Results 21 to 30 of about 360 (157)

Divergent Asymmetric Synthesis of Chiral Spiroheterocycles through Pd-Catalyzed Enantio- and Diastereoselective [3 + 2] Spiroannulation

open access: yes, 2022
The palladium-catalyzed divergent asymmetric synthesis of chiral spiro-furanindoline derivatives is described. The zwitterionic alkoxy π-allyl Pd(II) intermediate, generated catalytically from vinyl ethylene carbonate (VEC), could undergo ligand ...
Su Min Park (14248329)   +3 more
core   +1 more source

I2–PPh3 mediated spiroannulation of unsaturated b-dicarbonyl compounds. The first synthesis of (±)-negundoin A [PDF]

open access: yes, 2013
An efficient and stereoselective spiroannulation of unsaturated enols is reported. Unsaturated b-dicarbonyl compounds undergo cyclization by reaction with catalytic I2–PPh3, affording the corresponding spiro enol ether derivatives, with complete regio ...
Chahboun, Rachid   +6 more
core   +1 more source

Electrophilic functionalisation of indoles [PDF]

open access: yes, 2020
This Thesis describes efforts to develop improved methods to synthesise spirocyclic scaffolds based on indole through the development of a novel library of bis-electrophilic reagents.
Rossi-Ashton, James
core   +5 more sources

Diastereoselective spiroannulation of phenolic derivatives: Effect of steric hindrance on the diastereoselectivity. [PDF]

open access: yes, 2010
The objective of this study was to determine the effect, if any, that steric factors have on the oxidative spiroannulation of simple phenols bearing substituents that are increasing in size.

core   +1 more source

Gold(I)-Catalyzed Ring-Expanding Spiroannulation of Cyclopropenones with Enynes

open access: yes, 2016
The gold­(I)-catalyzed ring-expanding spiroannulation of cyclopropenones with enynes is reported here. A molecule of water is incorporated into the products during the spiroannulation to afford spirocyclic cyclopentenones containing an alcohol ...
Takanori Matsuda (1830835)   +1 more
core   +1 more source

Concise Synthesis of Spirocyclic Dihydrophthalazines through Spiroannulation Reactions of Aryl Azomethine Imines with Cyclic Diazo Compounds

open access: yes, 2022
Spiroannulation reactions are fundamental and invaluable for the synthesis of spirocyclic compounds. Presented herein are novel cascade reactions of aryl azomethine imines with cyclic diazo compounds leading to the formation of spirocyclic ...
Xinying Zhang (808783)   +4 more
core   +1 more source

Dearomatizing Spiroannulation Reagents: Direct Access to Spirocycles from Indoles and Dihalides [PDF]

open access: yesOrganic Letters, 2018
Unfunctionalized indoles can be directly converted into 3,3'-spirocyclic indolenines and indolines upon reaction with electrophilic dihalides in the presence of t-BuOK/BEt3. This double C-C bond forming reaction, which simultaneously generates a quaternary spirocyclic center, typically proceeds in high yield and has good functional group tolerance.
Liddon, John T R   +3 more
openaire   +4 more sources

Participation of β‑Ketothioamides in N‑Heterocyclic Carbene-Catalyzed [3 + 3] Spiroannulation: Asymmetric Synthesis of Functionalized Spiro-piperidinone Derivatives

open access: yes, 2018
An N-heterocyclic carbene-catalyzed asymmetric [3 + 3] spiroannulation of β-ketothioamide was successfully developed. β-Ketothioamides exhibit an unusual reactivity to undergo a previously challenging lactamization reaction, and the desired spiro ...
Jia-Lu Zhang (3860683)   +6 more
core   +2 more sources

One‐Pot Cascade Synthesis of Isoquinolinone‐Fused Quinoxalines Through Sequential Rh(III)/Pd(II) Catalysis

open access: yesAdvanced Synthesis &Catalysis, Volume 367, Issue 20, October 29, 2025.
A new one‐pot, dual catalytic strategy for the synthesis of polycyclic isoquinolinone‐fused quinoxalines from commercially available N‐(2‐acetamidophenyl)benzamides and 1,3‐diynes is reported. This transformation proceeds via Rh(III)/Pd(II)‐mediated sequential NH/CH activation/annulation. Detailed mechanistic studies elucidate the reaction pathway. A
Wei‐Jung Chiu   +3 more
wiley   +1 more source

Electrophilic aryl spiroannulation induced by diaryliodonium salts: efficient synthesis of [5,5]-spiro lactone-lactam scaffolds from α-cyanocarboxylates

open access: yesGreen Synthesis and Catalysis
Spirocyclic architectures represent one of the privileged three-dimensional scaffolds in pharmaceutical chemistry and drug discovery, while the new-skeletal synthesis of spiromolecules from simple starting materials remains a challenging task.
Zhiyuan Bao   +4 more
doaj   +1 more source

Home - About - Disclaimer - Privacy