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

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Standard

Conformationally superarmed S-ethyl glycosyl donors as effective building blocks for chemoselective oligosaccharide synthesis in one pot. / Bandara, Mithila D.; Yasomanee, Jagodige P.; Rath, Nigam P.; Pedersen, Christian Marcus; Bols, Mikael; Demchenko, Alexei V.

I: Organic & Biomolecular Chemistry, Bind 15, Nr. 3, 2017, s. 559-563.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Bandara, MD, Yasomanee, JP, Rath, NP, Pedersen, CM, Bols, M & Demchenko, AV 2017, 'Conformationally superarmed S-ethyl glycosyl donors as effective building blocks for chemoselective oligosaccharide synthesis in one pot', Organic & Biomolecular Chemistry, bind 15, nr. 3, s. 559-563. https://doi.org/10.1039/c6ob02498j

APA

Bandara, M. D., Yasomanee, J. P., Rath, N. P., Pedersen, C. M., Bols, M., & Demchenko, A. V. (2017). Conformationally superarmed S-ethyl glycosyl donors as effective building blocks for chemoselective oligosaccharide synthesis in one pot. Organic & Biomolecular Chemistry, 15(3), 559-563. https://doi.org/10.1039/c6ob02498j

Vancouver

Bandara MD, Yasomanee JP, Rath NP, Pedersen CM, Bols M, Demchenko AV. Conformationally superarmed S-ethyl glycosyl donors as effective building blocks for chemoselective oligosaccharide synthesis in one pot. Organic & Biomolecular Chemistry. 2017;15(3):559-563. https://doi.org/10.1039/c6ob02498j

Author

Bandara, Mithila D. ; Yasomanee, Jagodige P. ; Rath, Nigam P. ; Pedersen, Christian Marcus ; Bols, Mikael ; Demchenko, Alexei V. / Conformationally superarmed S-ethyl glycosyl donors as effective building blocks for chemoselective oligosaccharide synthesis in one pot. I: Organic & Biomolecular Chemistry. 2017 ; Bind 15, Nr. 3. s. 559-563.

Bibtex

@article{122432cae2324e108a6e5ec1621218fa,
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",
number = "3",

}

RIS

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

VL - 15

SP - 559

EP - 563

JO - Organic & Biomolecular Chemistry

JF - Organic & Biomolecular Chemistry

SN - 1477-0520

IS - 3

ER -

ID: 176368495