Results 91 to 100 of about 90,564 (138)
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Alkylation of 1,2,5-Trisubstituted Pyrroles with Donor-Acceptor Cyclopropanes.

Journal of Organic Chemistry
Despite their inherently high nucleophilicity, pyrroles have rarely been explored in Friedel-Crafts-type alkylation reactions with donor-acceptor cyclopropanes (DACs).
Abhijit Gogoi   +3 more
semanticscholar   +1 more source

Copper-Catalyzed Asymmetric Nucleophilic Opening of 1,1,2,2-Tetrasubstituted Donor-Acceptor Cyclopropanes for the Synthesis of α-Tertiary Amines.

Journal of the American Chemical Society
Catalytic asymmetric transformation of donor-acceptor cyclopropanes (DACs) has been proven to be a highly valuable and robust strategy to construct diverse types of enantioenriched molecules.
Shouang Lan   +11 more
semanticscholar   +1 more source

A Synthetic Route to Functionalized Thiopyran Derivatives via Domino Ring-Opening Cyclization (DROC) of Donor-Acceptor Cyclopropanes with Pyridinium Thiolates.

Journal of Organic Chemistry
An efficient route to 5,6-dihydro-4H-thiopyran derivatives is developed via domino ring-opening cyclization (DROC) of activated donor-acceptor (DA)-cyclopropanes with pyridinium thiolates in the presence of Yb(OTf)3 as the Lewis acid and K2CO3 as the ...
Satysen Yadav   +4 more
semanticscholar   +1 more source

In(OTf)3-Catalyzed [3 + 2] Cycloaddition Reactions of Donor-Acceptor Cyclopropanes with Thioamides.

Journal of Organic Chemistry
An In(OTf)3-catalyzed [3 + 2] cycloaddition reaction between donor-acceptor cyclopropanes enabled by a single keto acceptor (cyclopropyl ketones) and thioamides has been developed.
Chen-Ying Zhai   +3 more
semanticscholar   +1 more source

Asymmetric Catalytic Reactions of Donor-Acceptor Cyclopropanes.

Angewandte Chemie, 2020
Due to the synergistic "push-pull" effect of vicinal electron-donating and electron-withdrawing groups, donor-acceptor (D-A) cyclopropanes have been recognized as one of the most powerful reagents to generate polyfunctional reactive intermediates after a
Yong Xia, Xiaohua Liu, Xiaoming Feng
semanticscholar   +1 more source

Stereoselective synthesis of functionalized perhydropyrrolo[1,2-b]isoxazoles based on (3 + 2)-annulation of donor-acceptor cyclopropanes and isoxazolines.

Organic and biomolecular chemistry
A stereoselective route to access substituted pyrrolidine cores via Lewis acid catalyzed (3 + 2)-annulation of donor-acceptor cyclopropanes (DACs) and isoxazolines has been developed.
K. V. Potapov   +7 more
semanticscholar   +1 more source

Organocatalytic Enantioselective Nitro-Vinylcyclopropane-Cyclopentene Rearrangement: Expanding the Reactivity of Donor–Acceptor Cyclopropanes

Synthesis
The catalytic enantioselective rearrangement of nitro-vinylcyclopropylacetaldehydes has been studied using chiral secondary amines as catalysts. The reaction proceeds through the in situ generation of a donor–acceptor cyclopropane, which rearranges to ...
Lorena García   +5 more
semanticscholar   +1 more source

Harnessing the Reactivity of Cyclopropenes in the Synthesis of Spiroketals via Putative Generation of Donor-Acceptor Cyclopropanes.

Organic Letters
TMSOTf-mediated 5/6-exo-trig hydroalkoxylation followed by the (3 + 2) cycloaddition cascade reaction of hydroxy cyclopropenes with aldehydes gave an expedient, stereoselective synthesis of [5.5]-and [6.5]-spiroketal derivatives.
Santosh J. Gharpure   +2 more
semanticscholar   +1 more source

DBU-Promoted (4 + 1) Annulation of Donor-Acceptor Cyclopropanes with 3-Phenylisoxazol-5(4H)-one: Access to Spiroisoxazol-5(4H)-one Derivatives.

Journal of Organic Chemistry
A DBU-promoted (4 + 1)-annulation reaction between donor-acceptor (D-A) cyclopropanes and 3-phenylisoxazolone has been developed. Using this method, some valuable spiroisoxazol-5(4H)-one derivatives can be obtained easily in good yields.
Wenzhe Cheng   +4 more
semanticscholar   +1 more source

Cu(OTf)2 Catalyzed the Reaction of Donor‐Acceptor Cyclopropanes With Salicylaldehyde Phenylhydrazones: Synthesis Polycyclic Tetrahydropyridazines

Journal of Heterocyclic Chemistry
A simple method has been developed to prepare tetrahydro‐5H‐chromeno[4,3‐c]pyridazin‐5‐ones by reacting donor‐acceptor cyclopropane 1,1‐dieters with salicylaldehyde phenylhydrazones in the presence of Cu(OTf)2, yielding moderate results with excellent ...
Zhipin Liu   +7 more
semanticscholar   +1 more source

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