Results 131 to 140 of about 29,810 (265)
Spectroscopy and Conformer‐Selective Photoelectron Circular Dichroism of Chiral Molecules
Photoelectron circular dichroism (PECD) is a forward–backward asymmetry in the angular distribution of the electrons emitted by a chiral molecule ionized by a circularly polarized light (CPL). Its sensitivity to conformation is studied by one‐photon or resonance‐enhanced two‐photon ionization, the latter being conformer‐selective.
Laurent Nahon, Anne Zehnacker
wiley +1 more source
Stereoselective cyclo-addition reactions of azomethine ylides catalysed by in situ generated Ag(I)/bisphosphine complexes [PDF]
Stereoselective cyclo-addition reactions of azomethine ylides promoted by in situ generated Ag(I)/bisphosphine complexes were studied. Under the optimised conditions, the pyrrolidine products were isolated in up to 84 % yield and with up to 71 % e.e. The
RONALD GRIGG +2 more
core
Insert text for Table of Contents here. In this research, the synthesis of new Cyrene derivatives (Cyrene dimethyl acetal and Cyrene diethyl acetal) was accomplished, and the investigation of their physicochemical properties was completed. It was also shown after a detailed optimization study that Cyrene dimethyl acetal could be an appropriate ...
Attila Takács +6 more
wiley +1 more source
Carbohydrate‐Based Drug Discovery: Synthetic Strategies and Clinical Applications
The picture depicts the molecules discussed in the review. On the left side, the general scaffold of sugars is shown. Next to it are four carbohydrate‐based molecules, including remdesivir, islatravir, empagliflozin, and Globo‐H. Remdesivir and islatravir contain a substituted ribose ring attached to a modified nucleobase.
Stephan Scheeff +2 more
wiley +1 more source
Treatment of N,N-dimethylhydrazinoalkenes with diethylzinc followed by exposure of the resulting ethylzinc amides to high vacuum drives a Schlenck redistribution metalloamination/cyclization to generate the corresponding bis(organozinc) intermediates in ...
Jérome Lépeule +2 more
doaj +1 more source
Recent theoretical efforts to elucidate the origin of enantioselectivity in transition metal‐catalyzed propargylic substitution reactions are highlighted in this review. ABSTRACT In recent years, asymmetric catalytic propargylic substitution reactions have undergone remarkable development, enabling the construction of chiral carbon centers adjacent to ...
Ken Sakata, Yoshiaki Nishibayashi
wiley +1 more source
Synthesis of a Carbon‐Linked Acyldepsipeptide Derivative
The synthesis of a methylene‐linked acyldepsipeptide (ADEP) is reported. Success relied upon an improve method to generate a versatile vinyl glycine methyl ester synthon and a rationally optimized Grubb’s metathesis. NMR and in silico studies revealed an unusual trans–trans proline orientation for this new unnatural ADEP analog, advancing the ...
Katelyn G. Stevens-Davis +6 more
wiley +1 more source
Piperidines from acid-catalysed cyclisations: Pitfalls, solutions and a new ring contraction to pyrrolidines [PDF]
Aldmairi, Abdu H. +4 more
core +2 more sources
Alkylidenecyclopropanes (ACPs) can work as versatile 3 C partners in a range of [3+n] cycloadditions with unsaturated carbon partners. We now demonstrate that they can also be harnessed for inter‐ and intramolecular palladium‐catalyzed [3+2] formal ...
Ricardo Rodiño +3 more
doaj +1 more source
A combined experimental and theoretical investigation of the stereoselectivity in the synthesis of azahetrocyclic phosphonates [PDF]
Since the discovery of the biological activity of aminoalkylphosphonates, e.g. as enzyme inhibitors, many researchers have focused their attention on conformationally constrained azaheterocyclic phosphonates. Stereocontrol is of major interest during the
Claeys, Diederica +5 more
core +1 more source

