Results 161 to 170 of about 13,564 (218)
Decoding the hydrogen storage and functional properties of MgBH<sub>3</sub> (B = Mo and In) <i>via</i> first-principles simulations. [PDF]
Parves MS, Mia MH, Alsalmi O, Hasan MZ.
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Crystal structure of a π-conjugated N-donor ligand-bridged anionic bis-muth(III) iodide one-dimensional coordination polymer. [PDF]
Takahashi N, Endo Y, Sasaki H, Okubo T.
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Crystal structure of tris-[4-(3,4-di-meth-oxy-thio-phen-2-yl)phen-yl]amine. [PDF]
Yano M +4 more
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Cuticular Hydrocarbons-Revealed Functional Groups and Seasonal Acclimation in Sympatric Fig Wasp Mating Assemblages. [PDF]
Xie H +6 more
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Research reports on information sciences series C:Computer science C44
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Synthesis of 14C-Labeled FAD-C44
Journal of Labelled Compounds and Radiopharmaceuticals, 2000Synthesis of 14 C -labeled FAD-C44 1 al the tertiary carbon by the dimerization of 14 C labeled erucic acid 2 is described. Labeling at the C-14 position of erucic acid is achieved hy a convergent approach involving the Wittig coupling of 14 C-labeled nonyl aldehyde 4 and the Wittig reagent 3.
Christopher Bieniarz +2 more
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Synthesis of Deuterium Labeled FAD-C44
Journal of Labelled Compounds and Radiopharmaceuticals, 1999A concise synthetic methodology for selective deuterium labeling at the tertiary centers of the fatty acid dimer, FAD-C44 1 is described. Labeling methodology involves three steps and the deuterium is introduced at the tertiary carbons selectively by bromination of FAD-C44 followed by reduction with NaCNB2H3 and SnCl2.
Christopher Bieniarz +2 more
exaly +2 more sources
Synthetic Studies on Spongistatins: Synthesis of the C29–C44 Fragment
Tetrahedron Letters, 2000Abstract A convergent synthesis of the C29–C44 fragment, the common subunit of the spongipyran macrolides is described. The key step of the synthesis is the C -glycosidation reaction which is based on coupling of the lithiated F-ring sulfone with the E-ring aldehyde, and subsequent reductive desulfonylation to afford the E–F bis (pyran) with high ...
Michèle Guyot +2 more
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Synthetic Strategy Toward the C44–C65 Fragment of Mirabalin
Organic Letters, 2014A convergent and flexible stereoselective synthesis of one isomer of the C44-C65 fragment of mirabalin is described. The key steps include organocatalytic aldolization, ruthenium-catalyzed asymmetric hydrogenation, amide formation, Marshall stereoselective allenylation, and the Nozaki-Hiyama-Kishi reaction.
Sébastien Prévost +2 more
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