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Guamdimum-based receptors

Guan s supramolecular triblock copolymers with binding sites localized within soft, microphase-segregated domains, Self-healing of a triblock after cutting and healing at 45 C. Adopted with permission from . Copyright 2012 John Wiley Sons, Inc.

Guan s synthesis of a biomimetic linear modular polymer. Reprinted with permission from . Copyright 2009 American Chemical Society

Guanabenz lowers blood pressure by stimulating the central alpha2-adrenergic receptor, decreasing

Guanacastepenes produced by endophytic fungi from Daphnopsis amercina

Guanidine 13 mediated asymmetric azidation of l-indanol

Guanidine analogue with SMe or Me.

Guanidine catalysed formation of oxazolidinone and oxazole ring systems

Guanidine catalysed hydrolysis of RNA

Guanidine catalysed Strecker reaction

Guanidine catalyzed phospha-Michael addition on nitroolefins.

Guanidine compounds as Brpnsted base catalysts

Guanidine denaturation of apolipoprotein E as assessed by circular dichroism. The molar ellipticity .

Guanidine derivatives. Arginine degradation in a mushroom. TA transamidination, Arg i-ar-ginine, Orn L-ornithine.

Guanidine derivatives. Different types of guanidine derivatives.

Guanidine derivatives. Metaboiic fates of arginine. TA transamidination. 272

Guanidine HCI-induced unfolding of wild-type iso-1-cytochrome c. The unfolding transition is presented as a plot of ellipticity at 220 nm in millidegrees

Guanidine HCl-induced unfolding of wild-type iso-1-cytochrome c. The unfolding transition is presented as a plot of ellipticity at 22 nm in millidegrees

Guanidine hydrochloride ,

Guanidine hydrochloride dena-turation of lysozyme. Curves are drawn according to the equation AG AGq .

Guanidine hydrochloride-induced denaturation of carbonic anhydrase B. The transition was followed by various methods .

Guanidine hydrochloride-induced transition of elastase measured by circular dichroism .

Guanidine mediated esterification and alcoholysis

Guanidine structure.

Guanidine-base-catalyzed aldol reaction of 5H-oxazol-4-ones.



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