Synthesis of amines with pendant boronic esters by borrowing hydrogen catalysis

Winson M. J. Ma; Tony D. James; Jonathan M. J. Williams

doi:10.1021/ol402271a

Synthesis of amines with pendant boronic esters by borrowing hydrogen catalysis

Winson M. J. Ma, Tony D. James, Jonathan M. J. Williams

Research output: Contribution to journal › Article › peer-review

30 Citations (SciVal)

Abstract

Amine alkylation reactions of alcohols have been performed in the presence of boronic ester groups to provide products which are known to have use as molecular sensors. The boronic ester moiety could be present in either the alcohol or amine starting material and was not compromised in the presence of a ruthenium catalyst.

Original language	English
Pages (from-to)	4850-4853
Number of pages	4
Journal	Organic Letters
Volume	15
Issue number	18
Early online date	9 Sept 2013
DOIs	https://doi.org/10.1021/ol402271a
Publication status	Published - 20 Sept 2013

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10.1021/ol402271a

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title = "Synthesis of amines with pendant boronic esters by borrowing hydrogen catalysis",

abstract = "Amine alkylation reactions of alcohols have been performed in the presence of boronic ester groups to provide products which are known to have use as molecular sensors. The boronic ester moiety could be present in either the alcohol or amine starting material and was not compromised in the presence of a ruthenium catalyst.",

author = "Ma, {Winson M. J.} and James, {Tony D.} and Williams, {Jonathan M. J.}",

year = "2013",

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doi = "10.1021/ol402271a",

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journal = "Organic Letters",

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AU - Ma, Winson M. J.

AU - James, Tony D.

AU - Williams, Jonathan M. J.

PY - 2013/9/20

Y1 - 2013/9/20

N2 - Amine alkylation reactions of alcohols have been performed in the presence of boronic ester groups to provide products which are known to have use as molecular sensors. The boronic ester moiety could be present in either the alcohol or amine starting material and was not compromised in the presence of a ruthenium catalyst.

AB - Amine alkylation reactions of alcohols have been performed in the presence of boronic ester groups to provide products which are known to have use as molecular sensors. The boronic ester moiety could be present in either the alcohol or amine starting material and was not compromised in the presence of a ruthenium catalyst.

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UR - http://dx.doi.org/10.1021/ol402271a

U2 - 10.1021/ol402271a

DO - 10.1021/ol402271a

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VL - 15

SP - 4850

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JO - Organic Letters

JF - Organic Letters

IS - 18

ER -

Synthesis of amines with pendant boronic esters by borrowing hydrogen catalysis

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Synthesis of amines with pendant boronic esters by borrowing hydrogen catalysis

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