Indium(III) triflate catalysed transacetalisation reactions of diols and triols under solvent-free conditions

Brendan M. Smith; Tomasz M. Kubczyk; Andrew E. Graham

doi:10.1016/j.tet.2012.07.048

Indium(III) triflate catalysed transacetalisation reactions of diols and triols under solvent-free conditions

Brendan M. Smith, Tomasz M. Kubczyk, Andrew E. Graham^*

^*Awdur cyfatebol y gwaith hwn

Cyfadran Cyfrifiadureg, Peirianneg a Gwyddoniaeth

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

11 Dyfyniadau (Scopus)

Crynodeb

Acyclic acetals and ketals undergo transacetalisation in the presence of catalytic quantities of indium(III) triflate (In(OTf) ₃) and diols or triols under solvent-free conditions to generate the corresponding cyclic acetals and ketals in excellent yield. The methodology has been further developed to encompass a tandem acetalisation-acetal exchange protocol, which provides a facile and high yielding route to cyclic ketals from unreactive ketones under very mild reaction conditions.

Iaith wreiddiol	Saesneg
Tudalennau (o-i)	7775-7781
Nifer y tudalennau	7
Cyfnodolyn	Tetrahedron Letters
Cyfrol	68
Rhif cyhoeddi	38
Dynodwyr Gwrthrych Digidol (DOIs)	https://doi.org/10.1016/j.tet.2012.07.048
Statws	Cyhoeddwyd - 23 Medi 2012

Mynediad at Ddogfen

10.1016/j.tet.2012.07.048Trwydded: CC BY-NC-ND

11 Dyfyniadau
1 Thesis Doethurol

The Utilisation of Indium(III) Salts as Highly Efficient Catalysts in Organic Synthesis
Smith, B., 2008
Allbwn ymchwil: Mathau o Thesis › Thesis Doethurol

Dyfynnu hyn

@article{415a6cce02c147998cdce9940a549e03,

title = "Indium(III) triflate catalysed transacetalisation reactions of diols and triols under solvent-free conditions",

abstract = "Acyclic acetals and ketals undergo transacetalisation in the presence of catalytic quantities of indium(III) triflate (In(OTf) 3) and diols or triols under solvent-free conditions to generate the corresponding cyclic acetals and ketals in excellent yield. The methodology has been further developed to encompass a tandem acetalisation-acetal exchange protocol, which provides a facile and high yielding route to cyclic ketals from unreactive ketones under very mild reaction conditions. ",

keywords = "Glycerol valorisation, Indium(III) triflate, Solvent-free reactions, Tandem reaction protocol, Transacetalisation",

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

year = "2012",

month = sep,

day = "23",

doi = "10.1016/j.tet.2012.07.048",

language = "English",

volume = "68",

pages = "7775--7781",

journal = "Tetrahedron Letters",

issn = "0040-4039",

publisher = "Elsevier",

number = "38",

}

TY - JOUR

T1 - Indium(III) triflate catalysed transacetalisation reactions of diols and triols under solvent-free conditions

AU - Smith, Brendan M.

AU - Kubczyk, Tomasz M.

AU - Graham, Andrew E.

PY - 2012/9/23

Y1 - 2012/9/23

N2 - Acyclic acetals and ketals undergo transacetalisation in the presence of catalytic quantities of indium(III) triflate (In(OTf) 3) and diols or triols under solvent-free conditions to generate the corresponding cyclic acetals and ketals in excellent yield. The methodology has been further developed to encompass a tandem acetalisation-acetal exchange protocol, which provides a facile and high yielding route to cyclic ketals from unreactive ketones under very mild reaction conditions.

AB - Acyclic acetals and ketals undergo transacetalisation in the presence of catalytic quantities of indium(III) triflate (In(OTf) 3) and diols or triols under solvent-free conditions to generate the corresponding cyclic acetals and ketals in excellent yield. The methodology has been further developed to encompass a tandem acetalisation-acetal exchange protocol, which provides a facile and high yielding route to cyclic ketals from unreactive ketones under very mild reaction conditions.

KW - Glycerol valorisation

KW - Indium(III) triflate

KW - Solvent-free reactions

KW - Tandem reaction protocol

KW - Transacetalisation

U2 - 10.1016/j.tet.2012.07.048

DO - 10.1016/j.tet.2012.07.048

M3 - Article

AN - SCOPUS:84864584384

SN - 0040-4039

VL - 68

SP - 7775

EP - 7781

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 38

ER -

Indium(III) triflate catalysed transacetalisation reactions of diols and triols under solvent-free conditions

Crynodeb

Mynediad at Ddogfen

Ôl bys

Allbwn Ymchwil

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

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