Results 21 to 30 of about 27,650 (311)

Diastereo-selectivity in diels–alder cycloadditions of erythrose benzylidene-acetal 1,3-Butadienes with maleimides [PDF]

open access: yes, 2012
Maleimides were combined with D-erythrose benzylidene-acetal 1,3-butadienes 1 and 2 to study the facial selectivity of the Diels-Alder cycloadditions. The selectivity was found to be from moderate to good.
Alves, M. José   +4 more
core   +1 more source

Additivity of Heats of Combustion, LCAO Resonance Energies, and Bond Orders of Conformal Sets of Conjugated Compounds [PDF]

open access: yes, 1965
The notion of "conformal sets" of aromatic and other conjugated compounds is introduced. To a good approximation, it is found that the sum of the heats of combustion of the compounds in one set equals the sum for the compounds in the other set.
Marcus, R. A.
core   +1 more source

Carcinogenicity of 1,3-Butadiene

open access: yesEnvironmental Health Perspectives, 1992
1,3-Butadiene, a high-production volume chemical used largely in the manufacture of synthetic rubber, is a multiple organ carcinogen in rats and mice. In inhalation studies conducted in mice by the National Toxicology Program, high rates of early lethal lymphomas occurring at exposure levels of 625 ppm or higher reduced the development and expression ...
R L, Melnick, C C, Shackelford, J, Huff
openaire   +3 more sources

Kinetics of Intramolecular Chemical Exchange by Initial Growth Rates of Spin Saturation Transfer Difference Experiments (SSTD NMR) [PDF]

open access: yes, 2015
We report here the Initial Growth Rates SSTD NMR method, as a new powerful tool to obtain the kinetic parameters of intramolecular chemical exchange in challenging small organic and organometallic ...
Angulo   +40 more
core   +1 more source

Reactivity differences between 2,4- and 2,5-disubstituted zirconacyclopentadienes: a highly selective and general approach to 2,4-disubstituted phospholes. [PDF]

open access: yes, 2013
International audienceMixtures of 2,4- and 2,5-disubstituted zirconacyclopentadienes were obtained by the reductive dimerisation of terminal alkynes using the Cp2ZrCl2/lanthanum system.
Bousrez, Guillaume   +6 more
core   +2 more sources

New Piperazine Derivatives Synthesized from Thio-Substituted Polyhalogeno-2-nitro-1,3-butadienes

open access: yesE-Journal of Chemistry, 2010
It is known that polyhalogeno-nitro-1,3-butadienes are important starting materials for the synthesis of polyfunctionalized bioactive heterocycles.
S. Goksin Aydinli, Cemil Ibis
doaj   +1 more source

Synthesis of pyrrolizines by intramolecular capture of 1,4-dipolar intermediates in reactions of enamines with dimethyl acetylenedicarboxylate [PDF]

open access: yes, 1981
Solvent polarity and reaction temperature strongly influence the reactions of dimethyl acetylenedicar-boxylate (DMAD) with 1-pyrrolidinyl enamines of acyclic and cyclic ketones. Whereas DMAD and 1-[1-phenyl-2-(phenylthio)ethenyl]pyrrolidine (3) give only
Harkema, S.   +5 more
core   +3 more sources

4-Bromo-2H-1,3-oxazine-2,6(3H)-dione

open access: yesActa Crystallographica Section E, 2009
The title compound, C4H2BrNO3, is one of a series of three substituted oxauracils prepared as precursors in the preparation of 1-aza-1,3-butadienes. Although each structure has identical potential for N—H...O intermolecular hydrogen bonds, each
Damon Parrish   +3 more
doaj   +1 more source

An Alkyne Diboration/6π-Electrocyclization Strategy for the Synthesis of Pyridine Boronic Acid Derivatives. [PDF]

open access: yes, 2016
A new and efficient synthesis of pyridine-based heteroaromatic boronic acid derivatives is reported through a novel diboration/6π-electrocyclization strategy.
Adams   +24 more
core   +2 more sources

The TTC Approach in Practice and its Impact on Risk Assessment and Risk Management in Food Safety. A Regulatory Toxicologist's Perspective

open access: yesCHIMIA, 2014
There are many substances in food and drinking water from different contamination sources for which only insufficient or no toxicity data exist.
Beat J. Brüschweiler
doaj   +1 more source

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