Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Robert S. McGavin"'
Publikováno v:
Tetrahedron: Asymmetry. 10:17-20
A hydroxyl protected tetrasaccharide intermediate, corresponding to a segment of the rhamnogalacturonan I polysaccharide, has been synthesized using the glycosyl imidate technique. This tetrasaccharide is designed to allow for further elongation and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79a5036cf37b3f9542f645bd5551c38b
https://doi.org/10.1016/s0957-4166(98)00494-7
https://doi.org/10.1016/s0957-4166(98)00494-7
Publikováno v:
ChemInform. 30
A hydroxyl protected tetrasaccharide intermediate, corresponding to a segment of the rhamnogalacturonan I polysaccharide, has been synthesized using the glycosyl imidate technique. This tetrasaccharide is designed to allow for further elongation and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6325006db5fbd427f9db4ecb181fa4f0
https://doi.org/10.1002/chin.199923236
https://doi.org/10.1002/chin.199923236
Publikováno v:
ChemInform. 32
The synthesis of a versatile l -rhamnose monosaccharide synthon is described. This synthon is used in the synthesis of a disaccharide containing the rare sugar, 6-deoxy- l -glucose, linked to the 3-C-hydroxymethyl group of methyl 2,3-O-isopropylidene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1c75f10fe017ef07dedafbb862a54b7e
https://doi.org/10.1002/chin.200126199
https://doi.org/10.1002/chin.200126199
Autor:
Robert S. McGavin, Todd L. Lowary
Publikováno v:
e-EROS Encyclopedia of Reagents for Organic Synthesis
[132799-16-7] C17H22F3IN2O3S (MW 518.33) InChI = 1S/2C8H11N.CHF3O3S.H2I/c2*1-6-4-7(2)9-8(3)5-6;2-1(3,4)8(5,6)7;/h2*4-5H,1-3H3;(H,5,6,7);1H2/q;;;+1/p-1 InChIKey = NHMJWSHZUNSWPD-UHFFFAOYSA-M (convenient source of iodonium ion, effective in activation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::871baf0e9a4a7a29a62550bd4db69694
https://doi.org/10.1002/047084289x.rn00536
https://doi.org/10.1002/047084289x.rn00536
Publikováno v:
Carbohydrate research. 339(15)
A disaccharide portion of the A-side chain of the rhamnogalacturonan II oligosaccharide has been prepared. Glycosylation of methyl (methyl 3,4- O -isopropylidene-α- d -galactopyranosid)uronate with p -tolyl 2,3-di- O -acetyl-3- C -(benzyloxymethyl)-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77a6212e821b1e4aee21621635af8343
https://pubmed.ncbi.nlm.nih.gov/15476711
https://pubmed.ncbi.nlm.nih.gov/15476711
Autor:
Rodney A. Gagne, Pavel I. Kitov, Mary C. Chervenak, Robert S. McGavin, Michael Warwas, Ping Zhang, Robert B. Mario Pinto, Chang-Chun Ling, David R. Bundle, Ramon Alibes
Publikováno v:
XXIst International Carbohydrate Symposium 2002.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64b0351eb3120b1ec050567a49abf64f
https://doi.org/10.1100/tsw.2002.356
https://doi.org/10.1100/tsw.2002.356
Publikováno v:
Carbohydrate research. 330(4)
The synthesis of a versatile l -rhamnose monosaccharide synthon is described. This synthon is used in the synthesis of a disaccharide containing the rare sugar, 6-deoxy- l -glucose, linked to the 3-C-hydroxymethyl group of methyl 2,3-O-isopropylidene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3162222c2684382a195490a22f98f9a
https://pubmed.ncbi.nlm.nih.gov/11269404
https://pubmed.ncbi.nlm.nih.gov/11269404
Publikováno v:
Organic & Biomolecular Chemistry. 3:2723
Carbohydrate–protein interactions have been investigated for a model system of a monoclonal antibody, SYA/J6, which binds a trisaccharide epitope of the O-polysaccharide of the Shigella flexneri variant Y lipopolysaccharide. The thermodynamics of b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bede517e87193ce94a8f96782f704263
https://doi.org/10.1039/b416105j
https://doi.org/10.1039/b416105j