Results 91 to 100 of about 8,858 (221)
Progress of Enantioselective Nitrile Biotransformations in Organic Synthesis
Recent progress of enantioselective biotransformations of nitriles including various functionalized nitriles, ?-hydroxy and ?-amino nitriles, oxirane- and aziridine-containing carbonitriles is summarized in this short review article.
Mei-Xiang Wang
doaj +1 more source
Aziridine−Allylsilane-Mediated Total Synthesis of (−)-Yohimbane
A total asymmetric synthesis of (−)-yohimbane and ent-alloyohimbane is reported. The synthesis utilizes a novel aziridine−allylsilane cyclization reaction as a key step in the synthesis.
Punit P. Seth (628027) +1 more
core +1 more source
The utility of aziridine as a clickable moiety for post-modification of polydimethylsiloxane is demonstrated.
Hyun Kyung Moon +2 more
core +1 more source
Jaunu C-C saišu veidošana aziridīn-2-karbonskābes atvasinājumos, saglabājot trīslocekļu slāpekļa heterociklus. Štrumfs B., zinātniskais vadītājs Dr. ķīm. Trapencieris P. Promocijas darbs, 165 lappuses, 6 attēli, 3 tabulas, 100 literatūras avoti. Latviešu
Štrumfs, Boriss, Boriss Štrumfs
core
Efficient, regioselective ring-opening of activated aziridine-2-carboxylates with [18F]fluoride
Aziridines can undergo a range of ring-opening reactions with nucleophiles. The regio- and stereochemistry of the products depend on the substituents on the aziridine. Aziridine ring-opening reactions have rarely been used in radiosynthesis.
Hansen, Paul Robert +3 more
core +1 more source
Small Nitrogen Heterocycles Containing 1,2,3-Triazoles in the Side Chain
New libraries of aziridine and azetidine derivatives containing 1,4-disubstituted 1,2,3-triazole in the side chain as well as aziridine derivatives containing 1,5-disubstituted 1,2,3-triazole in the side chain were synthesized by transition metals ...
Suta, Krista +2 more
core
Studies on Substituted Aziridine-Boranes
2-Methylaziridine—borane, 1,2-dimethylaziridine-borane, 2,2-dimethylaziridine-borane, N-ethylaziridine-borane, 2-ethyl- aziridine-borane, and 2~phenylaziridine-borane have been prepared for the first time.
Lee, Jae
core
Secondary 3‐Chloropiperidines: Powerful Alkylating Agents
In previous works, we demonstrated that tertiary 3‐chloropiperidines are potent chemotherapeutics, alkylating the DNA through the formation of bicyclic aziridinium ions. Herein, we report the synthesis of novel secondary 3‐chloropiperidine analogues. The
Mats Georg +5 more
doaj +1 more source
A Facile Synthesis of Amino Acid Derivatives from Aziridines in Liquid Sulfur Dioxide
In the past decades aziridines have played a role of versatile intermediates and important precursors for the synthesis of nitrogencontaining biologically active compounds. Modification of aziridine cycle leads to formation of agents of different classes,
Lugiņina, Jevgeņija, Turks, Māris
core
Glycosyl Aziridine Carbamates as Versatile Donors for Catalytically Activated Glycosylation
Catalytically promoted glycosylation continues to pose challenges in carbohydrate synthesis, as glycosyl donors that tolerate multistep manipulations often require stoichiometric activation, whereas donors amenable to catalytic activation can exhibit ...
Meifang Yang +13 more
core +2 more sources

