Zobrazeno 1 - 10
of 106
pro vyhledávání: '"Hugh Chaplin"'
Publikováno v:
British Journal of Haematology. 48:69-78
A sensitive radiolabelled anti-antiglobulin method was devised and applied to quantitating red blood cell-bound C3d (RBC-C3d) in samples from 174 normal blood donors. C3d was demonstrable on all RBC examined; 98% of values fell over a broad range, wi
Publikováno v:
The Journal of Organic Chemistry. 73:1131-1134
A convenient method for the synthesis of 2-bromo-3-aroyl-benzo[b]furans from readily accessible precursors has been developed. The 2-bromo group has been employed as a versatile synthetic handle in both palladium-mediated couplings and direct nucleop
Although it has been shown that red cell viability can be maintained for at least two years by storage in glycerol at −79° C, there is a progressive loss of viability after six months of storage at −20° C. Because of the practical objections to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16ce53d2c1001fcc032edadfbb9453f2
https://doi.org/10.1159/000427126
https://doi.org/10.1159/000427126
Publikováno v:
Transfusion. 15:439-448
Hydroxyethyl starch (HES), which is licensed for human use as a plasma volume expander, has red blood cell sedimenting properties similar to high molecular weight dextran (HMWD). The present studies document the effectiveness of commercially availabl
Publikováno v:
ChemInform. 45
Reductive coupling of α,β-unsaturated acid chlorides A with alkynoyls B provides convergent access to Nazarov cyclization precursors, α-carboxy divinyl ketones C. Cyclization of C gives an intermediate oxyallyl cation intermediate D, which can be
Publikováno v:
The Journal of organic chemistry. 79(8)
Reductive coupling of α,β-unsaturated acid chlorides A with alkynoyls B provides convergent access to Nazarov cyclization precursors, α-carboxy divinyl ketones C. Cyclization of C gives an intermediate oxyallyl cation intermediate D, which can be
Publikováno v:
ChemInform. 43
In the presence of an excess of MesOH or TfOH, divinyl and aryl vinyl ketones bearing an oxazolidinone auxiliary undergo efficient and highly stereoselective cyclization to optically active cyclopentenone derivatives.
Publikováno v:
Organic letters. 14(7)
Oxazolidinones are powerful promoters of the Nazarov reaction, enabling the cyclization of conventionally resistant substrates to be achieved under mild conditions. They exert excellent regio- and torquoselective control in both the conventional Naza
Publikováno v:
Transfusion. 34:427-431
BACKGROUND: Several cold autoantibodies (usually IgG) with IT specificity have been reported previously, as have autoantibodies with joint I and P blood group specificities (IP1, ITP1, iP1, IP). A fatal outcome associated with an IgM cold autoantibod