Conformationally superarmed S-ethyl glycosyl donors as effective building blocks for chemoselective oligosaccharide synthesis in one pot

Mithila D. Bandara; Jagodige P. Yasomanee; Nigam P. Rath; Christian Marcus Pedersen; Mikael Bols; Alexei V. Demchenko

doi:10.1039/c6ob02498j

Conformationally superarmed S-ethyl glycosyl donors as effective building blocks for chemoselective oligosaccharide synthesis in one pot

Mithila D. Bandara, Jagodige P. Yasomanee, Nigam P. Rath, Christian Marcus Pedersen, Mikael Bols, Alexei V. Demchenko

Kemisk Institut

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review

17 Citationer (Scopus)

208 Downloads (Pure)

Abstract

A new series of superarmed glycosyl donors has been investigated. It was demonstrated that the S-ethyl leaving group allows for high reactivity, which is much higher than that of equally equipped S-phenyl glycosyl donors that were previously investigated by our groups. The superarmed S-ethyl glycosyl donors equipped with a 2-O-benzoyl group gave complete β-stereoselectivity. Utility of the new glycosyl donors has been demonstrated in a one-pot one-addition oligosaccharide synthesis with all of the reaction components present from the beginning

Originalsprog	Engelsk
Tidsskrift	Organic & Biomolecular Chemistry
Vol/bind	15
Udgave nummer	3
Sider (fra-til)	559-563
Antal sider	5
ISSN	1477-0520
DOI	https://doi.org/10.1039/c6ob02498j
Status	Udgivet - 2017

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10.1039/c6ob02498jLicens: CC BY

c6ob02498jForlagets udgivne version, 1,56 MBLicens: CC BY

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Citationsformater

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title = "Conformationally superarmed S-ethyl glycosyl donors as effective building blocks for chemoselective oligosaccharide synthesis in one pot",

abstract = "A new series of superarmed glycosyl donors has been investigated. It was demonstrated that the S-ethyl leaving group allows for high reactivity, which is much higher than that of equally equipped S-phenyl glycosyl donors that were previously investigated by our groups. The superarmed S-ethyl glycosyl donors equipped with a 2-O-benzoyl group gave complete β-stereoselectivity. Utility of the new glycosyl donors has been demonstrated in a one-pot one-addition oligosaccharide synthesis with all of the reaction components present from the beginning",

author = "Bandara, {Mithila D.} and Yasomanee, {Jagodige P.} and Rath, {Nigam P.} and Pedersen, {Christian Marcus} and Mikael Bols and Demchenko, {Alexei V.}",

year = "2017",

doi = "10.1039/c6ob02498j",

language = "English",

volume = "15",

pages = "559--563",

journal = "Organic & Biomolecular Chemistry",

issn = "1477-0520",

publisher = "Royal Society of Chemistry",

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TY - JOUR

T1 - Conformationally superarmed S-ethyl glycosyl donors as effective building blocks for chemoselective oligosaccharide synthesis in one pot

AU - Bandara, Mithila D.

AU - Yasomanee, Jagodige P.

AU - Rath, Nigam P.

AU - Pedersen, Christian Marcus

AU - Bols, Mikael

AU - Demchenko, Alexei V.

PY - 2017

Y1 - 2017

N2 - A new series of superarmed glycosyl donors has been investigated. It was demonstrated that the S-ethyl leaving group allows for high reactivity, which is much higher than that of equally equipped S-phenyl glycosyl donors that were previously investigated by our groups. The superarmed S-ethyl glycosyl donors equipped with a 2-O-benzoyl group gave complete β-stereoselectivity. Utility of the new glycosyl donors has been demonstrated in a one-pot one-addition oligosaccharide synthesis with all of the reaction components present from the beginning

AB - A new series of superarmed glycosyl donors has been investigated. It was demonstrated that the S-ethyl leaving group allows for high reactivity, which is much higher than that of equally equipped S-phenyl glycosyl donors that were previously investigated by our groups. The superarmed S-ethyl glycosyl donors equipped with a 2-O-benzoyl group gave complete β-stereoselectivity. Utility of the new glycosyl donors has been demonstrated in a one-pot one-addition oligosaccharide synthesis with all of the reaction components present from the beginning

U2 - 10.1039/c6ob02498j

DO - 10.1039/c6ob02498j

M3 - Journal article

C2 - 27942674

SN - 1477-0520

VL - 15

SP - 559

EP - 563

JO - Organic & Biomolecular Chemistry

JF - Organic & Biomolecular Chemistry

IS - 3

ER -