Results 261 to 270 of about 149,811 (326)
Some of the next articles are maybe not open access.
ACS Catalysis, 2019
Herein, we describe an example of catalytic asymmetric synthesis of sulfinamides. Aromatic sulfenamides were chosen as useful substrates, because of the indispensable N–H bond, which could form an efficient hydrogen bond with chiral phosphoric acid. H2O2
LongJian Ma +5 more
semanticscholar +1 more source
Herein, we describe an example of catalytic asymmetric synthesis of sulfinamides. Aromatic sulfenamides were chosen as useful substrates, because of the indispensable N–H bond, which could form an efficient hydrogen bond with chiral phosphoric acid. H2O2
LongJian Ma +5 more
semanticscholar +1 more source
Journal of the American Chemical Society, 2019
The Pictet-Spengler (PS) reaction, i.e., the acid-catalyzed condensation between β-arylethylamine and an aldehyde or a ketone and the subsequent ring closure, is an important reaction in organic chemistry. A number of enzymes (called Pictet-Spenglerases,
X. Sheng, F. Himo
semanticscholar +1 more source
The Pictet-Spengler (PS) reaction, i.e., the acid-catalyzed condensation between β-arylethylamine and an aldehyde or a ketone and the subsequent ring closure, is an important reaction in organic chemistry. A number of enzymes (called Pictet-Spenglerases,
X. Sheng, F. Himo
semanticscholar +1 more source
Enantioselective polyene cyclizations
Organic & Biomolecular Chemistry, 2016A comprehensive review covering the field of enantioselective polyene cyclizations.
Chad N, Ungarean +2 more
openaire +2 more sources
International Journal of Mass Spectrometry, 2000
Abstract Determination of the intrinsic noncovalent interactions governing chiral recognition in diastereomeric complexes constitutes the basis for understanding information transfer between molecules in living systems as well as in synthetic supramolecular structures.
FILIPPI, Antonello +3 more
openaire +2 more sources
Abstract Determination of the intrinsic noncovalent interactions governing chiral recognition in diastereomeric complexes constitutes the basis for understanding information transfer between molecules in living systems as well as in synthetic supramolecular structures.
FILIPPI, Antonello +3 more
openaire +2 more sources
Enantioselective cooperative catalysis
Organic & Biomolecular Chemistry, 2015This review focuses on enantioselective cooperative catalytic reactions, wherein two catalysts work simultaneously to form products which cannot be obtained by the use of a single catalyst alone, which have attracted considerable attention in recent years.
Suleman M, Inamdar +2 more
openaire +2 more sources
Organocatalytic enantioselective desymmetrisation
Chem. Soc. Rev., 2016Organocatalytic enantioselective desymmetrisation of achiral or meso compounds is a powerful strategy for the construction of enantiomerically enriched complex molecules, often with multiple stereocentres and in high selectivities. Recent years have seen increasing use of organocatalysts in desymmetrisation methodology, in contrast to traditional metal-
A, Borissov +5 more
openaire +2 more sources
Catalytic Enantioselective Oxaziridination
Journal of the American Chemical Society, 2011The first catalytic enantioselective synthesis of oxaziridines is presented. The oxidation of aryl and alkyl aldimines with m-CPBA under organocatalytic conditions using cinchona alkaloid-derived catalysts furnished optically active oxaziridines in good yields and high enantioselectivities (up to 94% ee).
Lykke, Lennart +2 more
openaire +2 more sources
Enantioselective Radical Processes
ChemInform, 2003AbstractFor Abstract see ChemInform Abstract in Full Text.
Mukund P, Sibi +2 more
openaire +2 more sources
Enantioselective Halogenation Reactions
ChemInform, 2004AbstractFor Abstract see ChemInform Abstract in Full Text.
Hasim Ibrahim, Antonio Togni
openaire +1 more source
Enantioselective Phosphine Organocatalysis
Synlett, 2009The broad potential synthetic usefulness of phosphine-promoted reactions has stimulated many recent investigations on enantioselective variants of known reactions of this family, as well as the search for new, specifically designed, chiral phosphorus catalysts.
Marinetti, A., Voituriez, A.
openaire +1 more source

