505 research outputs found
Additional file 3: of Combined femoral and sciatic nerve block versus femoral and local infiltration anesthesia for pain control after total knee arthroplasty: a meta-analysis of randomized controlled trials
The results of VAS with rest at 12 h, 24 h and 48 h after excluded the study of Safa B. (TIF 3014 kb
Additional file 1: of Combined femoral and sciatic nerve block versus femoral and local infiltration anesthesia for pain control after total knee arthroplasty: a meta-analysis of randomized controlled trials
The search strategy of the included studies. (DOCX 14 kb
<i>Vaccinia virus</i>, 33 strains, 17562 SNPs (increased).
<p><i>Vaccinia virus</i>, 33 strains, 17562 SNPs (increased).</p
Simple Branched Sulfur–Olefins as Chiral Ligands for Rh-Catalyzed Asymmetric Arylation of Cyclic Ketimines: Highly Enantioselective Construction of Tetrasubstituted Carbon Stereocenters
New, simple, sulfinamide-based branched olefin ligands
have been
developed and successfully used in Rh-catalyzed asymmetric arylations
of cyclic ketimines, providing efficient and highly enantioselective
access to valuable benzosultams and benzosulfamidates containing a
stereogenic quaternary carbon center. This is the first example of
applying a sulfur–olefin ligand in catalytic asymmetric addition
of imines
Evolutionary tree of <i>Burkholderia pseudomallei</i>.
<p>The internal nodes are labeled by the number of events, m for mutation, e for error, and x for HRE.</p
Summary of results from HREfinder and kSNP.
<p>Core SNPs are loci present in all the genomes. Homoplastic SNPs are those that are not consistent with the pattern of inheritance in the predicted SNP-based phylogeny.</p
Rhodium-Catalyzed Asymmetric Arylation of Cyclic <i>N</i>‑Sulfonyl Aryl Alkyl Ketimines: Efficient Access to Highly Enantioenriched α‑Tertiary Amines
A simple catalyst
system of RhÂ(I)/sulfur-olefin with exceptional
catalytic performance has been developed for the highly enantioselective
arylation of cyclic <i>N</i>-sulfonyl aryl alkyl ketimines
with arylboroxines/arylboronic acids. Optically active α-arylalkyl-substituted
benzosultams and benzosulfamidates which are generally difficult to
obtain were easily prepared with excellent stereocontrol (up to 99.9%
ee). The synthetic utility of the approach was demonstrated by the
facile construction of NMDA antagonist FR115427 and benzoxazinone
derivatives. This protocol offers new opportunities for the efficient
synthesis of diverse chiral α-tertiary amines
An example of detection of HREs.
<p>The SNPs on node 6 are better explained by an HRE from node 2 than inheritance from node 5 with three mutations. The first 2 A’s and last A do not represent SNPs, but merely serve as sequence context for the SNPs in between.</p
<i>Burkholderia mallei</i>, 11 strains, 3659 SNPs (increased).
<p><i>Burkholderia mallei</i>, 11 strains, 3659 SNPs (increased).</p
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