Zobrazeno 1 - 10
of 75
pro vyhledávání: '"S. McGavin"'
Autor:
Christopher J. Hanrahan, Christine L. Abraham, Christopher L. Peters, Neal K. Bangerter, Lance S. McGavin, Andrew E. Anderson, Alex J. Drew
Publikováno v:
Journal of Magnetic Resonance Imaging. 42:1329-1338
Purpose To deploy and quantify the accuracy of 3D dual echo steady state (DESS) MR arthrography with hip traction to image acetabular cartilage. Clinical magnetic resonance imaging (MRI) sequences used to image hip cartilage often have reduced out-of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::abe729bcf48cb26a9bdb624186144c81
https://doi.org/10.1002/jmri.24902
https://doi.org/10.1002/jmri.24902
Autor:
Christine L, Abraham, Neal K, Bangerter, Lance S, McGavin, Christopher L, Peters, Alex J, Drew, Christopher J, Hanrahan, Andrew E, Anderson
Publikováno v:
Journal of magnetic resonance imaging : JMRI. 42(5)
To deploy and quantify the accuracy of 3D dual echo steady state (DESS) MR arthrography with hip traction to image acetabular cartilage. Clinical magnetic resonance imaging (MRI) sequences used to image hip cartilage often have reduced out-of-plane r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::a3bb714554ea7147776a0c02ab4dadf6
https://pubmed.ncbi.nlm.nih.gov/25851109
https://pubmed.ncbi.nlm.nih.gov/25851109
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
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.