222 research outputs found
Bis(μ-diethylphosphido-κ2 P:P)bis[bis(2,4,6-trimethylphenyl)indium(III)]
The title compound, [In2(C9H11)4(C4H10P)2], contains a centrosymmetric In2P2 core with short intermolecular In—P bonds. This core has acute P—In—P and obtuse In—P—In bond angles compared with other [R
2InPR′2]2 analogues, due to the presence of the bulky aromatic substituents on the In atom and the non-sterically demanding ethyl substituents on the P atom
Purification of fish muscle myosin heavy chain and quantification of the specific polyribosome-bound polypeptide
Deoxyribonucleic acid-dependent ribonucleic acid polymerase activity in rat liver after protein restriction
Ethyl 6-methyl-4-[2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-3-yl]-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carboxylate
A new Biginelli compound, C18H25BN2O4S2, containing a boronate ester group was synthesized from a lithium bromide-catalysed reaction. The compound crystallizes with two independent molecules in the asymmetric unit that differ mainly in the conformation of the ester functionality. The crystal structure is stabilized by intermolecular N—H⋯O and N—H⋯S hydrogen bonds involving the 3,4-dihydropyrimidine-2(1H)-thione NH groups as donors and the carbonyl O and thiophene S atoms as acceptors
The first oxazoline adduct of Zn(acac)2: bis(acetylacetonato-κ2 O,O′)(2-phenyl-2-oxazoline-κN)zinc(II)
The title material, [Zn(C5H7O2)2(C9H9NO)], was synthesized by the treatment of bis(acetylacetonato)zinc(II) monohydrate with 2-phenyl-2-oxazoline. The Zn atom is coordinated by two chelating acetylacetonate groups and one oxazoline ligand in the apical position of a slightly distorted square-pyramidal metal–ligand geometry
One-pot Selective Formylation and Claisen Rearrangement on Calix[4]arenes
A versatile synthon with formyl and allyl groups at the upper rim of calix[4]arene has been synthesized in two steps. Selective formylation of 25,27-diallyloxy-26,28-dihydroxycalix[4]arene, along with the Claisen rearrangement of the allyl groups, was achieved by reaction with hexamethylenetetraamine (hexamine) in glacial acetic acid. A control reaction of the dipropyl analogue shows that the selective formylation takes place independently of the Claisen rearrangement. The crystal structure of the dimethylacetal derivative of 5,17-diformyl-11,23-diallylcalix[4]arene is reported
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