Results 141 to 150 of about 5,904 (191)

Nanoparticle‐Catalysed 1,3‐Dipolar Cycloadditions [PDF]

open access: yesEuropean Journal of Organic Chemistry, 2020
The 1,3-dipolar cycloadditions of azomethine-ylides and -imines, nitrones, nitrilimines, and azides catalysed by inorganic nanoparticles are described.
Giorgio Molteni, Alessandro Ponti
exaly   +3 more sources
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Stereoselective Photoredox Catalyzed (3+3) Dipolar Cycloaddition of Nitrone with Aryl Cyclopropane

Angewandte Chemie, 2023
AbstractBy resorting to the principle of remote activation, we herein demonstrate the first photoredox catalyzed (3+3) dipolar cycloaddition of nitrones with aryl cyclopropanes. Key to the fidelity of the reaction resides in a facile manner of substrate activation by single‐electron transfer (SET) oxidation with photoredox catalysis, and the reaction ...
Yao Xu   +6 more
openaire   +2 more sources

1,3-Dipolar cycloadditions of MeOPEG-bounded azides [PDF]

open access: yesTetrahedron, 2005
1,3-Dipolar cycloadditions of MeOPEG-supported azide 2 with a variety of dipolarophiles have been studied. 1-MeOPEGsupported 1,2,3-triazoles 4 and 5, 1,2,3,4-tetrazoles 12 and aziridine 14 were obtained in nearly quantitative yields. The removal of the
Giorgio Molteni, Paola Del Buttero
exaly   +2 more sources

Organocatalytic Enantioselective Dipolar [3+2] Cycloadditions of Acetylenic Aldehydes with Nitrones for the Formation of Chiral 4‐Isoxazolines [PDF]

open access: yesAdvanced Synthesis and Catalysis, 2012
The first organocatalytic enantioselective protocol has been developed for the dipolar [3+2]?cycloaddition between acetylenic aldehydes and nitrones through an iminium activation pathway.
, Xianrong Cai
exaly   +1 more source

New Parabanate Products by 1, 3-Dipolar Cycloaddition Reaction (‘Criss-Cross’ Cycloaddition)

High Performance Polymers, 1999
New parabanate products containing 1, 3, 5, 7-tetraazabicyclo[3, 3, 0]octane-2, 6-dione are described. The synthesis of αω-diisocyanato-telechelics starting from two diisocyanates having a preformed parabanic unit using a [3+2] dipolar cycloaddition reaction was studied.
Adrian A Caraculacu   +2 more
openaire   +1 more source

ChemInform Abstract: [2 + 3]Dipolar Cycloadditions of a Monomeric Thioaldehyde.

Chemischer Informationsdienst, 1986
AbstractThiopivalaldehyd (I) liefert mit den Nitronen (II) und (IV), dem Nitriloxid (VI), der Diazoverbindung (VIII) sowie dem Azomethinimin (X) die stabilen [2 + 3]‐Cycloaddukte (III), (V), (VII), (IX) und (XI).
E. VEDEJS, R. G. WILDE
openaire   +1 more source

Captodative Alkenes in Concerted 1, 3-Dipolar Cycloadditions

1986
The 1, 3-dipolar cycloaddition of an E-/Z-pair of captodative alkenes to a cyclic aldonitrone is demonstrated to occur stereospecifically. Additions of α-(tert-butylthio)acrylonitri le to a series of C, N-diphenylnitrones show a change in regioselectivity upon donor substitution in the C-phenyl-ring.
Dietrich Döpp   +2 more
openaire   +1 more source

Trimethylsilyl Triflate-promoted [2+3] Dipolar Cycloaddition of Nitrones with Allyltrimethylsilane

HETEROCYCLES, 1992
3-Alkyl-5-trimethylsilylmethylisoxazolidines are accessible in good yields and at temperatures ≤ 20°C, by the trimethylsilyl triflate-promoted reaction of allyltrimethylsilane with aliphatic nitrones.
Claudio Trombini, Dilip D. Dhavale
openaire   +1 more source

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