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 ChemistryDespite 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
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
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
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
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 ChemistryAn 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, 2020Due 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
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
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
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
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
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
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
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
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
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
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

