4-cycopentanetetrol; and the 1,2,3,4/5-isomer by solvolysis ...
SJ Angyal, BM Luttrell
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