Novel quaternary ammoniumboronate salts as selective acylation catalysts

Venkata Jaganmohan Reddy; Joanne Muriithi; Venkatram R Mereddy

doi:10.1016/j.molcata.2007.02.019

Novel quaternary ammoniumboronate salts as selective acylation catalysts

Venkata Jaganmohan Reddy, Joanne Muriithi, Venkatram R Mereddy

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

1 Scopus citations

Abstract

N-boronomethyltrialkylammonium salts were prepared via the reaction of trialkyl amines with α-halomethylboronates. These compounds were utilized as selective catalysts for acetylation of primary alcohols and aldehydes.

Original language	English (US)
Pages (from-to)	86-88
Number of pages	3
Journal	Journal of Molecular Catalysis A: Chemical
Volume	271
Issue number	1-2
DOIs	https://doi.org/10.1016/j.molcata.2007.02.019
State	Published - Jun 18 2007
Externally published	Yes

Bibliographical note

Funding Information:
This research was supported by grants from Research Corporation (CC6961), American Cancer Society (IRG-58-001-46-IRG51), and the Grant-in-Aid (20206) administered by the University of Minnesota. We also thank the Aldrich Chemical Company for the financial support.

Copyright:
Copyright 2008 Elsevier B.V., All rights reserved.

Keywords

Acetylation
Acylal
Boronomethylammonium salts
Iodomethylpinacolboronate

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10.1016/j.molcata.2007.02.019

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title = "Novel quaternary ammoniumboronate salts as selective acylation catalysts",

abstract = "N-boronomethyltrialkylammonium salts were prepared via the reaction of trialkyl amines with α-halomethylboronates. These compounds were utilized as selective catalysts for acetylation of primary alcohols and aldehydes.",

keywords = "Acetylation, Acylal, Boronomethylammonium salts, Iodomethylpinacolboronate",

author = "Reddy, {Venkata Jaganmohan} and Joanne Muriithi and Mereddy, {Venkatram R}",

note = "Funding Information: This research was supported by grants from Research Corporation (CC6961), American Cancer Society (IRG-58-001-46-IRG51), and the Grant-in-Aid (20206) administered by the University of Minnesota. We also thank the Aldrich Chemical Company for the financial support. Copyright: Copyright 2008 Elsevier B.V., All rights reserved.",

year = "2007",

month = jun,

day = "18",

doi = "10.1016/j.molcata.2007.02.019",

language = "English (US)",

volume = "271",

pages = "86--88",

journal = "Journal of Molecular Catalysis A: Chemical",

issn = "1381-1169",

publisher = "Elsevier B.V.",

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TY - JOUR

T1 - Novel quaternary ammoniumboronate salts as selective acylation catalysts

AU - Reddy, Venkata Jaganmohan

AU - Muriithi, Joanne

AU - Mereddy, Venkatram R

N1 - Funding Information: This research was supported by grants from Research Corporation (CC6961), American Cancer Society (IRG-58-001-46-IRG51), and the Grant-in-Aid (20206) administered by the University of Minnesota. We also thank the Aldrich Chemical Company for the financial support. Copyright: Copyright 2008 Elsevier B.V., All rights reserved.

PY - 2007/6/18

Y1 - 2007/6/18

N2 - N-boronomethyltrialkylammonium salts were prepared via the reaction of trialkyl amines with α-halomethylboronates. These compounds were utilized as selective catalysts for acetylation of primary alcohols and aldehydes.

AB - N-boronomethyltrialkylammonium salts were prepared via the reaction of trialkyl amines with α-halomethylboronates. These compounds were utilized as selective catalysts for acetylation of primary alcohols and aldehydes.

KW - Acetylation

KW - Acylal

KW - Boronomethylammonium salts

KW - Iodomethylpinacolboronate

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U2 - 10.1016/j.molcata.2007.02.019

DO - 10.1016/j.molcata.2007.02.019

M3 - Article

AN - SCOPUS:34248219045

SN - 1381-1169

VL - 271

SP - 86

EP - 88

JO - Journal of Molecular Catalysis A: Chemical

JF - Journal of Molecular Catalysis A: Chemical

IS - 1-2

ER -

Novel quaternary ammoniumboronate salts as selective acylation catalysts

Abstract

Bibliographical note

Keywords

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