Results 31 to 40 of about 337 (160)
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
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
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
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
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
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
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
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
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
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

