Results 161 to 170 of about 26,606 (255)

Alkoxyallenes in Modern Synthesis: Reactivity, Catalysis, and Complexity Generation

open access: yesAdvanced Synthesis &Catalysis, Volume 368, Issue 17, 1 September 2026.
The last decade has witnessed a remarkable transformation in alkoxyallene chemistry. Although historically employed as synthetic equivalents of acrolein or as versatile 3C synthons, alkoxyallenes are now increasingly recognized as highly adaptable platforms for synthetic design.
A. Lanfranco   +5 more
wiley   +1 more source

Highly Cα-regio-, enantio- and diastereoselective Mukaiyama-type annulation of siloxyfurans: stereodivergent synthesis of multi-stereogenic tricyclic γ-lactones. [PDF]

open access: yesChem Sci
Gan L   +14 more
europepmc   +1 more source

Transition Metal‐Free Vinylcyclopropanation of Olefins via Carbolithiation Reactions: Synthesis of 3‐Azabicyclo[3.1.0]hexanes

open access: yesAdvanced Synthesis &Catalysis, Volume 368, Issue 17, 1 September 2026.
Readily accessible N‐allyl‐N‐2‐bromoallylamines undergo a tandem lithiation–cyclization cascade to furnish highly substituted 3‐azabicyclo[3.1.0]hexanes. The transformation proceeds without transition metals and delivers products with excellent diastereocontrol across a broad substrate range.
Nuria Cases   +5 more
wiley   +1 more source

Asymmetric Deoxy-Fluoroalkylation of Amides Enabled by Transimination. [PDF]

open access: yesOrg Lett
Wilt JA   +7 more
europepmc   +1 more source

Cobalt/Photoredox Catalyzed Desymmetrization of Oxo and Azabicycles via Asymmetric Reductive Coupling With Alkynes

open access: yesAdvanced Science, Volume 13, Issue 52, 18 September 2026.
A one‐step, asymmetric reductive coupling of alkynes and oxa‐ and aza‐bicyclic olefins using a cobalt/photoredox catalytic system through desymmetrization. ABSTRACT Bicyclo[2.2.1]heptane frameworks represent a privileged structural motif prevalent in numerous natural products and bioactive molecules.
Subhankar Pradhan   +5 more
wiley   +1 more source

Asymmetric Total Synthesis of (-)-Verrucarol. [PDF]

open access: yesAngew Chem Int Ed Engl
Powers MH   +5 more
europepmc   +1 more source

Overview of Photochemical Reactions for the Synthesis of Aza and Oxa‐Spirocyclic Compounds Under Visible Light Irradiation

open access: yesChemistry &Biodiversity, Volume 23, Issue 9, September 2026.
This review presents the visible‐light‐mediated photochemical reaction for the synthesis of aza, oxa, and aza–oxa spirocyclic compounds via photoinduced electron transfer (PET), hydrogen atom transfer (HAT), single‐electron transfer (SET), or energy transfer (EnT) pathways.
Annu Bhardwaj   +4 more
wiley   +1 more source

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