Indium triflate mediated acetalization of aldehydes and ketones

Brendan M. Smith; Andrew E. Graham

doi:10.1016/j.tetlet.2006.10.111

Indium triflate mediated acetalization of aldehydes and ketones

Brendan M. Smith, Andrew E. Graham^*

^*Corresponding author for this work

Faculty of Computing, Engineering and Science

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

40 Citations (Scopus)

Abstract

Aldehydes and ketones are rapidly transformed into either acyclic or cyclic acetals at room temperature in high yields and in very short reaction times using catalytic quantities of indium triflate, in contrast to previous reports.

Original language	English
Pages (from-to)	9317-9319
Number of pages	3
Journal	Tetrahedron Letters
Volume	47
Issue number	52
DOIs	https://doi.org/10.1016/j.tetlet.2006.10.111
Publication status	Published - 25 Dec 2006

Keywords

Acetalization
Indium triflate

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10.1016/j.tetlet.2006.10.111Licence: CC BY-NC-ND

40 Citations
1 Doctoral Thesis

The Utilisation of Indium(III) Salts as Highly Efficient Catalysts in Organic Synthesis
Smith, B., 2008
Research output: Types of Thesis › Doctoral Thesis

Cite this

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title = "Indium triflate mediated acetalization of aldehydes and ketones",

abstract = "Aldehydes and ketones are rapidly transformed into either acyclic or cyclic acetals at room temperature in high yields and in very short reaction times using catalytic quantities of indium triflate, in contrast to previous reports. ",

keywords = "Acetalization, Indium triflate",

author = "Smith, {Brendan M.} and Graham, {Andrew E.}",

year = "2006",

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journal = "Tetrahedron Letters",

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T1 - Indium triflate mediated acetalization of aldehydes and ketones

AU - Smith, Brendan M.

AU - Graham, Andrew E.

PY - 2006/12/25

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N2 - Aldehydes and ketones are rapidly transformed into either acyclic or cyclic acetals at room temperature in high yields and in very short reaction times using catalytic quantities of indium triflate, in contrast to previous reports.

AB - Aldehydes and ketones are rapidly transformed into either acyclic or cyclic acetals at room temperature in high yields and in very short reaction times using catalytic quantities of indium triflate, in contrast to previous reports.

KW - Acetalization

KW - Indium triflate

U2 - 10.1016/j.tetlet.2006.10.111

DO - 10.1016/j.tetlet.2006.10.111

M3 - Article

AN - SCOPUS:33751176464

SN - 1873-3581

VL - 47

SP - 9317

EP - 9319

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 52

ER -

Indium triflate mediated acetalization of aldehydes and ketones

Abstract

Keywords

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Research output

The Utilisation of Indium(III) Salts as Highly Efficient Catalysts in Organic Synthesis

Cite this