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Visible-Light-Driven Unsymmetric gem-Difunctionalization of Vinyl Azides with Thiosulfonates or Selenosulfonates.

Organic Letters
Thiosulfonylation and selenosulfonylation of vinyl azides with thiosulfonates and selenosulfonates were achieved using Cu(dap)2Cl as a photosensitizer under visible-light irradiation. This reaction is the application of a vinyl azide substrate in a group
Tao Wang   +5 more
semanticscholar   +1 more source

Isomerisation of Vinyl Sulfones for the Stereoselective Synthesis of Vinyl Azides

European Journal of Organic Chemistry, 2020
Reported is the construction, and facile base‐mediated conversation of ten differently substituted 3‐azido E‐vinyl sulfones (γ‐azido‐α,β‐unsaturated sulfones) into their isomeric vinyl azide counterparts. The requisite 3‐azido E‐vinyl sulfones were prepared from 3‐bromo E‐vinyl sulfones, which in turn were accessed from allyl sulfones via a bromination‐
Collins, Niall   +3 more
openaire   +3 more sources

Modular Synthesis of Azidobicyclo[2.1.1]hexanes via (3 + 2) Annulation of α-Substituted Vinyl Azides and Bicyclo[1.1.0]butanes.

Journal of Organic Chemistry
Here, we present a mild and rapid method to access azidobicyclo[2.1.1]hexanes via formal (3 + 2) cycloaddition of α-substituted vinyl azides and bicyclo[1.1.0]butanes under Lewis acid catalysis.
Sai Hu   +4 more
semanticscholar   +1 more source

CuCl2·2H2O/TBHP mediated synthesis of β-enaminones via coupling reaction of vinyl azides with aldehydes.

Organic and biomolecular chemistry, 2022
A facile and efficient oxidative functionalization of vinyl azides with aldehydes furnishing a diverse array of β-acylated enaminones was developed.
Yaohong Zhang   +7 more
semanticscholar   +1 more source

Visible-Light-Triggered Synthesis of N-α-Ketoacylated Sulfoximines by Denitrogenative and Oxidative Functionalization of Vinyl Azides.

Journal of Organic Chemistry
We have introduced a sulfoximidation reaction initiated by visible light between α-phenyl vinyl azides and NH-sulfoximines. The cost-effective and readily accessible hypervalent iodine reagent (PIDA) easily promoted the oxidative sulfoximidation process ...
Subhankar Sarkar   +4 more
semanticscholar   +1 more source

S-Triggered Schmidt-type Rearrangement of Vinyl Azides to Access N-Aryl-(trifluoromethylsulfinyl)acetamides

Organic Chemistry Frontiers, 2022
A novel S-induced Schmidt-type rearrangement of vinyl azides with CF3SO2Na is reported, which is mediated by triphosgene (BTC) under mild reaction conditions.
Zhenhua Liu   +7 more
semanticscholar   +1 more source

Synthesis of Highly Substituted 2-Aminopyridines with Vinyl Azides, Isonitriles and Ketones.

Chemistry - An Asian Journal, 2022
We developed a facile, efficient method for synthesizing highly substituted 2-aminopyridines from unstable vinyl carbodiimides generated in situ in a one-pot transformation.
Wenxu Chang   +7 more
semanticscholar   +1 more source

Oxyphosphorodithiolation of Vinyl Azides with P4S10 and Alcohols Leading to β-Keto Phosphorodithioates.

Journal of Organic Chemistry
A simple strategy for the synthesis of β-keto phosphorodithioates has been developed through the direct oxyphosphorodithiolation of vinyl azides with P4S10 and alcohols in the presence of water.
Jian Huang   +7 more
semanticscholar   +1 more source

ChemInform Abstract: VINYL AZIDES AS DIAZOENAMINES

Chemischer Informationsdienst, 1973
AbstractIn Abhängigkeit von der Struktur reagieren Vinylazide mit NOBF4 zu l,2,5‐ und 1,2,4‐Oxadiazolen.
A. N. THAKORE   +2 more
openaire   +1 more source

[3 + 2] Annulation of Vinyl Azides with Aldehydes for the Synthesis of 3-Oxazolines via the [CO + CCN] Strategy.

Organic Letters
Despite the widespread utilizable value of 3-oxazolines, mild and efficient access to such a class of unique structures still remains, to date, a challenge. Herein, we present a [3 + 2] annulation strategy, guided by the retrosynthetic principle of [CO +
Chun-Mei Luo   +9 more
semanticscholar   +1 more source

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