Nucleophilic cationization reagents

Souvik Biswas; Xuan Huang; Wesley R. Badger; Michael H. Nantz

doi:10.1016/j.tetlet.2010.01.094

Nucleophilic cationization reagents

Souvik Biswas, Xuan Huang, Wesley R. Badger, Michael H. Nantz

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

23 Scopus citations

Abstract

Nucleophilic cationization reagents fitted with aminooxy groups are described. Practical syntheses of mono- and bis-aminooxy tetraalkylammonium iodides including N-hydroxyethyl-functionalized analogs are reported. An oximation example using one of the reagents is presented to illustrate their use in synthesis of cationic materials.

Original language	English (US)
Pages (from-to)	1727-1729
Number of pages	3
Journal	Tetrahedron Letters
Volume	51
Issue number	13
DOIs	https://doi.org/10.1016/j.tetlet.2010.01.094
State	Published - Mar 31 2010
Externally published	Yes

ASJC Scopus subject areas

Biochemistry
Organic Chemistry
Drug Discovery

Access to Document

10.1016/j.tetlet.2010.01.094

Cite this

@article{f9f2f56f1f5a48e6a58e60ece7296a51,

title = "Nucleophilic cationization reagents",

abstract = "Nucleophilic cationization reagents fitted with aminooxy groups are described. Practical syntheses of mono- and bis-aminooxy tetraalkylammonium iodides including N-hydroxyethyl-functionalized analogs are reported. An oximation example using one of the reagents is presented to illustrate their use in synthesis of cationic materials.",

author = "Souvik Biswas and Xuan Huang and Badger, {Wesley R.} and Nantz, {Michael H.}",

year = "2010",

month = mar,

day = "31",

doi = "10.1016/j.tetlet.2010.01.094",

language = "English (US)",

volume = "51",

pages = "1727--1729",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier Limited",

number = "13",

}

TY - JOUR

T1 - Nucleophilic cationization reagents

AU - Biswas, Souvik

AU - Huang, Xuan

AU - Badger, Wesley R.

AU - Nantz, Michael H.

PY - 2010/3/31

Y1 - 2010/3/31

N2 - Nucleophilic cationization reagents fitted with aminooxy groups are described. Practical syntheses of mono- and bis-aminooxy tetraalkylammonium iodides including N-hydroxyethyl-functionalized analogs are reported. An oximation example using one of the reagents is presented to illustrate their use in synthesis of cationic materials.

AB - Nucleophilic cationization reagents fitted with aminooxy groups are described. Practical syntheses of mono- and bis-aminooxy tetraalkylammonium iodides including N-hydroxyethyl-functionalized analogs are reported. An oximation example using one of the reagents is presented to illustrate their use in synthesis of cationic materials.

UR - http://www.scopus.com/inward/record.url?scp=76949089967&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=76949089967&partnerID=8YFLogxK

U2 - 10.1016/j.tetlet.2010.01.094

DO - 10.1016/j.tetlet.2010.01.094

M3 - Article

AN - SCOPUS:76949089967

VL - 51

SP - 1727

EP - 1729

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 13

ER -

Nucleophilic cationization reagents

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this