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Aldehydes sulfonyl hydrazides

Fig. 1.47. Myers synthesis of atkanes from aldehydes via the sulfonylated hydrazones B and their silyl derivatives C. This procedure provides a skeletongenerating three-step synthesis of alkanes from aldehydes. In terms of Figure 1.2, the chain reaction F —> I involved is a "substitution reaction by fragmentation." (The sulfonylated hydrazide anion, which here results from the addition of R3-Li to the sulfonyl hydrazone C, does—at this reaction s temperature of-78 °C—not release toluene sulfinate. Compare the different behavior of the sulfonylated hydrazide anion C in the reaction of Figure 17.69, where a mesitylene sulfinate residue is eliminated at a temperature that is higher by 160 °C). Fig. 1.47. Myers synthesis of atkanes from aldehydes via the sulfonylated hydrazones B and their silyl derivatives C. This procedure provides a skeletongenerating three-step synthesis of alkanes from aldehydes. In terms of Figure 1.2, the chain reaction F —> I involved is a "substitution reaction by fragmentation." (The sulfonylated hydrazide anion, which here results from the addition of R3-Li to the sulfonyl hydrazone C, does—at this reaction s temperature of-78 °C—not release toluene sulfinate. Compare the different behavior of the sulfonylated hydrazide anion C in the reaction of Figure 17.69, where a mesitylene sulfinate residue is eliminated at a temperature that is higher by 160 °C).
Aldehydes, reducing sugars, ketones Dansyl hydrazide-1-dimethyl aminonaphthalene-5-sulfonyl hydrazide... [Pg.203]

Lissamine rhodamine B sulfonyl hydrazine is a hydrazide derivative of sulforhodamine B that can spontaneously react with aldehyde- or ketone-containing molecules to form a covalent,... [Pg.427]

Lissamine rhodamine B sulfonyl hydrazine is a hydrazide derivative of sulforhodamine B that can spontaneously react with aldehyde- or ketone-containing molecules to form a covalent, hydrazone linkage (Fig. 217). It also can be used to label cytosine residues in DNA or RNA by use of the bisulfite activation procedure (Chapter 17, Section 2.1). The resulting fluorescent derivative exhibits an excitation maximum at a wavelength of 556 nm and a maximal emission wavelength of 580 nm when dissolved in methanol. In... [Pg.348]

The hydrazide derivative can be used to modify aldehyde- or ketone-containing molecules, including cytosine residues using the bisulfite activation procedure described in Chapter 17, Section 2.1. The sulfonyl hydrazine group of Texas Red hydrazide reacts with aldehydes or ketones in target functional groups to form hy-drazone bonds (Fig. 218). Carbohydrates and glycoconjugates can be specifically labeled at the polysaccharide portion if the required aldehydes are first formed by periodate oxidation or another such method (Chapter 1, Section 4.4). [Pg.350]


See other pages where Aldehydes sulfonyl hydrazides is mentioned: [Pg.470]    [Pg.7921]    [Pg.427]    [Pg.429]    [Pg.439]    [Pg.708]   
See also in sourсe #XX -- [ Pg.172 , Pg.200 ]




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Aldehydes hydrazides

Hydrazide aldehydes

Sulfonyl hydrazide

Sulfonyl hydrazides

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