Acetalization catalyzed by reusable N-methylimidazole trifluoromethyl sulfonate

Ningning Liu; Xi Chen; Qingshan Zhang; Qinpei Wu

doi:10.6023/cjoc201403042

Acetalization catalyzed by reusable N-methylimidazole trifluoromethyl sulfonate

Ningning Liu
, Xi Chen
, Qingshan Zhang
, Qinpei Wu^*

^*Corresponding author for this work

School of Chemistry and Chemical Engineering

Beijing Institute of Technology

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

2 Citations (Scopus)

Abstract

A number of aldehydes and ketones are effectively converted to acetals in the presence of N-methylimidazole trifluoromethyl sulfonate. The catalyst can be readily recovered through filtration and reused with high activity.

Original language	English
Pages (from-to)	1364-1368
Number of pages	5
Journal	Chinese Journal of Organic Chemistry
Volume	34
Issue number	7
DOIs	https://doi.org/10.6023/cjoc201403042
Publication status	Published - Jul 2014

Keywords

Acetalization
Carbonyl
Imidazole

Access to Document

10.6023/cjoc201403042

Cite this

@article{9fbca04fe54b45f38946bd92450cc2eb,

title = "Acetalization catalyzed by reusable N-methylimidazole trifluoromethyl sulfonate",

abstract = "A number of aldehydes and ketones are effectively converted to acetals in the presence of N-methylimidazole trifluoromethyl sulfonate. The catalyst can be readily recovered through filtration and reused with high activity.",

keywords = "Acetalization, Carbonyl, Imidazole",

author = "Ningning Liu and Xi Chen and Qingshan Zhang and Qinpei Wu",

year = "2014",

month = jul,

doi = "10.6023/cjoc201403042",

language = "English",

volume = "34",

pages = "1364--1368",

journal = "Chinese Journal of Organic Chemistry",

issn = "0253-2786",

publisher = "Science Press",

number = "7",

}

TY - JOUR

T1 - Acetalization catalyzed by reusable N-methylimidazole trifluoromethyl sulfonate

AU - Liu, Ningning

AU - Chen, Xi

AU - Zhang, Qingshan

AU - Wu, Qinpei

PY - 2014/7

Y1 - 2014/7

N2 - A number of aldehydes and ketones are effectively converted to acetals in the presence of N-methylimidazole trifluoromethyl sulfonate. The catalyst can be readily recovered through filtration and reused with high activity.

AB - A number of aldehydes and ketones are effectively converted to acetals in the presence of N-methylimidazole trifluoromethyl sulfonate. The catalyst can be readily recovered through filtration and reused with high activity.

KW - Acetalization

KW - Carbonyl

KW - Imidazole

UR - https://www.scopus.com/pages/publications/84904888753

U2 - 10.6023/cjoc201403042

DO - 10.6023/cjoc201403042

M3 - Article

AN - SCOPUS:84904888753

SN - 0253-2786

VL - 34

SP - 1364

EP - 1368

JO - Chinese Journal of Organic Chemistry

JF - Chinese Journal of Organic Chemistry

IS - 7

ER -

Acetalization catalyzed by reusable N-methylimidazole trifluoromethyl sulfonate

Abstract

Keywords

Access to Document

Other files and links

Fingerprint

Cite this