Access the full text.
Sign up today, get DeepDyve free for 14 days.
(1989)
Montaufier, S.L. Randriamahefa
Sanny Verma, Harshal Mungse, Neeraj Kumar, Shivani Choudhary, S. Jain, B. Sain, O. Khatri (2011)
Graphene oxide: an efficient and reusable carbocatalyst for aza-Michael addition of amines to activated alkenes.Chemical communications, 47 47
Leandro Monsalve, Florencia Gillanders, A. Baldessari (2012)
Promiscuous Behavior of Rhizomucor miehei Lipase in the Synthesis of N‐Substituted β‐Amino EstersEuropean Journal of Organic Chemistry, 2012
B. Das, Nikhil Chowdhury (2007)
Amberlyst-15: An efficient reusable heterogeneous catalyst for aza-Michael reactions under solvent-free conditionsJournal of Molecular Catalysis A-chemical, 263
Yogesh Sharma, M. Degani (2007)
Green and mild protocol for hetero-Michael addition of sulfur and nitrogen nucleophiles in ionic liquidJournal of Molecular Catalysis A-chemical, 277
M. Chaudhuri, Sahid Hussain, M. Kantam, B. Neelima (2005)
Boric acid: a novel and safe catalyst for aza-Michael reactions in waterTetrahedron Letters, 46
Wing‐Leung Wong, Kwok‐yin Wong (2012)
Recent development in functionalized ionic liquids as reaction media and promotersCanadian Journal of Chemistry, 90
V. Polshettiwar, R. Varma (2010)
Nano-organocatalyst: magnetically retrievable ferrite-anchored glutathione for microwave-assisted Paal–Knorr reaction, aza-Michael addition, and pyrazole synthesisTetrahedron, 66
G. Bartoli, M. Bosco, E. Marcantoni, M. Petrini, L. Sambri, E. Torregiani (2001)
Conjugate Addition of Amines to α,β-Enones Promoted by CeCl3·7H2O−NaI System Supported in Silica GelJournal of Organic Chemistry, 66
M. Kantam, S. Laha, J. Yadav, S. Jha (2009)
Nanocrystalline copper(II) oxide catalyzed aza-Michael reaction and insertion of α-diazo compounds into N–H bonds of aminesTetrahedron Letters, 50
Li‐Wen Xu, C. Xia (2004)
Highly efficient phosphine-catalyzed aza-Michael reactions of α,β-unsaturated compounds with carbamates in the presence of TMSClTetrahedron Letters, 45
X. Liu, M. Lu, G. Gu, T. Lu (2011)
Aza-Michael reactions in water using functionalized ionic liquids as the recyclable catalystsJournal of the Iranian Chemical Society, 8
J. Cabral, P. Laszlo, L. Mahe, M. Montaufier, S. Randriamahefa (1989)
Catalysis of the specific michael addition : The example of acrylate acceptorsTetrahedron Letters, 30
L. Nguyen, T. Nguyen, K. Nguyen, N. Phan (2012)
Metal–organic framework MOF-199 as an efficient heterogeneous catalyst for the aza-Michael reactionApplied Catalysis A-general, 425
P. Wasserscheid, W. Keim (2000)
Ionic Liquids-New "Solutions" for Transition Metal Catalysis.Angewandte Chemie, 39 21
M. Kantam, Moumita Roy, Sarabindu Roy, B. Sreedhar, R. De (2008)
Polyaniline supported CuI: An efficient catalyst for C–N bond formation by N-arylation of N(H)-heterocycles and benzyl amines with aryl halides and arylboronic acids, and aza-Michael reactions of amines with activated alkenesCatalysis Communications, 9
K. Surendra, N. Krishnaveni, R. Sridhar, K. Rao (2006)
β-Cyclodextrin promoted aza-Michael addition of amines to conjugated alkenes in waterTetrahedron Letters, 47
J. Yadav, B. Reddy, A. Basak, A. Narsaiah (2003)
Aza-Michael Reactions in Ionic Liquids. A Facile Synthesis of β-Amino CompoundsChemistry Letters, 32
Li-yan Dai, Yi Zhang, Qianqian Dou, Xiao-zhong Wang, Ying-qi Chen (2013)
Chemo/regioselective Aza-Michael additions of amines to conjugate alkenes catalyzed by polystyrene-supported AlCl3Tetrahedron, 69
(2011)
Comparison of this catalyst with other reported catalysts in the model reaction between morphine and acrylonitrile Entry Reaction conditions Yield
Yan Wang, Yan‐qin Yuan, Sheng-rong Guo (2009)
Silica Sulfuric Acid Promotes Aza-Michael Addition Reactions under Solvent-Free Condition as a Heterogeneous and Reusable CatalystMolecules, 14
G. Bartoli, C. Cimarelli, E. Marcantoni, G. Palmieri, M. Petrini (1994)
Chemo- and Diastereoselective Reduction of .beta.-Enamino Esters: A Convenient Synthesis of Both cis- and trans-.gamma.-Amino Alcohols and .beta.-Amino EstersJournal of Organic Chemistry, 59
(1267)
Chem
The recyclable ionic liquid [ADPQ][CH3COO] has been used as catalyst for aza-Michael addition of amines to α, β-unsaturated compounds to produce β-amino compounds. The reactions were complete in a few hours with high yields. The ionic liquid can be recycled and reused six times without noticeable decrease of catalytic activity.
Research on Chemical Intermediates – Springer Journals
Published: Feb 15, 2015
Access the full text.
Sign up today, get DeepDyve free for 14 days.