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...cle.asp?doi=JR9620000470 Abstract]</ref><ref>''Studies on the oxidation of hydrazones with iodine and with phenylselenenyl bromide in the presence of strong orga ...r roots with the 1911 discovery by Wieland and Roseeu that the reaction of hydrazones with iodine alone (without base) results in the [[azine]] dimer (structure ...

{{Short description|Organic compounds - Hydrazones}} '''Hydrazones''' are a class of [[organic compound]]s with the structure {{chem2|R^{1}R^{ ...

...hors=Gleason CH, Parker JM|title=The duration of activity of the benziloyl hydrazones of testosterone-17-heptanoate, estrone-3-heptanoate and 17α-hydroxy-proges [[Category:Hydrazones]] ...

...</sub>-catalyzed synthesis of azines and 3,5-diphenyl-1''H''-pyrazole from hydrazones and/or ketones monitored by high resolution ESI⁺-MS|year = 2018| ...t4=M. C.|title=The preparation of secondary aliphatic diazo-compounds from hydrazones|journal=Journal of the Chemical Society C: Organic|date=1966|pages=467|doi= ...

...[[tautomer]]ic forms: hydrazide imides (RC(=NH)NHNH₂) and amide hydrazones (RC(NH₂)=NNH₂).<ref>{{cite book | chapter = Amidrazon ...

...d to generate toluenesulfonyl hydrazones. When derived from ketones, these hydrazones participate in the [[Shapiro reaction]]<ref>{{cite journal|last = Shapiro|f ...

[[Category:Hydrazones]] ...

...variations at the imine functionality of 4-bromophenylacetic acid derived hydrazones on alkaline phosphatase inhibition: synthesis and molecular modelling studi ...double bond with the second nitrogen.<ref name=khan/> At least 19 of these hydrazones are known.<ref name=khan/> ...

[[Category:Hydrazones]] ...

=== From hydrazones === ...

...дразин]]а<ref>{{Cite web |url=http://goldbook.iupac.org/H02884.html |title=hydrazones // IUPAC Gold Book |access-date=2011-02-09 |archive-date=2012-10-20 |archiv ...ных ненуклеофильных оснований образуют винилйодиды<ref>''A new reaction of hydrazones'' Barton, D. H. R., R. E. O'Brien and S. Sternhell Journal of the Chemical ...

[[Category:Hydrazones]] ...

...carbonyl compounds and the chiral enamine species reported previously, the hydrazones exhibit higher reactivity, [[regioselectivity]] and [[stereoselectivity]].< ...ly attacks [[electrophiles]], such as alkyl halides, to generate alkylated hydrazones with simultaneous creation of a new [[chiral]] center at the α-carbon. ...

...AMP chiral hydrazones using SAMP or RAMP as a chiral auxiliary. The chiral hydrazones are then [[metalation|metalated]] with [[lithium diisopropylamide]] (LDA) a ...

[[Category:Hydrazones]] ...

...hydroquinone to p-benzoquinone, benzylamine to benzaldehyde, [[Hydrazone|hydrazones]] to [[Diazo compound|diazo compounds]], ...

...scher indole synthesis can be effected by cross-coupling aryl bromides and hydrazones.<ref>{{Cite journal | last1 = Wagaw| first1 = S. | last2 = Yang|first2 = B. ...

[[Category:Hydrazones]] ...

...country = US | number = 3972878 | title = Method for preparing azines and hydrazones | issue-date = 1976-08-03}}.{{cite patent | inventor1-first = Jean-Pierre | ...