Selective monoalkylation of amines with light electrophiles using a flow microreactor system

Literature Information

Publication Date 2015-02-03
DOI 10.1039/C4QO00342J
Impact Factor 5.281
Authors

Thomas Lebleu, Jacques Maddaluno, Julien Legros


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Abstract

The challenging direct monoalkylation of amines with light electrophilic reagents (C1 to C3) was performed through a flow microreactor approach. The efficiency of mixing coupled with short residence times (tR = 0.7–62 s) allows the transfer of a single alkyl group from R-OTf onto primary amines (R = Et, Pr) as well as on secondary amines (R = Me, Et, Pr, allyl, propargyl) with good selectivities.

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Front/Back Matter

DOI: 10.1039/B805757P

Back cover

Front/Back Matter

DOI: 10.1039/B802345J

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Organic Chemistry Frontiers

Organic Chemistry Frontiers
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Organic Chemistry Frontiers publishes high-quality research from across organic chemistry. Emphases are placed on studies that make significant contributions to the field of organic chemistry by reporting either new or significantly improved protocols or methodologies. Topics include, but are not limited to the following: Organic synthesis Development of synthetic methodologies Catalysis Natural products Functional organic materials Supramolecular and macromolecular chemistry Physical and computational organic chemistry

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