Results 11 to 20 of about 2,558 (239)

Intramolecular Buchwald-Hartwig N-Arylation of Bicyclic Hydrazines: Practical Access to Spiro[indoline-2,3\u27-piperidines]

open access: yes, 2022
In recent years, spirocycles have been the focus of medicinal chemistry, and several drugs or drug candidates incorporating these “non-planar” chemical motifs have been developed.
Yann, Foricher   +4 more
core   +1 more source

Reductive Hydrazination with Trichlorosilane: A Method for the Preparation of 1,1-Disubstituted Hydrazines

open access: yes, 2016
A straightforward and facile method has been developed to prepare 1,1-disubstituted hydrazines via Lewis base promoted direct reductive hydrazination. Under the catalysis of hexamethylphosphoramide (HMPA) and N,N-dimethylacetamide (DMAc), respectively ...
Di, X   +5 more
core   +2 more sources

2-tert-Butyl-5,6,7,8,9,10-hexahydrocyclohepta[b]indole

open access: yesMolbank, 2011
2-tert-Butyl-5,6,7,8,9,10-hexahydrocyclohepta[b]indole was synthesized by reaction of cycloheptanone and (4-tert-butylphenyl)hydrazine hydrochloride in the presence of sodium acetate and sulfuric acid in glacial acetic acid via Fischer indole synthesis.
Janina Wobbe   +5 more
doaj   +1 more source

Synthesis of the Fmoc-aza-Arg(Boc)2 precursor via hydrazine alkylation; pp. 438–443 [PDF]

open access: yesProceedings of the Estonian Academy of Sciences, 2014
The aza-arginine precursor Fmoc-aza-Arg(Boc)2 was synthesized starting from mono-protected hydrazines via an aza-ornithine precursor. This reaction path is shorter and more efficient than the reductive alkylation reaction.
Anton Mastitski   +2 more
doaj   +1 more source

Synthesis of N-CF3 hydrazines through radical trifluoromethylation of azodicarboxylates

open access: yes, 2021
International audienceNovel family of N -CF 3 hydrazines have been prepared from a direct way involving the available and cheap Langlois ...
Crousse, Benoît   +3 more
core   +1 more source

Ultrasonics Promoted Synthesis of 5-(Pyrazol-4-yl)-4,5-Dihydropyrazoles Derivatives

open access: yesApplied Sciences, 2013
A series of new 1,3-diaryl-5-(1-phenyl-3-methyl-5-chloropyrazol-4-yl)-4,5-dihydropyrazole derivatives have been synthesized under sonication conditions in ethanol or methanol/glacial acetic acid mixture (5/1 ratio) with two equivalents of hydrazines and ...
Manuel Nogueras   +4 more
doaj   +1 more source

Conception et synthèse de nouvelles hydrazines fluorées

open access: yes, 2022
Thanks to particular Physico-chemical properties, fluorine is becoming increasingly important in medicinal chemistry. Hydrazines are essential for synthesising N-heterocyclic functionalised compounds and for their many applications in many areas of ...
Cao, Tingting
core   +1 more source

Rhodium-Catalyzed Addition–Cyclization of Hydrazines with Alkynes: Pyrazole Synthesis via Unexpected C–N Bond Cleavage

open access: yes, 2016
Rhodium-catalyzed addition–cyclization of hydrazines with alkynes has been achieved to afford highly substituted pyrazoles under mild conditions. The cascade reaction involves two transformations: addition of the C–N bond of hydrazines to alkynes via ...
Xiao Feng Mao (1784368)   +4 more
core   +3 more sources

Synthesis of certain nitropyridine derivatives bearing 2-thiazolyl hydrazines with expected monoamine oxidase inhibitory activity [PDF]

open access: yesBulletin of Pharmaceutical Sciences. Assiut University, 1999
Two series of nitropyridine derivs. bearing 2-​thiazolyl hydrazines were synthesized and evaluated for their monoamine oxidase (MAO) inhibitory activity by in vitro tests to assay their effect on rat liver mitochondria by a kynuramine fluorimetric assay.
Hoda Hassan
doaj   +1 more source

Electrophilically Activated Nitroalkanes in Double Annulation of [1,2,4]Triazolo[4,3-a]quinolines and 1,3,4-Oxadiazole Rings

open access: yesMolecules, 2021
Nitroalkanes activated with polyphosphoric acid could serve as efficient electrophiles in reactions with amines and hydrazines, enabling various cascade transformations toward heterocyclic systems.
Alexander V. Aksenov   +6 more
doaj   +1 more source

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