Results 281 to 290 of about 3,016,957 (322)
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Cannabis XXII. Synthesis of spiro-compounds

Tetrahedron Letters, 1981
Abstract O-methyl-cannabispirenone has been synthesized by two new methods applying spiroannelation on 5,7-dimethoxyindan-1-aldehyde. An alternative high yield synthesis of the latter has been elaborated.
Jiří Novák, Cornelis A. Salemink
openaire   +2 more sources

Spiro Bicyclic Guanidino Compounds from Pufferfish: Possible Biosynthetic Intermediates of Tetrodotoxin in Marine Environments.

Chemistry, 2018
Tetrodotoxin (TTX, 1) is a potent neurotoxin that is widely found in both terrestrial and marine animals; however, the biosynthetic pathway and genes for TTX have not yet been elucidated.
Nozomi Ueyama   +7 more
semanticscholar   +1 more source

The catalytic asymmetric synthesis of CF3-containing spiro-oxindole-pyrrolidine-pyrazolone compounds through squaramide-catalyzed 1,3-dipolar cycloaddition.

Organic and biomolecular chemistry, 2019
Pharmaceutically important compounds were synthesized through the organocatalytic 1,3-dipolar cycloaddition reaction. In the presence of a cinchonine-derived squaramide catalyst, the cycloaddition of N-2,2,2-trifluoroethylisatin ketimines with α,β ...
Cuie Wang   +11 more
semanticscholar   +1 more source

The Quinary Catalyst-Substrate Complex Induced Construction of Spiro-Bridged or Cagelike Polyheterocyclic Compounds via a Substrate-Controlled Cascade Process.

Organic Letters, 2019
The asymmetric organocatalytic cascade reaction of cyclic β-oxo aldehydes to 2-hydroxycinnamaldehydes is developed. The bifunctional tertiary amine-thiourea catalyst was used in a rationally designed multiple catalysis where the asymmetric iminium ...
Chen Wang   +4 more
semanticscholar   +1 more source

Ring strain energy in ether‐ and lactone‐containing spiro compounds

, 2015
Ring strain energies (RSEs) have been calculated for oxygen-containing spiro compounds using the group equivalent reaction (GER) formalism. The RSEs for all compounds studied were calculated from the energies of fully-optimized structures at the MP2 ...
Matthew K. Stedjan, J. D. Augspurger
semanticscholar   +1 more source

Organocatalytic Asymmetric Synthesis of Spiro-Bridged and Spiro-Fused Heterocyclic Compounds Containing Chromane, Indole, and Oxindole Moieties.

Organic Letters, 2018
Following the reactivity inversion strategy, two different two-step sequences were designed and successfully applied to the asymmetric synthesis of spiro-bridged and spiro-fused heterocyclic compounds, which combined chromane, indole, and oxindole, three
Zhi-Hao You   +3 more
semanticscholar   +1 more source

Phosphorus–nitrogen compounds. Part 42. The comparative syntheses of 2-cis-4-ansa(N/O) and spiro(N/O) cyclotetraphosphazene derivatives: spectroscopic and crystallographic characterization, antituberculosis and cytotoxic activity studies

New Journal of Chemistry, 2019
Syntheses, structural properties and biological activities of ferrocenyl ansa- and spiro-cyclotetraphosphazenes were investigated.
Arzu Binici   +10 more
semanticscholar   +1 more source

Synthesis of Tricyclic Spiro Compounds on the Basis of Alloocimene.

ChemInform, 2005
AbstractFor Abstract see ChemInform Abstract in Full Text.
M. S. Mitkova   +2 more
openaire   +3 more sources

Electronic properties of spiro compounds for organic electronics

The Journal of Chemical Physics, 2012
The electronic properties of p-type, n-type, and ambipolar spiro materials have been investigated using a combination of photoemission spectroscopy, electron energy-loss spectroscopy, and density functional based calculations. Our results provide insight into the occupied density of states as well as the electronic excitation spectra.
Torsten Hahn   +8 more
openaire   +3 more sources

Extension and revision of the nomenclature for spiro compounds [PDF]

open access: possiblePure and Applied Chemistry, 1999
Abstract Spiro ring systems have two or more rings linked by one common atom. Several different methods are used to name such systems. Rules A-41, A-43, B-10 and B-12 (Nomenclature of Organic Chemistry, 1979) describe the basics of how to name these compounds.
openaire   +1 more source

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