Results 161 to 170 of about 2,677,083 (277)

Enantioselective Conjugate Addition of Malononitriles to Enynes: A Stereodivergent Approach to Chiral Allenes

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Quinine‐catalyzed enantioselective conjugate addition of malononitrile derivatives to enynes provides trisubstituted chiral allenes in good to excellent yields and high enantiopurities under mild conditions. Broad substrate scope, easy scalability, and versatile post‐synthetic transformations into enantioenriched pyrazoles and furans highlight the ...
Martin Kamlar   +3 more
wiley   +1 more source

Nucleophilic Reactions of Cyclobutenones and the Related 4,4‐Dichlorocyclobutenone Derivatives

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Cyclobutenone derivates and their 4,4‐dichloro counterparts have an uninterrupted attention as useful synthons in the synthesis of complex organic molecules. Their nucleophilic reactions remain underexplored. This review brings attention to these reactions, whose outcome is not straightforward.
Sarah J. Wright   +2 more
wiley   +1 more source

Emergent Atropisomerism Through Diels–Alder Reactions of Vinylallenes

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Cycloaddition‐induced geometric reorganization transforms achiral vinylallenes into atropisomeric styrenes. Conformational flexibility governs atropisomerization barriers, thermodynamic preferences, and configurational stability. Atropisomeric styrenes remain comparatively underdeveloped because configurational stability about the C(sp2)C(sp2) bond is
Kusum Sai   +3 more
wiley   +1 more source

Investigation of α‐Silylalcohols as Chiral Umpolung Carbanion Surrogates Through Stereospecific 1,2‐Brook Rearrangement

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Deprotonation of chiral α‐silyl secondary alcohols leads to masked polarity‐reversed chiral carbanions through stereospecific 1,2‐Brook rearrangement. In situ trapping with Weinreb amide electrophiles affords α‐hydroxyketones with moderate to excellent enantiospecificity (es).
TyAnn McHenry, Joshua D. Sieber
wiley   +1 more source

Bromonitroalkanes in Organic Synthesis

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
α,α‐Bromonitroalkanes (BNAs) exhibit chameleon‐like reactivity, serving as carbene, radical, carbanion, and carbocation synthons. This mini‐review summarizes the different reaction modes and highlights recent developments in thermal and photochemical processes. α,α‐Bromonitroalkanes (BNAs) exhibit chameleon‐like reactivity, serving as carbene, radical,
Magdalena Koch, Oliver Reiser
wiley   +1 more source

Copper-Catalyzed Enantioselective Synthesis of Chiral Selenium-Based Versatile Synthons. [PDF]

open access: yesACS Cent Sci
Huang Q   +6 more
europepmc   +1 more source

Axial Chirality Control Through Palladium‐Catalyzed Alkenylation Reactions for the Atroposelective Synthesis of 4‐Arylquinolin‐2‐ones

open access: yesEuropean Journal of Organic Chemistry, EarlyView.
Palladium(II)‐catalyzed intramolecular C─H alkenylation of cinnamides allows the atroposelective synthesis of axially chiral 4‐arylquinolones, with the chirality being installed by ring formation. DFT studies have shown that the reaction proceeds by prior activation of the alkene and the enantioselectivity is determined during the β‐hydride elimination
Brenda Fundora   +8 more
wiley   +1 more source

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