Search alternatives:
step decrease » sizes decrease (Expand Search), teer decrease (Expand Search)
nm decrease » nn decrease (Expand Search), _ decrease (Expand Search), gy decreased (Expand Search)
we decrease » _ decrease (Expand Search), nn decrease (Expand Search), mean decrease (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
2 step » _ step (Expand Search), a step (Expand Search)
step decrease » sizes decrease (Expand Search), teer decrease (Expand Search)
nm decrease » nn decrease (Expand Search), _ decrease (Expand Search), gy decreased (Expand Search)
we decrease » _ decrease (Expand Search), nn decrease (Expand Search), mean decrease (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
2 step » _ step (Expand Search), a step (Expand Search)
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2076
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
Published 2007“…Four donor−acceptor [2]catenanes with cyclobis(paraquat-<i>p</i>-phenylene) (CBPQT<sup>4+</sup>) as the π-electron-accepting cyclophane and 1,5-dioxynaphthalene (DNP)-containing macrocyclic polyethers as π-electron donor rings have been synthesized under mild conditions, employing Cu<sup>+</sup>-catalyzed Huisgen 1,3-dipolar cycloaddition and Cu<sup>2+</sup>-mediated Eglinton coupling in the final steps of their syntheses. …”
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2077
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
Published 2007“…Four donor−acceptor [2]catenanes with cyclobis(paraquat-<i>p</i>-phenylene) (CBPQT<sup>4+</sup>) as the π-electron-accepting cyclophane and 1,5-dioxynaphthalene (DNP)-containing macrocyclic polyethers as π-electron donor rings have been synthesized under mild conditions, employing Cu<sup>+</sup>-catalyzed Huisgen 1,3-dipolar cycloaddition and Cu<sup>2+</sup>-mediated Eglinton coupling in the final steps of their syntheses. …”
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2078
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
Published 2007“…Four donor−acceptor [2]catenanes with cyclobis(paraquat-<i>p</i>-phenylene) (CBPQT<sup>4+</sup>) as the π-electron-accepting cyclophane and 1,5-dioxynaphthalene (DNP)-containing macrocyclic polyethers as π-electron donor rings have been synthesized under mild conditions, employing Cu<sup>+</sup>-catalyzed Huisgen 1,3-dipolar cycloaddition and Cu<sup>2+</sup>-mediated Eglinton coupling in the final steps of their syntheses. …”
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2079
Structural and Co-conformational Effects of Alkyne-Derived Subunits in Charged Donor−Acceptor [2]Catenanes
Published 2007“…Four donor−acceptor [2]catenanes with cyclobis(paraquat-<i>p</i>-phenylene) (CBPQT<sup>4+</sup>) as the π-electron-accepting cyclophane and 1,5-dioxynaphthalene (DNP)-containing macrocyclic polyethers as π-electron donor rings have been synthesized under mild conditions, employing Cu<sup>+</sup>-catalyzed Huisgen 1,3-dipolar cycloaddition and Cu<sup>2+</sup>-mediated Eglinton coupling in the final steps of their syntheses. …”
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2080
KYNA and zaprinast decrease the [Ca<sup>2+</sup>]i plateau phase following an IP3-mediated stimulus in mouse cortical astrocytes.
Published 2013“…<p><b>A</b>) A typical example of KYNA and zaprinast-induced decrease in somatic fluo-3 fluorescence time course measured in three different astrocytes in cultures: control (<i>upper panels</i>), in the presence of 10 μM KYNA (<i>middle panels</i>) or zaprinast 1 µM (<i>lower panels</i>). …”