Stereoselective synthesis of glycosides using (salen)Co catalysts as promoters

Sandra Medina; Alexander S Henderson; John F Bower; M Carmen Galan

doi:10.1039/c5cc02552d

Stereoselective synthesis of glycosides using (salen)Co catalysts as promoters

Sandra Medina , Alexander S Henderson, John F Bower, M Carmen Galan

Research output: Contribution to journal › Article (Academic Journal) › peer-review

24 Citations (Scopus)

348 Downloads (Pure)

Abstract

The use of (salen)Co catalysts as a new class of bench-stable stereoselective glycosylation promoters of trichloroacetimidate glycosyl donors at room temperature is described. The conditions are practical and do not require the use of molecular sieves with products being isolated in good to high yields.

Original language	English
Pages (from-to)	8939-8941
Number of pages	3
Journal	Chemical Communications
Volume	51
Issue number	43
Early online date	23 Apr 2015
DOIs	https://doi.org/10.1039/c5cc02552d
Publication status	Published - 30 Apr 2015

Structured keywords

BCS and TECS CDTs

Access to Document

10.1039/c5cc02552d

Stereoselective synthesis of glycosides using (salen)Co catalysts as promotersFinal published version, 1.38 MB

Handle.net

Persistent link

Catalytic stereoselective synthesis of glycosides
Galan, M. C.
1/07/13 → 1/07/15
Project: Research
3-month Core Capability for Chemistry Research
Crosby, J.
1/01/13 → 1/04/13
Project: Research
Reworking of Novel tools for Glycoscience
Galan, M. C.
31/03/12 → 30/08/17
Project: Research

Cite this

@article{83ac643b3af94012af35f81a2cff7a85,

title = "Stereoselective synthesis of glycosides using (salen)Co catalysts as promoters",

abstract = "The use of (salen)Co catalysts as a new class of bench-stable stereoselective glycosylation promoters of trichloroacetimidate glycosyl donors at room temperature is described. The conditions are practical and do not require the use of molecular sieves with products being isolated in good to high yields.",

author = "Sandra Medina and Henderson, {Alexander S} and Bower, {John F} and Galan, {M Carmen}",

year = "2015",

month = apr,

day = "30",

doi = "10.1039/c5cc02552d",

language = "English",

volume = "51",

pages = "8939--8941",

journal = "Chemical Communications",

issn = "1359-7345",

publisher = "Royal Society of Chemistry",

number = "43",

}

TY - JOUR

T1 - Stereoselective synthesis of glycosides using (salen)Co catalysts as promoters

AU - Medina , Sandra

AU - Henderson, Alexander S

AU - Bower, John F

AU - Galan, M Carmen

PY - 2015/4/30

Y1 - 2015/4/30

N2 - The use of (salen)Co catalysts as a new class of bench-stable stereoselective glycosylation promoters of trichloroacetimidate glycosyl donors at room temperature is described. The conditions are practical and do not require the use of molecular sieves with products being isolated in good to high yields.

AB - The use of (salen)Co catalysts as a new class of bench-stable stereoselective glycosylation promoters of trichloroacetimidate glycosyl donors at room temperature is described. The conditions are practical and do not require the use of molecular sieves with products being isolated in good to high yields.

U2 - 10.1039/c5cc02552d

DO - 10.1039/c5cc02552d

M3 - Article (Academic Journal)

C2 - 25925803

SN - 1359-7345

VL - 51

SP - 8939

EP - 8941

JO - Chemical Communications

JF - Chemical Communications

IS - 43

ER -

Stereoselective synthesis of glycosides using (salen)Co catalysts as promoters

Abstract

Structured keywords

Access to Document

Handle.net

Fingerprint

Projects

Catalytic stereoselective synthesis of glycosides

3-month Core Capability for Chemistry Research

Reworking of Novel tools for Glycoscience

Cite this