Results 141 to 150 of about 3,335 (198)
The Chemistry of Selenosilanes: A Topic Overview. [PDF]
MoleculesTanini D, Capperucci A.
europepmc +1 more source
Chiral Monoamidines as Effective Organocatalysts for the Stereoselective Synthesis of Oxindoles under Homogeneous and Heterogeneous Conditions. [PDF]
J Org ChemToldo S +5 more
europepmc +1 more source
Highly Enantioselective Reduction of α-Methylated Nitroalkenes
Angewandte Chemie - International Edition, 2013 Burda E, Reß T, Winkler T, et al. Highly Enantioselective Reduction of α-Methylated Nitroalkenes. Angewandte Chemie (International ed. in English). 2013;52(35):9323-9326.Highly selective: The reduction of α-methyl-substituted nitroalkenes succeeds in a ...
Harald Gröger +2 more
exaly +2 more sources
Conjugate Addition of Indoles to Nitroalkenes Promoted by Basic Alumina in Solventless Conditions
Advanced Synthesis and Catalysis, 2006 Basic alumina is found to promote the conjugate addition of indoles to nitroalkenes in solventless conditions at 60° C. Nitroalkenes can be replaced by nitro alcohols that are converted into nitroolefins under the reaction conditions.
Alessandro Palmieri +2 more
exaly +3 more sources
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Organocatalytic Asymmetric Cyanosilylation of Nitroalkenes
Chemistry - A European Journal, 20105 páginas, 1 figura, 5 ...
Rosario Fernández +1 more
exaly +4 more sources
Organocatalytic Asymmetric Hydrophosphination of Nitroalkenes.
ChemInform, 2007AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
BARTOLI, GIUSEPPE +6 more
openaire +2 more sources
Catalytic enantioselective epoxidation of nitroalkenes
Chemical Communications, 2016Nitroepoxides are potentially exploitable as synthons with vicinal electrophilic centers.
Vidal-Albalat, Andreu +5 more
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Evaluation of Nitroalkenes as Nitric Oxide Donors
Bioorganic and Medicinal Chemistry Letters, 2007Chemiluminescence experiments demonstrate that simple nitroalkenes release low levels of nitric oxide. UV and EPR measurements suggest but cannot confirm direct NO release from nitroalkenes. Given the biological activity of nitrated unsaturated fatty acids, these results suggest the possible metabolic conversion of nitroalkenes to NO.
Bruce King, Jinming Huang
exaly +3 more sources
The addition of ethylenedinitrodiamine to nitroalkenes
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 19621. For the first time it was shown possible to add N-nitroamines to nitroalkenes, using the addition of ethylenedinitrodiamine to 1-nitrobutene-1 and 1-nitropentene-1 as an example, resulting In the formation of tetranitrodiazalkanes.
I. S. Ivanova (Korsakova) +2 more
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Catalytic Asymmetric β-Peroxidation of Nitroalkenes
Advanced Synthesis and Catalysis, 2008AbstractThe first example of an asymmetric β‐peroxidation of nitroalkenes is disclosed. The reaction is promoted by catalytic loadings of a commercially available diaryl‐2‐pyrrolidinemethanol derivative and tert‐butyl hydroperoxide as the oxidant. A synthetically useful class of peroxides is obtained in good yield and enantioselectivity (up to 84% ee).
Alessandra Lattanzi, Alessio Russo
exaly +2 more sources