Zobrazeno 1 - 10
of 32
pro vyhledávání: '"H, Beierbeck"'
Molecular recognition XIV. Monte Carlo simulation of the hydration of the combining site of a Lectin
Publikováno v:
Canadian Journal of Chemistry. 72:463-470
Monte Carlo simulations of the hydration of the combining sites of the divalent lectin IV of Griffonia simplicifolia were carried out using the X-ray structure of the native lectin at 2.15 Å resolution. The regions of the combining sites are identic
Publikováno v:
Canadian Journal of Chemistry. 70:241-253
The relative potencies of both the monodeoxy and mono-O-methyl derivatives of the Leb-OMe tetrasaccharide (α-L-Fuc-(1 → 2)-β-D-Gal-(1 → 3)-[α-L-Fuc-(1 → 4)]-β-D-GlcNAc-OMe) as inhibitors of the complexation of a Leb artificial antigen by th
Publikováno v:
Ciba Foundation Symposium 158-Host-Guest Molecular Interactions: From Chemistry to Biology
As predicted by inhibition studies the X-ray crystal structure of the complex formed between the tetrasaccharide alpha-L-Fuc(1----2)-beta-D-Gal(1----3) [alpha-L-Fuc-(1----4)]-beta-D-GlcNAc- OMe (Leb-OMe) and the lectin IV of Griffonia simplicifolia (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b91a50772d45e80a0241fdccd75df064
https://doi.org/10.1002/9780470514085.ch15
https://doi.org/10.1002/9780470514085.ch15
Publikováno v:
Ciba Foundation symposium. 158
As predicted by inhibition studies the X-ray crystal structure of the complex formed between the tetrasaccharide alpha-L-Fuc(1----2)-beta-D-Gal(1----3) [alpha-L-Fuc-(1----4)]-beta-D-GlcNAc- OMe (Leb-OMe) and the lectin IV of Griffonia simplicifolia (
Autor:
J. K. Saunders, H. Beierbeck
Publikováno v:
Canadian Journal of Chemistry. 54:632-641
The effect of a heterosubstituent X on 13C chemical shifts, in conformations characterized by dihedral angles of 60°, is analyzed in terms of α-shifts, heteroatom–carbon (XC), hydrogen–heteroatom (HX) and carbon–heteroatom (CX) gauche interac
Autor:
J. K. Saunders, H. Beierbeck
Publikováno v:
Canadian Journal of Chemistry. 53:1307-1313
Carbon-13 chemical shifts in saturated hydrocarbons of staggered conformation may be derived from the corresponding resonances in ethane, propane, isobutane, and neopentane in the following way: every H—C—C(α)—C(β) gauche interaction between
Publikováno v:
Canadian Journal of Chemistry. 49:1335-1338
The calculation of chemical shift values by the method used in parts I–V (1–5) has been extended to a derivation of the shielding effects of the ethylene–ketal and −thioketal groups. For these studies ketal and thioketal derivatives of monoke
Autor:
H. Beierbeck, John W. ApSimon
Publikováno v:
Tetrahedron Letters. 14:581-584
Publikováno v:
Canadian Journal of Chemistry. 50:2351-2356
Using the methods described in parts I–VI of this series, we have examined the long-range shielding effects of the cyano group upon the C-18 and -19 methyl protons in several cyano-steroids and the ring protons in 2-endo- and 2-exo-cyanonorbornenes
Autor:
P. GENESTE, J. L. OLIVE, S. N. UNG, M. EL AMOUDI EL FAGHI, J. W. EASTON, H. BEIERBECK, J. K. SAUNDERS
Publikováno v:
Chemischer Informationsdienst. 10