Novel galactosyl donor with 2-naphthylmethyl (NAP) as the non-participating group at C-2 position: Efficient synthesis of α-galactosyl ceramide

Sirajud D. Khaja; Vipin Kumar; Misbah Ahmad; Jun Xue; Khushi L. Matta

doi:10.1016/j.tetlet.2010.06.071

Novel galactosyl donor with 2-naphthylmethyl (NAP) as the non-participating group at C-2 position: Efficient synthesis of α-galactosyl ceramide

Sirajud D. Khaja
, Vipin Kumar
, Misbah Ahmad
, Jun Xue
, Khushi L. Matta

Department of Chemical and Biological Engineering

Roswell Park Cancer Institute

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

16 Scopus citations

Abstract

Predominant α-linked products can be generated in glycosylation involving galactosyl trichloroacetimidate donors with 2-naphthylmethyl (NAP) as the non-participating group at C-2 position. The above-mentioned donor was successfully utilized for the synthesis of α-galactosyl ceramide.

Original language	English
Pages (from-to)	4411-4414
Number of pages	4
Journal	Tetrahedron Letters
Volume	51
Issue number	33
DOIs	https://doi.org/10.1016/j.tetlet.2010.06.071
State	Published - Aug 18 2010

Keywords

α-Galactosyl ceramide
2-Naphthylmethyl (NAP)
Glycans
Oligosaccharides

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10.1016/j.tetlet.2010.06.071

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title = "Novel galactosyl donor with 2-naphthylmethyl (NAP) as the non-participating group at C-2 position: Efficient synthesis of α-galactosyl ceramide",

abstract = "Predominant α-linked products can be generated in glycosylation involving galactosyl trichloroacetimidate donors with 2-naphthylmethyl (NAP) as the non-participating group at C-2 position. The above-mentioned donor was successfully utilized for the synthesis of α-galactosyl ceramide.",

keywords = "α-Galactosyl ceramide, 2-Naphthylmethyl (NAP), Glycans, Oligosaccharides",

author = "Khaja, \{Sirajud D.\} and Vipin Kumar and Misbah Ahmad and Jun Xue and Matta, \{Khushi L.\}",

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language = "English",

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journal = "Tetrahedron Letters",

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TY - JOUR

T1 - Novel galactosyl donor with 2-naphthylmethyl (NAP) as the non-participating group at C-2 position

T2 - Efficient synthesis of α-galactosyl ceramide

AU - Khaja, Sirajud D.

AU - Kumar, Vipin

AU - Ahmad, Misbah

AU - Xue, Jun

AU - Matta, Khushi L.

PY - 2010/8/18

Y1 - 2010/8/18

N2 - Predominant α-linked products can be generated in glycosylation involving galactosyl trichloroacetimidate donors with 2-naphthylmethyl (NAP) as the non-participating group at C-2 position. The above-mentioned donor was successfully utilized for the synthesis of α-galactosyl ceramide.

AB - Predominant α-linked products can be generated in glycosylation involving galactosyl trichloroacetimidate donors with 2-naphthylmethyl (NAP) as the non-participating group at C-2 position. The above-mentioned donor was successfully utilized for the synthesis of α-galactosyl ceramide.

KW - α-Galactosyl ceramide

KW - 2-Naphthylmethyl (NAP)

KW - Glycans

KW - Oligosaccharides

UR - https://www.scopus.com/pages/publications/77955416593

U2 - 10.1016/j.tetlet.2010.06.071

DO - 10.1016/j.tetlet.2010.06.071

M3 - Article

AN - SCOPUS:77955416593

SN - 0040-4039

VL - 51

SP - 4411

EP - 4414

JO - Tetrahedron Letters

JF - Tetrahedron Letters

IS - 33

ER -

Novel galactosyl donor with 2-naphthylmethyl (NAP) as the non-participating group at C-2 position: Efficient synthesis of α-galactosyl ceramide

Abstract

Keywords

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