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Published in 2017 at "Journal of Heterocyclic Chemistry"
DOI: 10.1002/jhet.2684
Abstract: The 1,3-dipolar cycloaddition reaction of (E,E)-1,3-bis(arylidene)indan-2-one with diarylnitrilimines, generated in situ via dehydrohalogenation of the corresponding hydrazonoyl chlorides , affords predominantly monospiropyrazolines and as a mixture of diastereoisomers. Also dispiropyrazolines are formed in moderate yields.…
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Keywords:
cycloaddition;
mono dispiropyrazoline;
synthesis mono;
dispiropyrazoline derivatives ... See more keywords
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Published in 2019 at "Chemistry of Heterocyclic Compounds"
DOI: 10.1007/5109
Abstract: An effective method was developed for the synthesis of 1,3,5-trisubstituted pyrazoles by using acetylenic ketones, obtained from ethyl 5-ethynylanthranilate, in reactions with substituted hydrazines and hydrazides. It was shown that the cyclization of ethyl 5-(3-aryl-3-oxopropinyl)anthranilates…
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Keywords:
containing anthranilic;
pyrazoles containing;
trisubstituted pyrazoles;
synthesis trisubstituted ... See more keywords
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Published in 2020 at "Russian Chemical Bulletin"
DOI: 10.1007/s11172-020-2724-8
Abstract: The gas-phase copyrolysis of chlorotrifluoroethylene with buta-1,3-diene, penta-1,3-diene, or isoprene in a flow reactor at 440–480°C gave 4-chloro-4,5,5-trifluorocyclohex-1-enes. The latter treated with aqueous KOH under condition of phase-transfer catalysis were selectively converted into 1,2-difluorobenzene, 2,3-difluorotoluene,…
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Keywords:
chlorotrifluoroethylene buta;
step regioselective;
synthesis difluorobenzenes;
difluorobenzenes chlorotrifluoroethylene ... See more keywords
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Published in 2019 at "Chemical Papers"
DOI: 10.1007/s11696-019-00790-1
Abstract: Synthesis of (E)-2-hydroxy-5-(aryldiazenyl)benzaldehydes was investigated. Various Lewis acids were tested as catalyst to achieve regioselectivity. In addition to various commercial catalysts, mesoporous Zn/SBA-15 was synthesized through a modified direct method with chloride salt as zinc…
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Keywords:
aryl azo;
synthesis;
azo salicylaldehydes;
regioselective synthesis ... See more keywords
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Published in 2018 at "Journal of Fluorine Chemistry"
DOI: 10.1016/j.jfluchem.2018.07.013
Abstract: Abstract Efficient regioselective synthesis of 3-CF3-substituted thiophene derivatives was elaborated using addition of methyl thioglycolate to CF3-ynones in the presence of sodium methoxide.
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Keywords:
cf3 ynones;
cf3;
synthesis cf3;
thiophene derivatives ... See more keywords
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Published in 2018 at "Mendeleev Communications"
DOI: 10.1016/j.mencom.2018.11.020
Abstract: The effective and regioselective synthesis of new (2-hydrazinylthiazol-4-yl)furoxan hydrobromides based on the condensation of (bromoacetyl)furoxans with thiosemicarbazide has been developed. The cytotoxic activity of their derivatives (with hydrazone, 4-thiazolo[2.3-c][1,2,4]triazole or pyrrole moieties) against two human…
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Keywords:
cytotoxic;
synthesis structural;
structural diversification;
regioselective synthesis ... See more keywords
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Published in 2018 at "Tetrahedron"
DOI: 10.1016/j.tet.2018.09.043
Abstract: Abstract Two regioselective synthetic routes towards 3,5-disubstituted isoxazoles from ynones are reported. One route takes place via first converting the ynones to ynone O-methyl oximes, followed by a palladium-catalyzed intramolecular cyclization. The other involves the…
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Keywords:
disubstituted isoxazoles;
complementary regioselective;
isoxazoles ynones;
synthesis disubstituted ... See more keywords
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Published in 2019 at "Tetrahedron"
DOI: 10.1016/j.tet.2019.130695
Abstract: Abstract An efficient synthesis of 1,2,3,4-tetrahydroquinolines with donor and acceptor group has been delineated by base mediated ring transformation of 6-aryl-4-substituted-2H-pyran-2-one-3-carbonitriles by N-boc-3-piperidone followed by consecutive deprotection of Boc group under acidic conditions. This reaction…
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Keywords:
promoted regioselective;
boc piperidone;
base promoted;
regioselective synthesis ... See more keywords
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Published in 2021 at "Tetrahedron"
DOI: 10.1016/j.tet.2021.132214
Abstract: Abstract An interesting and facile triflic acid catalysed annulation of α-aryl carbonyls with arylalkynes is presented for the regioselective synthesis of substituted naphthalenes. The annulation reaction involves a sequence of electrophilic attack of carbonyl on…
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Keywords:
triflic acid;
synthesis substituted;
carbonyls;
acid catalysed ... See more keywords
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Published in 2020 at "Journal of Chemical Education"
DOI: 10.1021/acs.jchemed.0c00039
Abstract: Keto–enol tautomerism is a special example of structural isomerism. In this experiment, 6-chlorofulvene is predominantly yielded during the chlorination reaction of 6′-hydroxyfulvene with POCl3 in ...
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Keywords:
keto enol;
regioselective synthesis;
chlorofulvene;
enol tautomerism ... See more keywords
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Published in 2021 at "Organic letters"
DOI: 10.1021/acs.orglett.1c01398
Abstract: We describe, for the first time, a highly regioselective hydrosilylation of propargylic amines. The reaction utilizes a PtCl2/XantPhos catalyst system to deliver hydrosilanes across the alkyne to afford multifunctional allylic amines in high yields. The…
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Keywords:
multifunctional allylic;
amines access;
allylic amines;
synthesis multifunctional ... See more keywords