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^*

^*Awdur cyfatebol y gwaith hwn

Cyfadran Cyfrifiadureg, Peirianneg a Gwyddoniaeth

Allbwn ymchwil: Cyfraniad at gyfnodolyn › Erthygl › adolygiad gan gymheiriaid

40 Dyfyniadau (Scopus)

Crynodeb

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.

Iaith wreiddiol	Saesneg
Tudalennau (o-i)	9317-9319
Nifer y tudalennau	3
Cyfnodolyn	Tetrahedron Letters
Cyfrol	47
Rhif cyhoeddi	52
Dynodwyr Gwrthrych Digidol (DOIs)	https://doi.org/10.1016/j.tetlet.2006.10.111
Statws	Cyhoeddwyd - 25 Rhag 2006

Mynediad at Ddogfen

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

Dyfynnu hyn

@article{4a9d65a7e70444cd911a8f7aad832e51,

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",

month = dec,

day = "25",

doi = "10.1016/j.tetlet.2006.10.111",

language = "English",

volume = "47",

pages = "9317--9319",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier",

number = "52",

}

TY - JOUR

T1 - Indium triflate mediated acetalization of aldehydes and ketones

AU - Smith, Brendan M.

AU - Graham, Andrew E.

PY - 2006/12/25

Y1 - 2006/12/25

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

VL - 47

SP - 9317

EP - 9319

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 52

ER -

Indium triflate mediated acetalization of aldehydes and ketones

Crynodeb

Mynediad at Ddogfen

Ôl bys

Dyfynnu hyn