<i>N</i>-Phenyl-[1,1'-biphen-yl]-2-carboxamide. [PDF]
Guerah NEH +4 more
europepmc +1 more source
Levosimendan Form I, C<sub>14</sub>H<sub>12</sub>N<sub>6</sub>O. [PDF]
Salazar JK +3 more
europepmc +1 more source
Mol-ecular and crystal structure of <i>catena</i>-poly[1-benzyl-[1,2,4]triazolo[1,5-<i>c</i>]quinazolin-1-ium-2,5-bis-(thiol-ate) [[aqua-sodium]-di-μ-aqua]]. [PDF]
Shishkina SV +5 more
europepmc +1 more source
Crystal structures of (<i>S</i>)-3-{1-[(4-chloro-phen-yl)sulfon-yl]piperidin-2-yl}pyridine, (<i>S</i>)-3-[1-(4-methyl-phen-yl)piperidin-2-yl]pyridine, (<i>S</i>)-3-{1-[(4-meth-oxy-phen-yl)sulfon-yl]piperidin-2-yl}pyridine and (<i>S</i>)-3-{1-[(3,4-di-methyl-phen-yl)sulfon-yl]piperidin-2-yl}pyridine. [PDF]
Okmanov RY +4 more
europepmc +1 more source
Diterpenoids. XXXIV. The C13 configuration of tetrahydroabienol
Tetrahydroabienol is a quasiracemic compound formed from C13 epimers.
Carman R.M., Zerner G.W.
core +5 more sources
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The chemical exchange method has been applied to the separation of the isotopes of carbon. Various exchange reactions have been tested, using counter-current flow in packed fractionation columns, and of these, the exchange between hydrogen cyanide gas and a solution of sodium cyanide in water has been found to be most efficient.
Clyde A. Hutchison +2 more
openaire +1 more source
Binding of terbium and cisplatin to C13* human ovarian cancer cells using time-resolved terbium luminescence [PDF]
Terbium (Tb3+) has been shown to increase the cellular accumulation and cytotoxicity of cisplatin in cisplatin-resistant human breast and ovarian cancer cells.
Robert G Canada
exaly +2 more sources
C13 cross-relaxation measurements
Bültmann S, Baum G, Dulya CM, et al. C13 cross-relaxation measurements. In: Heller KJ, Smith SL, eds. High-Energy Spin Physics: proceedings (AIP Conference Proceedings). Vol 343.
Bültmann, Stephen +13 more
openaire +3 more sources
Synthesis of the C1−C13 Fragment of Leucascandrolide A
Organic Letters, 2000[reaction: see text] The synthesis of the C1-C13 fragment 3 of leucascandrolide A has been completed utilizing a stereoselective and regioselective reductive cleavage of a highly functionalized spiroketal to incorporate the cis-2,6-disubstituted tetrahydropyan. The spiroketal was constructed by addition of a lithiated pyrone 5 to aldehyde 6.
M T, Crimmins, C A, Carroll, B W, King
openaire +2 more sources
Synthesis of the C1-C13 Fragment of (+)-Callipeltoside A
Synlett, 2007The synthesis of the C1-C13 fragment of (+)-callipeltoside A has been achieved in 12 steps with an overall yield of 11%.
Boulard, L. +3 more
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