Results 81 to 90 of about 2,792 (191)

Spectroscopic data from "Photochemical approaches to azetidines"

open access: yes
Raw data from the thesis entitled "Photochemical Approaches to Azetidines" Physical sciences::Chemistry::Organic chemistry Q Science::QD Chemistry::QD241 Organic ...
Dowden, James
core   +1 more source

Recent Developments in Stereoselective Reactions of Sulfoxonium Ylides

open access: yesMolecules
This review probes the recent developments in stereoselective reactions within the area of sulfoxonium ylide chemistry since the early 2000s. An abundance of research has been applied to sulfoxonium ylide chemistry since its emergence in the early 1960s.
Ciarán O’Shaughnessy   +2 more
doaj   +1 more source

Diastereospecific Synthesis of Enantiomerically Pure Polysubstituted Azetidines from 1,3-Amino Alcohols with Three Chiral Centers

open access: yes, 2016
Diastereospecific Synthesis of Enantiomerically Pure Polysubstituted Azetidines from 1,3-Amino Alcohols with Three Chiral ...
Bernardo Olano (3037740)   +4 more
core   +1 more source

Stereoselective Construction of Highly Functionalized Azetidines via a [2 + 2]-Cycloaddition

open access: yes, 2016
A facile stereoselective synthesis of highly functionalized azetidines from a novel [2 + 2]-cycloaddition of 2-aminomalonates to chalcones is reported.
Yang Ye (175530)   +2 more
core   +2 more sources

Sulfonyl azides in multicomponent and cascade strategies for synthesizing heterocycle and non-heterocyclic scaffolds

open access: yesResults in Chemistry
Sulfonyl azides have emerged as remarkably versatile reagents in contemporary synthetic chemistry, functioning both as azide-transfer agents and as precursors to N-sulfonylketenimines and nitrenes that enable a broad array of bond-forming events.
Yavar Ahmadi   +2 more
doaj   +1 more source

The renaissance of strained 1-azabicyclo[1.1.0]butanes as useful reagents for the synthesis of functionalized azetidines

open access: yes, 2020
Since their discovery in the late 1960s, 1-azabicyclo[1.1.0]butanes have demonstrated to be interesting precursors of azetidines, because of the peculiar reactivity of the C3-N bond that allows double functionalization in the 1,3 positions. In particular,
Andresini M., Luisi R., Degennaro L.
core   +1 more source

Synthesis of 1,4-Benzodiazepines via Intramolecular C–N Bond Coupling and Ring Opening of Azetidines

open access: yesMolecules
A facile and efficient synthesis of functionalized 1,4-benzodiazepine derivatives under mild conditions was developed. The CuI/N,N-dimethylglycine-catalyzed intramolecular cross-coupling reaction of 1-(2-bromobenzyl)azetidine-2-carboxamides proceeded ...
Xin-Ming Xu   +5 more
doaj   +1 more source

Organocatalytic Enantioselective Desymmetrization of meso-Aziridines and Prochiral Azetidines

open access: yes, 2016
Catalytic enantioselective desymmetrization of meso-aziridines and azetidines is a powerful strategy for rapid synthesis of chiral building blocks. This review summarizes the progress in the development of these reactions by organocatalysis.
Wang, Zhaobin   +5 more
core   +2 more sources

Ring Expansions of Activated Aziridines and Azetidines

open access: yes, 2015
Facile construction of small and normal-sized, or more precisely, four to seven-membered aza-heterocyclic ring systems is always a challenging yet rewarding task for the synthetic organic chemists. Fortunately, activated aziridines and azetidines provide
Navya Chauhan   +7 more
core   +1 more source

Employing carboxylic acids in aryne multicomponent coupling triggered by aziridines/azetidines

open access: yes, 2016
The transition-metal-free aryne multicomponent coupling (MCC) involving carboxylic acids initiated by aziridines/azetidines has been reported. The use of aziridines as nucleophiles afforded N-aryl β-amino alcohol derivatives and the application of ...
Thangaraj, Manikandan   +5 more
core   +1 more source

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