Results 81 to 90 of about 2,558 (239)

Kinetic Spectrophotometric Determination of Propellant Grade Hydrazines using Thiophenes with Active Carbonyl Groups

open access: yes, 2014
A simple, cost effective, highly sensitive and rapid kinetic spectrophotometric method was developed for hydrazines by using Thiophene-3-carboxaldehyde (3-Thienaldehyde) and 3-Butenone (E)-1,1,1-trifluoro-4-(3-thienyl) (CF3 enone). CF3 enone was prepared
Subramanian, Selvakumar   +2 more
core   +1 more source

Toxicological profile for hydrazines [PDF]

open access: yes
prepared by Sciences International, Inc. under subcontract to Research Triangle Institute.205-93-0606Includes bibliographical references (p. 155-182)

core  

Oxidative Heck Reaction of Glycals and Aryl Hydrazines: A Palladium-Catalyzed C‑Glycosylation

open access: yes, 2016
An efficient Heck-type C-glycosylation of glycals via the C–N bond cleavage of aryl hydrazines has been developed. The flexibility of the reaction was tested by the substrate scope, consisting of glycals from different carbohydrate origins as well as ...
Le Mai Hoang Kim (1915654)   +3 more
core   +1 more source

Late‐Stage Functionalization of Peptides on the Solid Phase

open access: yesAngewandte Chemie International Edition, EarlyView.
Peptide modifications are essential to control pharmacodynamic and pharmacokinetic properties of peptide drugs. Consequently, strategies that allow for efficient and rapid incorporation of non‐canonical modifications into peptides in parallel formats are highly sought after.
Marius Werner   +2 more
wiley   +1 more source

Synthetic methodology for alkyl substituted hydrazines

open access: yes, 2001
Substituted hydrazines have found many technical and commercial applications and this is reflected in the immense number of such compounds synthesized to date.
Ragnarsson, U,
core  

Trifluoroacetyl-Activated Nitrogen−Nitrogen Bond Cleavage of Hydrazines by Samarium(II) Iodide

open access: yes, 2016
Trifluoroacetyl derivatives of hydrazines undergo clean and efficient reductive cleavage of the N−N bond with SmI2 in the presence of MeOH. After N-trifluoroacetylation, acyl-, aryl-, and alkyl-substituted hydrazines are reductively cleaved by this ...
Hui Ding (308976)   +1 more
core   +1 more source

Formation of Metallacyclobutene Complexes via the Addition of Hydrazines to Ruthenium Vinylidene Complexes

open access: yes, 2016
The reaction between monosubstituted hydrazines and Ru(II) vinylidene complexes [RuCl(P∩N)2(CCH(R))]BPh4 (where R = Ph, n-Bu and P∩N = 3,5-dimethyl[1-((2-diphenylphosphino)ethyl)]pyrazole (Me2PyP)) afforded metallacyclobutene derivatives of the general
Jörg Wagler (1565395)   +2 more
core   +3 more sources

On the reactivity of triphenylphosphoranylidenesuccinic anhydride with nitrogen nucleophiles: a new synthetic route to nitrogen-containing phosphonium salts

open access: yesJournal of the Brazilian Chemical Society, 2000
The reactions of triphenylphosphoranylidenesuccinic anhydride with amines, hydrazines and dipolar nitrogen nucleophiles were investigated, and a new method of synthesis of phosphonioum salts containing the fragment RNHC(C=O)CH2CH2PPh3 is described.
Cunha Silvio, Kascheres Albert
doaj  

FLUOROUS SUPPORTED SYNTHESIS OF PYRAZOLONE DERIVATIVES FROM ALLYLIC ALCOHOLS USING A PALLADIUM-CATALYZED STRATEGY

open access: yesQuímica Nova
Ten substituted pyrazolone derivatives were easily synthesized from perfluorinated allylic alcohols, via a straightforward two steps reaction involving a Heck-coupling/isomerization reaction and subsequent condensation of hydrazines.
Nicolas Gouault   +4 more
doaj   +1 more source

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