Superarming of glycosyl donors by combined neighboring and conformational effects.

Mads Heuckendorff; Hemali D. Premathilake; Papapida Pornsuriyasak; Anders Ø. Madsen; Christian M. Pedersen; Mikael Bols; Alexei V. Demchenko

doi:10.1021/ol402371b

Superarming of glycosyl donors by combined neighboring and conformational effects.

Mads Heuckendorff
, Hemali D. Premathilake
, Papapida Pornsuriyasak
, Anders Ø. Madsen
, Christian M. Pedersen
, Mikael Bols
, Alexei V. Demchenko

University of Missouri-St. Louis

Research output: Contribution to journal › Article › peer-review

Original language	American English
Journal	Organic Letters
Volume	15
DOIs	https://doi.org/10.1021/ol402371b
State	Published - Sep 20 2013

Disciplines

Biochemistry
Organic Chemistry

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@article{879b4e3c931b4b418194a75e551def59,

title = "Superarming of glycosyl donors by combined neighboring and conformational effects.",

author = "Mads Heuckendorff and Premathilake, \{Hemali D.\} and Papapida Pornsuriyasak and Madsen, \{Anders {\O}.\} and Pedersen, \{Christian M.\} and Mikael Bols and Demchenko, \{Alexei V.\}",

note = "A novel glycosyl donor that combines the concepts of both conformational and electronic superarming has been synthesized. The reactivity and selectivity of the donor has been tested in competition experiments. Traditionally oligosaccharide synthesis relies on protective group manipulations and the use of orthogonal glycosylation methods, such as different types of glycosyl donors.",

year = "2013",

month = sep,

day = "20",

doi = "10.1021/ol402371b",

language = "American English",

volume = "15",

journal = "Organic Letters",

}

TY - JOUR

T1 - Superarming of glycosyl donors by combined neighboring and conformational effects.

AU - Heuckendorff, Mads

AU - Premathilake, Hemali D.

AU - Pornsuriyasak, Papapida

AU - Madsen, Anders Ø.

AU - Pedersen, Christian M.

AU - Bols, Mikael

AU - Demchenko, Alexei V.

N1 - A novel glycosyl donor that combines the concepts of both conformational and electronic superarming has been synthesized. The reactivity and selectivity of the donor has been tested in competition experiments. Traditionally oligosaccharide synthesis relies on protective group manipulations and the use of orthogonal glycosylation methods, such as different types of glycosyl donors.

PY - 2013/9/20

Y1 - 2013/9/20

UR - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3823551/

U2 - 10.1021/ol402371b

DO - 10.1021/ol402371b

M3 - Article

VL - 15

JO - Organic Letters

JF - Organic Letters

ER -

Superarming of glycosyl donors by combined neighboring and conformational effects.

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