Results 31 to 40 of about 337 (160)

EPR Evidence for the Origin of Nonlinear Effects in an Enantioselective Cu(II)-Catalyzed Spiroannulation

open access: yes, 2019
Herein, we describe an enantioselective Cu­(II)-catalyzed spiroannulation of N-Boc-iminooxindoles with allylsilanes where a significant positive nonlinear effect (NLE) is observed.
Troy A. Stich (1332660)   +5 more
core   +1 more source

DMAP-Catalyzed [4+3] Spiroannulation of Pyrazolone-Derived Morita–Baylis–Hillman Carbonates with N‑(o‑Chloromethyl)aryl Amides to Forge Spiro[pyrazolone-azepine] Scaffolds

open access: yes, 2023
A novel DMAP-catalyzed [4+3] spiroannulation of pyrazolone-derived Morita–Baylis–Hillman carbonates with N-(o-chloromethyl)aryl amides was developed.
Baomin Wang   +9 more
core   +1 more source

Synthesis of 3-spiroannulated hexahydro-6,8a-epoxyisoquinolines

open access: yesMendeleev Communications, 2002
The title compounds were synthesised by the intramolecular [4+2]-cycloaddition of 1-N-furfurylamino-1-allylcyclanes in the presence of acetic anhydride.
Varlamov A.V.   +4 more
openaire   +3 more sources

From Conventional to Sustainable Catalytic Approaches for Heterocycles Synthesis

open access: yesChemSusChem, Volume 17, Issue 8, April 22, 2024.
Catalysed synthetic methods, such as transition metals, organocatalysts, photocatalysts, iodine‐catalysed reaction, electrochemical reactions and green innovative methods are of great interest for the sustainable synthesis of heterocyclic compounds, important building blocks for several applications.
Carla Rizzo   +4 more
wiley   +1 more source

α,β-Unsaturated Acyl Cyanides as New Bis-Electrophiles for Enantioselective Organocatalyzed Formal [3+3]Spiroannulation

open access: yes, 2014
International audienceα,β-Unsaturated acyl cyanides are key bis-electrophile substrates for successful domino enantioselective organocatalyzed Michael-intramolecular acylation domino sequences.
Constantieux, Thierry   +4 more
core   +1 more source

Aniline Derivatives from Lignin under Mild Conditions Enabled by Electrochemistry

open access: yesChemSusChem, Volume 17, Issue 3, February 8, 2024.
Electrochemical oxidation of lignin‐derived guaiacols & syringols leads to cyclohexadienone intermediates in moderate to good yields. These react with ethyl glycinate hydrochloride under mild conditions to afford lignin‐based anilines. This methodology can be incorporated to reductive catalytic fractionation processes towards selective obtention of 4 ...
Antonio A. Castillo‐Garcia   +3 more
wiley   +1 more source

Rh(III)-Catalyzed Spiroannulation Reaction of N‑Aryl Nitrones with 2‑Diazo-1,3-indandiones: Synthesis of Spirocyclic Indole‑N‑oxides and Their 1,3-Dipolar Cycloaddition with Maleimides

open access: yes, 2023
An efficient strategy for the preparation of spirocyclic indole-N-oxide compounds through a Rh(III)-catalyzed [4 + 1] spiroannulation reaction of N-aryl nitrones with 2-diazo-1,3-indandiones as C1 synthons under extremely mild conditions is presented ...
Zhaotong Wei (14761249)   +4 more
core   +1 more source

Cp*Co(III)-Catalyzed Dearomative [3 + 2] Spiroannulation of 2‑Alkenylphenols with Ynamides via C–H Activation

open access: yes, 2019
An oxidative [3 + 2] C–H spiroannulation reaction of 2-alkenylphenols with ynamides has been developed toward the synthesis of spiro­[4,5]­decane derivatives.
Peng-Peng Lin (7355051)   +11 more
core   +2 more sources

Asymmetric Construction of Spiro[thio­pyrano­indole-benzo­isothiazole] Scaffold via a Formal [3 + 3] Spiroannulation

open access: yes, 2015
An enantioselective formal thio­[3 + 3] spiroannulation reaction of indoline-2-thiones to 1-azadienes has been developed by the use of a quinine-derived bifunctional tertiary amine-thiourea catalyst, which furnished a series of optically active spiro ...
Xing-Wang Wang (1538014)   +5 more
core   +1 more source

Ru(II)-Catalyzed Oxidative Spiroannulation of 2‑Arylphenols with Alkynes via a C–H Activation/Dearomatization Strategy

open access: yes, 2016
An intermolecular spiroannulation reaction of appropriately substituted 2-arylphenols with internal alkynes has been developed by using a Ru­(II) catalyst and an oxidant.
Yaoyu Wang (178722)   +6 more
core   +1 more source

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