Results 41 to 50 of about 6,575 (208)

Rhodium(III)-Catalyzed C-C Coupling between Arenes and Aziridines by C-H Activation

open access: yes, 2013
Rhodium(III)-Catalyzed C-C Coupling between Arenes and Aziridines by C-H ...
Wan, Boshun   +6 more
core   +1 more source

The synthesis and reactivity of N-diphenylphosphinyl aziridines

open access: yes, 1994
The synthesis of enantiopure N-diphenylphosphinyl (Dpp) protected aziridines from 2-aminoalcohols and the reactions of these aziridines with a range of nucleophiles is ...
Howson, Bill   +2 more
core   +5 more sources

Synthesis of 2-amino-3-arylpropan-1-ols and 1-(2,3-diaminopropyl)-1,2,3-triazoles and evaluation of their antimalarial activity

open access: yesBeilstein Journal of Organic Chemistry, 2011
A variety of 2-amino-3-arylpropan-1-ols, anti-2-amino-3-aryl-3-methoxypropan-1-ols and anti-2-amino-1-arylpropan-1,3-diols were prepared selectively through elaboration of trans-4-aryl-3-chloro-β-lactams.
Matthias D’hooghe   +9 more
doaj   +1 more source

Deprotection of Sulfonyl Aziridines

open access: yes, 2016
The deprotection of the chiral N-sulfonyl aziridines 1−3 has been studied under different desulfonylation conditions. Two methods for the efficient deprotection of 2-benzyl-, 2-phenyl-, and 2-carboxyl-N-sulfonylaziridines were found.
Diego A. Alonso (2145664)   +1 more
core   +1 more source

Synthesis of α-Aminophosphonic Acid Derivatives Through the Addition of O- and S-Nucleophiles to 2H-Azirines and Their Antiproliferative Effect on A549 Human Lung Adenocarcinoma Cells

open access: yesMolecules, 2020
This work reports a straightforward regioselective synthetic methodology to prepare α-aminophosphine oxides and phosphonates through the addition of oxygen and sulfur nucleophiles to the C–N double bond of 2H-azirine derivatives. Determined by the nature
Victor Carramiñana   +3 more
doaj   +1 more source

Intermolecular 3+3 Ring Expansion of Aziridines to Dehydropiperidines through the Intermediacy of Aziridinium Ylides [PDF]

open access: yes, 2019
Bicyclic aziridines undergo formal [3+3] ring expansion reactions when exposed to rhodium-bound vinyl carbenes to form complex dehydropiperidines in a highly stereocontrolled rearrangement.
Jennifer, Schomaker   +6 more
core   +1 more source

Borylcyclopropanes: Synthetic Strategies and Applications

open access: yesAngewandte Chemie, Volume 138, Issue 37, 7 September 2026.
Borylcyclopropanes (cyclopropanes bearing a boron substituent) sit at the intersection of two privileged frameworks in synthesis. This review provides the first exhaustive survey of their chemistry, spanning metal–carbene, nucleophilic cyclization, radical, hydroboration, and C─H activation routes, and documenting applications in medicinal chemistry ...
Aiza A. Butt, Joseph M. Ready
wiley   +2 more sources

Substituted Aziridines by Lithiation−Electrophile Trapping of Terminal Aziridines

open access: yes, 2016
Regio- and stereoselective deprotonation of N-Bus (Bus = tert-butylsulfonyl)-protected terminal aziridines with lithium 2,2,6,6-tetramethylpiperidide generates a nonstabilized (H-substituted) aziridinyl anion that undergoes in situ or external ...
David M. Hodgson (692207)   +2 more
core   +1 more source

Synthesis and Evaluation of Biological Activities of Aziridine Derivatives of Urea and Thiourea

open access: yesMolecules, 2017
In the present paper, we report the synthesis and evaluation of in vitro antimicrobial activities of aziridine-thiourea derivatives. A series of aziridines in reaction with isocyanates and isothiocyanates to obtain urea and thiourea derivatives were used.
Aleksandra Kowalczyk   +4 more
doaj   +1 more source

Formation of Scalemic Aziridines via the Nucleophilic Opening of Aziridines

open access: yes, 2016
Formation of Scalemic Aziridines via the Nucleophilic Opening of ...
Punit P. Seth (628027)   +1 more
core   +1 more source

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