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Catalytic Strategies for Amide‐Based Michael Additions: Advances and Perspectives

open access: yesJournal of Chemistry, Volume 2026, Issue 1, 2026.
The Michael addition is a cornerstone transformation in organic synthesis, enabling efficient C–C and C–heteroatom bond formation. Traditionally, α,β‐unsaturated carbonyl compounds such as enones and esters have dominated as Michael acceptors, whereas α,β‐unsaturated amides remain underutilized due to their strong resonance stabilization and low ...
Muhammad Naufal   +6 more
wiley   +1 more source

Diastereoselective Reformatsky Reaction Mediated by Dichlorocyclopentadienyltitanium(III). [PDF]

open access: yesMolecules
López-Martínez JL   +4 more
europepmc   +1 more source

Modeling ring-chain-ring tautomerization of N-(o-aryl)-4-hydroxy-2-oxazolidinone derivatives [PDF]

open access: yes, 2011
Aviyente, V   +5 more
core  

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