Results 241 to 250 of about 63,493 (303)

<i>N</i>-Phenyl-[1,1'-biphen-yl]-2-carboxamide. [PDF]

open access: yesIUCrdata
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]

open access: yesActa Crystallogr E Crystallogr Commun
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]

open access: yesActa Crystallogr E Crystallogr Commun
Shishkina SV   +5 more
europepmc   +1 more source

Diterpenoids. XXXIV. The C13 configuration of tetrahydroabienol

open access: yesAustralian Journal of Chemistry, 1976
Tetrahydroabienol is a quasiracemic compound formed from C13 epimers.
Carman R.M., Zerner G.W.
core   +5 more sources
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The Concentration of C13

The Journal of Chemical Physics, 1940
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]

open access: yesBiochimica Et Biophysica Acta - Molecular Cell Research, 1998
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

open access: yes, 1995
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, 2007
The 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
openaire   +2 more sources

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