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2,6-diisocyanatotoluene, conjugate diacid

 
National Institutes of Health

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2012
2012
The present study quantitatively analyses the gated photochromism and the acidity photomodulation properties of a diacid… Expand
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Highly Cited
2010
Highly Cited
2010
The synthesis of isosorbide aliphatic polyesters is demonstrated by the use of Novozym 435, a catalyst consisting of Candida… Expand
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2010
2010
Oxidative stress resulting from photosensitized ROS production in skin is widely accepted as the main contributor to the… Expand
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2007
2007
Upon dilution from a concentrated solution in dichloromethane, the diacid form of tetraphenylporphyrin {H(4)TPP(X)(2)} (X = Cl… Expand
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2007
2007
The nonlinear absorption of two porphyrin diacids (H4TPP2+ and H2DSP2+), the diprotonated forms of free base tetraphenylporphyrin… Expand
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2006
2006
Two novel isophthalic diacid-based monomers have been synthesized by inclusion in ring position 5 of a functionalized… Expand
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2006
2006
The formation of protein-decorated nanosized polymeric particles is described. Annexin-A5 protein binding to micellar aggregates… Expand
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2006
2006
[reaction: see text] Atropisomeric receptor 1 can change conformation and maintain the new conformation when heated and cooled in… Expand
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2000
2000
The total synthesis of the dimeric ellagitannin coriariin A is reported. The key reaction to access the dimeric framework was… Expand
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1988
1988
CS-622 is a prodrug type ACE inhibitor with a thiazepin ring. Its active form, CS-622 diacid, was slightly more potent than… Expand
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