62680-47-1Relevant academic research and scientific papers
Enantioselective N-Heterocyclic Carbene Catalysis that Exploits Imine Umpolung
Fernando, Jared E. M.,Nakano, Yuji,Zhang, Changhe,Lupton, David W.
supporting information, p. 4007 - 4011 (2019/02/24)
The catalytic umpolung of imines remains an underdeveloped approach to reaction discovery. Herein we report an enantioselective aza-Stetter reaction that proceeds via imine umpolung using N-heterocyclic carbene catalysis. The reaction proceeds with high l
Structure-reactivity relationships of alkyl α-hydroxymethacrylate derivatives
Karahan, Ozlem,Avci, Duygu,Avaeyente, Vaektorya
experimental part, p. 3058 - 3068 (2012/05/05)
A series of alkyl α-hydroxymethacrylate derivatives with various secondary functionalities (ether, ester, carbonate, and carbamate) and terminal groups (alkyl, cyano, oxetane, cyclic carbonate, phenyl and morpholine) were synthesized to investigate the ef
Isoxazoline derivative and a process for the preparation thereof
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Page/Page column 39, (2010/02/07)
The present invention provides to an isoxazoline derivative of formula (I), the pharmaceutically acceptable salts, esters and stereochemically isomeric forms thereof, and the use of the derivative in inhibiting the activity of caspases. The present invent
Synergy or competition between palladium-catalysis and KF/alumina-mediation for the allylic substitution of the acetates of Baylis-Hillman adducts by phenols
Roy, Olivier,Riahi, Abdelkhalek,Hénin, Fran?oise,Muzart, Jacques
, p. 8133 - 8140 (2007/10/03)
The addition of various substituted phenols [XC6H4OH, X=H, o-CHO, o-CO2Me, o-CO2CH2Ph, o-CN, m-NHCOMe, m-OMe, p-OMe, p-CHO, p-Cl] to allylic acetates obtained from Baylis-Hillman adducts [RCH(OAc)C(=C
STUDIES IN CLAISEN REARRANGEMENT; NOVEL THERMAL TRANSFORMATION OF α-ARYLOXYMETHYLACRYLIC ACIDS AND THEIR DERIVATIVES
Gopalan, B.,Rajagopalan, K.,Sunitha, K.,Balasubramanian, K. K.
, p. 3153 - 3160 (2007/10/02)
α-Aryloxymethylacrylic acids and their derivatives have been found to undergo some novel thermal transformations leading to the formation of 'ene' dimers.The structure of the dimer has been revised on the basis of degradation studies, extensive spectral data and isolation of intermediates.
