Synthesis of 1,2,3,4-tetrahydroisoquinolines by microreactor-mediated thermal isomerization of laterally lithiated arylaziridines.
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Contribution of microreactor technology and flow chemistry to the development of green and sustainable synthesisContinuous flow magnesiation of functionalized heterocycles and acrylates with TMPMgCl⋅LiCl.LiAlH4 -Induced Selective Ring Rearrangement of 2-(2-Cyanoethyl)aziridines toward 2-(Aminomethyl)pyrrolidines and 3-Aminopiperidines as Eligible Heterocyclic Building Blocks.A convenient enantioselective CBS-reduction of arylketones in flow-microreactor systems.A direct and sustainable synthesis of tertiary butyl esters enabled by flow microreactors.Synthesis in mesoreactors: Ru(porphyrin)CO-catalyzed aziridination of olefins under continuous flow conditions
P2860
Synthesis of 1,2,3,4-tetrahydroisoquinolines by microreactor-mediated thermal isomerization of laterally lithiated arylaziridines.
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2013 nî lūn-bûn
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2013年の論文
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2013年学术文章
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name
Synthesis of 1,2,3,4-tetrahydr ...... ally lithiated arylaziridines.
@en
Synthesis of 1,2,3,4-tetrahydr ...... ally lithiated arylaziridines.
@nl
type
label
Synthesis of 1,2,3,4-tetrahydr ...... ally lithiated arylaziridines.
@en
Synthesis of 1,2,3,4-tetrahydr ...... ally lithiated arylaziridines.
@nl
prefLabel
Synthesis of 1,2,3,4-tetrahydr ...... ally lithiated arylaziridines.
@en
Synthesis of 1,2,3,4-tetrahydr ...... ally lithiated arylaziridines.
@nl
P2093
P2860
P356
P1476
Synthesis of 1,2,3,4-tetrahydr ...... ally lithiated arylaziridines.
@en
P2093
Aiichiro Nagaki
Arianna Giovine
Aurelia Falcicchio
Biagia Musio
Jun-ichi Yoshida
P2860
P304
P356
10.1002/CHEM.201203533
P407
P577
2013-01-15T00:00:00Z