Combinatorial chemistry of piperidine based carbohydrate mimics

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Standard

Combinatorial chemistry of piperidine based carbohydrate mimics. / Byrgesen, Elisabeth; Nielsen, John; Willert, Marianne; Bols, Mikael.

I: Tetrahedron Letters, Bind 38, Nr. 32, 01.08.1997, s. 5697-5700.

Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt

Harvard

Byrgesen, E, Nielsen, J, Willert, M & Bols, M 1997, 'Combinatorial chemistry of piperidine based carbohydrate mimics', Tetrahedron Letters, bind 38, nr. 32, s. 5697-5700. https://doi.org/10.1016/S0040-4039(97)01249-5

APA

Byrgesen, E., Nielsen, J., Willert, M., & Bols, M. (1997). Combinatorial chemistry of piperidine based carbohydrate mimics. Tetrahedron Letters, 38(32), 5697-5700. https://doi.org/10.1016/S0040-4039(97)01249-5

Vancouver

Byrgesen E, Nielsen J, Willert M, Bols M. Combinatorial chemistry of piperidine based carbohydrate mimics. Tetrahedron Letters. 1997 aug. 1;38(32):5697-5700. https://doi.org/10.1016/S0040-4039(97)01249-5

Author

Byrgesen, Elisabeth ; Nielsen, John ; Willert, Marianne ; Bols, Mikael. / Combinatorial chemistry of piperidine based carbohydrate mimics. I: Tetrahedron Letters. 1997 ; Bind 38, Nr. 32. s. 5697-5700.

Bibtex

@article{29a3239b65f6478b9c1fd9e56a29324f,
title = "Combinatorial chemistry of piperidine based carbohydrate mimics",
abstract = "Piperidine carboxylic acids and 4-hydroxypiperidine-3-carboxylic acid, the latter obtained from bakers yeast reduction of the corresponding piperidone, were coupled in solid-phase synthesis to form simplified oligosaccharide analogues. A split-and-mix synthesis approach was used to create small combinatorial libraries which were characterised by LC-MS and screened as inhibitors of glycosidases.",
author = "Elisabeth Byrgesen and John Nielsen and Marianne Willert and Mikael Bols",
year = "1997",
month = aug,
day = "1",
doi = "10.1016/S0040-4039(97)01249-5",
language = "English",
volume = "38",
pages = "5697--5700",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Pergamon Press",
number = "32",

}

RIS

TY - JOUR

T1 - Combinatorial chemistry of piperidine based carbohydrate mimics

AU - Byrgesen, Elisabeth

AU - Nielsen, John

AU - Willert, Marianne

AU - Bols, Mikael

PY - 1997/8/1

Y1 - 1997/8/1

N2 - Piperidine carboxylic acids and 4-hydroxypiperidine-3-carboxylic acid, the latter obtained from bakers yeast reduction of the corresponding piperidone, were coupled in solid-phase synthesis to form simplified oligosaccharide analogues. A split-and-mix synthesis approach was used to create small combinatorial libraries which were characterised by LC-MS and screened as inhibitors of glycosidases.

AB - Piperidine carboxylic acids and 4-hydroxypiperidine-3-carboxylic acid, the latter obtained from bakers yeast reduction of the corresponding piperidone, were coupled in solid-phase synthesis to form simplified oligosaccharide analogues. A split-and-mix synthesis approach was used to create small combinatorial libraries which were characterised by LC-MS and screened as inhibitors of glycosidases.

U2 - 10.1016/S0040-4039(97)01249-5

DO - 10.1016/S0040-4039(97)01249-5

M3 - Journal article

AN - SCOPUS:0030817956

VL - 38

SP - 5697

EP - 5700

JO - Tetrahedron Letters

JF - Tetrahedron Letters

SN - 0040-4039

IS - 32

ER -

ID: 131114868