Synthesis of β-C-Galactosyl Ceramide and Its New Aza Variant via the Horner–Wadsworth

Synthesis of β-C-Galactosyl Ceramide and Its New Aza Variant via the Horner–Wadsworth–Emmons Reaction

Published:2014-05-15 Issue:11 Volume:79 Page:5193-5200
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Gorantla Jaggaiah N.¹²,Lankalapalli Ravi S.¹²

Affiliation:

1. Academy of Scientific and Innovative Research (AcSIR), New Delhi 110001, India

2. Agroprocessing and Natural Products Division, CSIR-National Institute for Interdisciplinary Science and Technology, Thiruvananthapuram 695019, Kerala, India

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo500769f

Reference33 articles.

1. Glycosphingolipids: synthesis and functions

2. Biological roles of oligosaccharides: all of the theories are correct

3. Inhibition of Entry of HIV-1 in Neural Cell Lines by Antibodies Against Galactosyl Ceramide

4. Galactosyl ceramide (or a closely related molecule) is the receptor for human immunodeficiency virus type 1 on human colon epithelial HT29 cells

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