Results 281 to 290 of about 1,710,924 (336)
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New Synthesis of dl-sativene, dl-copacamphene, dl--sativenediol and dl-helminthosporal
Tetrahedron Letters, 1979Abstract Photocycloadducts from dl-piperitone and 1,1-dimethoxyethylene afforded bicyclo[3.2.1]oct-6-en-8-one derivatives under glc conditions in excellent yields. The synthesis of the title sesquiterpenes was accomplished using the bridged bicyclic compounds as intermediates.
Mitsutoshi Yanagiya +3 more
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DL-Lite: Practical Reasoning for Rich Dls. [PDF]
In this paper we study a DL rich enough to express UML class diagrams including ISA and disjointness between classes (but not covering constraints), typing of associations, and participation and functional cardinality constraints. For such a DL, which we
CALVANESE D. +4 more
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R-DLS: An Improved DLS Algorithm
2008 Seventh International Conference on Grid and Cooperative Computing, 2008As dynamic-level scheduling algorithm does not consider the risk taken by resource nodes and users' demand, it proposes an analytic hierarchy process approach (AHP) based improved DLS algorithm. By such AHP approach, it manages the task provided by users, and obtains the weight value which reflects users' demand.
Xiaoqian Liu +3 more
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Vibrational spectral analysis of dl-valine dl-valinium and dl-methionine dl-methioninium picrates
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2006A comparative study of infrared and Raman spectra of DL-valine DL-valinium picrate (DL-VVP) and DL-methionine DL-methioninium picrate (DL-MMP) at the room temperature in 4000-50 cm(-1) range helps to determine the effect of hydrogen bonds in these crystals.
M Briget, Mary +2 more
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Stereospecific synthesis of dl-cyclopenin and dl-cyclopenol
Tetrahedron, 1970Abstract A stereospecific synthesis of dl -cyclopenin ( 1 ) is described corroborating previous structural and stereochemical assignments. The hippuric acid 10 was converted to cis ester 11 which was reduced and cyclized separately to cis and trans 3-benzylidene-4-methyl-1- H -1,4-benzodiazepin-2,5-diones 12 and 14 .
J D, White +2 more
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Antioxidants and Redox Signaling, 2019
Aims: Oxidative stress and neuroinflammation play important roles in the pathology of Alzheimer's disease (AD). Thioredoxin-interacting protein (TXNIP), an endogenous inhibitor of antioxidant thioredoxin, is suspected to be an important modulator of ...
Chun-Yan Wang +5 more
semanticscholar +1 more source
Aims: Oxidative stress and neuroinflammation play important roles in the pathology of Alzheimer's disease (AD). Thioredoxin-interacting protein (TXNIP), an endogenous inhibitor of antioxidant thioredoxin, is suspected to be an important modulator of ...
Chun-Yan Wang +5 more
semanticscholar +1 more source
Dl-3-n-Butylphthalide (NBP): A Promising Therapeutic Agent for Ischemic Stroke.
CNS and Neurological Disorders - Drug Targets, 2018BACKGROUND AND OBJECTIVE Stroke is a leading cause of morbidity and mortality in both developed and developing countries all over the world. The only drug for ischemic stroke approved by FDA is recombinant tissue plasminogen activator (rtPA).
Shan Wang +8 more
semanticscholar +1 more source
Computer Physics Communications, 2001
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zbMATH Open Web Interface contents unavailable due to conflicting licenses.
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Justus Liebigs Annalen der Chemie, 1958
Abstract1) Aus Carbobenzoxy‐Dl‐seryl‐Dl‐alanyl‐glycin‐azid und Glycyl‐Dl‐alanyl‐glycin‐benzylester wurden die Carbobenzoxy‐hexapeptid‐benzylester synthetisiert und durch fraktionierte Kristallisation nach katalytischer Hydrierung die vier Racemate A, B, C und D von Dl‐alanyl‐glycyl‐glycyl‐Dl‐alanyl‐glycin erhalten.—2) Zwei Racemate A und B des ...
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Abstract1) Aus Carbobenzoxy‐Dl‐seryl‐Dl‐alanyl‐glycin‐azid und Glycyl‐Dl‐alanyl‐glycin‐benzylester wurden die Carbobenzoxy‐hexapeptid‐benzylester synthetisiert und durch fraktionierte Kristallisation nach katalytischer Hydrierung die vier Racemate A, B, C und D von Dl‐alanyl‐glycyl‐glycyl‐Dl‐alanyl‐glycin erhalten.—2) Zwei Racemate A und B des ...
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Helvetica Chimica Acta, 1975
AbstractA synthetic approach to a variety of monomeric Vinca alkaloids is described. The sequence involves, among its crucial phases, the generation of appropriate nine‐membered ring intermediates which are then elaborated via a transannular cyclization approach to the desired natural products.
J P, Kutney +7 more
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AbstractA synthetic approach to a variety of monomeric Vinca alkaloids is described. The sequence involves, among its crucial phases, the generation of appropriate nine‐membered ring intermediates which are then elaborated via a transannular cyclization approach to the desired natural products.
J P, Kutney +7 more
openaire +2 more sources

