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Published in 2017 at "Journal of Saudi Chemical Society"
DOI: 10.1016/j.jscs.2016.01.003
Abstract: MgO nanoparticles have been used as an efficient catalyst for the diastereoselective preparation of trans-2-benzoyl-3-(aryl)-2H-furo[3,2-c]chromen-4(3H)-ones by the multi-component reaction of 2,4′-dibromoacetophenone, pyridine, benzaldehydes and 4-hydroxycoumarin under ultrasonic irradiation. This interesting result revealed that the pyridiniumylide…
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Keywords:
diastereoselective synthesis;
synthesis trans;
ultrasonic irradiation;
mgo nanoparticles ... See more keywords
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Published in 2021 at "Tetrahedron"
DOI: 10.1016/j.tet.2021.132257
Abstract: Abstract The N-sulfonyl spiroaziridine oxindole is a recently developed versetile precusor in synthesis of wide range of 3,3-disubstitued/spirooxindoles. It usually prepared in three steps from isatin and needs costly and limited available sulfinimides and hazardous…
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Keywords:
trans amino;
synthesis;
synthesis trans;
aminoarylation synthesis ... See more keywords
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Published in 2017 at "Tetrahedron Letters"
DOI: 10.1016/j.tetlet.2016.12.002
Abstract: Abstract An efficient and simple method is described for the synthesis of trans-4,5-diaminocyclopent-2-enones via reaction of furfural and secondary amines, using ErCl3·6H2O immobilized on silica allowing an efficient catalyst reuse using n-butanol/n-hexane as the reaction…
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Keywords:
trans diaminocyclopent;
diaminocyclopent enones;
synthesis trans;
enones furfural ... See more keywords
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Published in 2022 at "Organic letters"
DOI: 10.1021/acs.orglett.2c02509
Abstract: An efficient visible-light-induced synthesis of trans-oxiranes has been accomplished via decarboxylative stereospecific epoxidation of trans-cinnamic acids by aryldiazonium salts using CuCl, eosin Y, TBHP, and DBU. The reaction is facile, straightforward, and endowed with good…
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Keywords:
trans oxiranes;
stereospecific epoxidation;
via decarboxylative;
visible light ... See more keywords
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Published in 2023 at "Organic letters"
DOI: 10.1021/acs.orglett.3c01040
Abstract: A silver-mediated homocoupling of N-triftosylhydrazones for the construction of trans-stilbenes has been presented. This protocol is characterized by its suitability for both inter- and intramolecular reactions, operational simplicity, high efficiency with excellent stereoselectivity, broad substrate…
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Keywords:
stilbenes silver;
catalyzed self;
trans stilbenes;
stereoselective synthesis ... See more keywords
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Published in 2020 at "Organic chemistry frontiers"
DOI: 10.1039/c9qo01489f
Abstract: Aziridines are ubiquitous in bioactive molecules and often serve as key synthetic building blocks. We report herein an intramolecular KI/TBHP mediated oxidative dehydrogenative C(sp3)–H amination reaction to synthesize a diverse array of trans-2,3-disubstituted aziridines in…
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Keywords:
synthesis trans;
stereoselective synthesis;
sp3;
sp3 amination ... See more keywords
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Published in 2017 at "Journal of Chemical Research"
DOI: 10.3184/174751917x14967701767058
Abstract: We report a green and efficient method for the synthesis of trans-[3-(aryl)-2,3-dihydrofuro[3,2-h]quinolin-2-yl]-(4-chlorophenyl) methanones from the condensation of 2-[2-(4-chlorophenyl)-2-oxoethyl)]isoquinolinium bromide with 8-hydroxyquinoline and an aromatic aldehyde in the presence of catalytic amounts of choline hydroxide in…
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Keywords:
quinolin chlorophenyl;
chlorophenyl;
trans aryl;
synthesis trans ... See more keywords