10 research outputs found
Winterteelt komkommers, 1961-1962
<p><b>Copyright information:</b></p><p>Taken from "Mitochondrial sequences help to resolve deep phylogenetic relationships in rosids"</p><p>http://www.biomedcentral.com/1471-2148/7/217</p><p>BMC Evolutionary Biology 2007;7():217-217.</p><p>Published online 10 Nov 2007</p><p>PMCID:PMC2222252.</p><p></p>rcentages >50. For nodes where ML and MP analyses differ in topology, only the ML BS percentages are shown; asterisks denote contradictory resolutions between ML tree and MP strict consensus of all shortest trees
Copper-Catalyzed Oxidative Cyclization of Alkynes with Sulfonylhydrazides Leading to 2‑Sulfonated 9<i>H</i>‑pyrroloÂ[1,2‑<i>a</i>]Âindol-9-ones
A copper-catalyzed oxidative cyclization
procedure has been developed
for the production of 2-sulfonated 9<i>H</i>-pyrroloÂ[1,2-<i>a</i>]Âindol-9-ones via the direct sulfonylation of <i>N</i>-propargyl-substituted indoles with sulfonylÂhydrazides and <i>tert</i>-butyl hydroperoxide (TBHP). This novel protocol, which
tolerates a broad range of functional groups, offers a simple, efficient,
and atom-economical route to a series of fluorazones in good yields
under mild conditions
Synthesis of Organophosphorus Compounds through Copper-Catalyzed Annulation Involving C–O and C–P Bond Formations
A novel copperÂ(II) trifluoromethanesulfonate-catalyzed,
high-efficiency,
and atom-economical synthesis of valuable organophosphorus compounds
via cascade annulation of propargylic alcohols with diphenylphosphine
oxide is described. This protocol, which has a good functional-group
compatibility and insensitivity to an ambient atmosphere, provides
a simple and direct pathway to the products, organophosphorus compounds,
in good yields under mild conditions. The method could be efficiently
scaled up to gram scale, thus highlighting a potential application
of this methodology
Lewis Acid Catalyzed Dehydrogenative Coupling of Tertiary Propargylic Alcohols with Quinoline <i>N</i>‑Oxides
An unprecedented Lewis acid catalyzed,
high-efficiency synthesis
of valuable 2-(quinolin-2-yl)Âprop-2-en-1-ones via dehydrogenative
coupling of propargylic alkynols with quinoline <i>N</i>-oxides is described. This protocol, which tolerates a broad range
of functional groups, provides a straightforward pathway to the products
2-(quinolin-2-yl)Âprop-2-en-1-one scaffolds in satisfactory yields.
The conversion could be scaled up to gram scale efficiently, which
underlines a latent application of this methodology
Lewis Acid Catalyzed Cyclization of Propargylic Alcohols with 2‑Vinylphenol
An unprecedented
Lewis acid catalyzed, protection-free, and high-efficiency
synthesis of valuable 3,4-dihydro-2<i>H</i>-2,4-methanochromans
via cycloaddition of propargylic alkynols with 2-vinylphenol is described.
This cycloaddition protocol, which tolerates a wide variety of functional
groups, provides practical, versatile, and atom-economical access
to a new class of appealing bridged-ring products in satisfactory
yields. Compared with the reported reaction conditions for bridged-ring
skeletons synthesis, the present reaction conditions are neutral,
mild, and without any additives
AgSCF<sub>3</sub>‑Mediated Trifluoromethylthiolation/Radical Cascade Cyclization of 1,6-Enynes
A AgSCF<sub>3</sub>-mediated radical cascade cyclization/trifluoromethylthiolation
of 1,6-enynes triggered by a C–C triple bond is developed.
This protocol also provides another opportunity to construct a valuable
trifluoromethylthio-substituted polycyclic fluorene system through
the formations of one C–SCF<sub>3</sub> bond and two C–C
bonds in a single step
BF<sub>3</sub>·OEt<sub>2</sub>‑AgSCF<sub>3</sub> Mediated TrifluoroÂmethylÂthiolation/Cascade Cyclization of Propynols: Synthesis of 4‑((TrifluoroÂmethyl)Âthio)‑2<i>H</i>‑chromene and 4‑((TrifluoroÂmethyl)Âthio)-1,2-dihydroÂquinoline Derivatives
A BF<sub>3</sub>·OEt<sub>2</sub>–AgSCF<sub>3</sub> mediated
direct trifluoroÂmethylÂthiolation/cascade cyclization of
propynols involving the SCF<sub>3</sub> anion nucleophilic pathway
is developed. This protocol also provides an opportunity to construct
valuable trifluoromethylthio-substituted 2<i>H</i>-chromene
and 1,2-dihydroquinoline systems with high efficiency under mild conditions.
Additionally, the developed BF<sub>3</sub>·OEt<sub>2</sub>–AgSCF<sub>3</sub> reaction system could be scaled up to gram quantities in
a satisfactory yield without inert gas protection
Additional file 2: of Medical expenses of urban Chinese patients with stomach cancer during 2002–2011: a hospital-based multicenter retrospective study
Table S1. Medical expenses for stomach cancer diagnosis and treatment per patient by stage and therapy (average expenses, 95%CI). (DOCX 15Ă‚Â kb
Additional file 3: of Medical expenses of urban Chinese patients with stomach cancer during 2002–2011: a hospital-based multicenter retrospective study
Table S2. Generalized linear model (GLM)-Gamma regression model. (DOCX 18Ă‚Â kb
Additional file 1: of Medical expenses of urban Chinese patients with stomach cancer during 2002–2011: a hospital-based multicenter retrospective study
Figure S1. Yearly trend of medical expense for stomach cancer diagnosis and treatment per patient, by province groups, 2002-2011 . A to B show the yearly trend of medical expense per patient by province (A), by data reliability (B). (PDF 418 kb