Hidrazonok (Hungarian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hidrazonok" in Hungarian language version.

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9doi.org

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4orgsyn.org

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4nih.gov

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2archive.org

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1archives-ouvertes.fr

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1niscair.res.in

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archive.org

(2005. szeptember 7.) „Arming antibodies: prospects and challenges for immunoconjugates”. Nature Biotechnology 23 (9), 1137–46. o. DOI:10.1038/nbt1141. PMID 16151407.
(2010) „N,N-dialkylhydrazones in organic synthesis. From simple N,N-dimethylhydrazones to supported chiral auxiliaries”. Chemical Reviews 110 (3), 1386–1434. o. DOI:10.1021/cr900067y. PMID 20000672.

archives-ouvertes.fr

hal.archives-ouvertes.fr

(2014) „Solvent-free mechanochemical route for green synthesis of pharmaceutically attractive phenol-hydrazones”. RSC Adv. 4 (100), 56736–56742. o. DOI:10.1039/c4ra10489g.

doi.org

dx.doi.org

(2005. szeptember 7.) „Arming antibodies: prospects and challenges for immunoconjugates”. Nature Biotechnology 23 (9), 1137–46. o. DOI:10.1038/nbt1141. PMID 16151407.
(2008) „Hydrolytic stability of hydrazones and oximes”. Angew. Chem. Int. Ed. 47 (39), 7523–6. o. DOI:10.1002/anie.200802651. PMID 18712739. PMC 2743602.
(2014) „Solvent-free mechanochemical route for green synthesis of pharmaceutically attractive phenol-hydrazones”. RSC Adv. 4 (100), 56736–56742. o. DOI:10.1039/c4ra10489g.
(2008) „New one step synthesis of 3,5-disubstituted pyrazoles under microwave irradiation and classical heating”. Journal of Heterocyclic Chemistry 45 (2), 503–505. o. DOI:10.1002/jhet.5570450231.
(2014) „One-pot synthesis of 3,5-diphenyl-1H-pyrazoles from chalcones and hydrazine under mechanochemical ball milling”. Heterocycles 89 (1), 103–112. o. DOI:10.3987/COM-13-12867.
(2010) „N,N-dialkylhydrazones in organic synthesis. From simple N,N-dimethylhydrazones to supported chiral auxiliaries”. Chemical Reviews 110 (3), 1386–1434. o. DOI:10.1021/cr900067y. PMID 20000672.
(1976) „Applications of N,N-dimethylhydrazones to synthesis. Use in efficient, positionally and stereochemically selective C_C bond formation; oxidative hydrolysis to carbonyl compounds”. Tetrahedron Letters 17 (1), 3. o. DOI:10.1016/S0040-4039(00)71307-4.
(1978) „Herstellung und synthetische Verwendung von metallierten Dimethylhydrazonen Regio- und stereoselektive Alkylierung von Carbonylverbindungen”. Chemische Berichte 111 (4), 1337–1361. o. DOI:10.1002/cber.19781110413.
(1977) „Enantioselective alkylation of aldehydes via metalated chiral hydrazones”. Tetrahedron Letters 18 (23), 191–194. o. DOI:10.1016/S0040-4039(01)92585-7.

nih.gov

pubmed.ncbi.nlm.nih.gov

(2005. szeptember 7.) „Arming antibodies: prospects and challenges for immunoconjugates”. Nature Biotechnology 23 (9), 1137–46. o. DOI:10.1038/nbt1141. PMID 16151407.
(2008) „Hydrolytic stability of hydrazones and oximes”. Angew. Chem. Int. Ed. 47 (39), 7523–6. o. DOI:10.1002/anie.200802651. PMID 18712739. PMC 2743602.
(2010) „N,N-dialkylhydrazones in organic synthesis. From simple N,N-dimethylhydrazones to supported chiral auxiliaries”. Chemical Reviews 110 (3), 1386–1434. o. DOI:10.1021/cr900067y. PMID 20000672.

ncbi.nlm.nih.gov

(2008) „Hydrolytic stability of hydrazones and oximes”. Angew. Chem. Int. Ed. 47 (39), 7523–6. o. DOI:10.1002/anie.200802651. PMID 18712739. PMC 2743602.

niscair.res.in

nopr.niscair.res.in

Lasri, Jamal (2018). „Metal-free and FeCl₃-catalyzed synthesis of azines and 3,5-diphenyl-1H-pyrazole from hydrazones and/or ketones monitored by high resolution ESI⁺-MS”. Indian Journal of Chemistry, Section B 57B (3), 362–373. o.

orgsyn.org

(1977) „Monoalkylation of α,β-Unsaturated Ketones via Metalloenamines: 1-butyl-10-methyl-Δ¹⁽⁹⁾-2-octalone”. Org. Synth. 57, 69. o. ; Coll. Vol. 6: 242
(1970) „Acetone hydrazone”. Org. Synth. 50, 3. o. ; Coll. Vol. 6: 10
(1987) „(S)-(−)-1-Amino-2-methoxymethylpyrrolidine (SAMP) and (R)-(+)-1-amino-2-methoxymethylpyrrolidine (RAMP), versatile chiral auxiliaries”. Org. Synth. 65, 173. o. ; Coll. Vol. 8: 26
(1987) „Asymmetric syntheses using the SAMP-/RAMP-hydrazone method: (S)-(+)-4-methyl-3-heptanone”. Org. Synth. 65, 183. o. ; Coll. Vol. 8: 403