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Chemistry, an Asian journal, ISSN 1861-4728, 10/2016, Volume 11, Issue 20, pp. 2829 - 2833
.... In addition, a proposed mechanism has been confirmed for this reaction. It′s very convenient: A convenient one‐pot route for the synthesis of 3... 
Michael addition | aldol reaction | aldehydes | cycloaddition | 4-quinolones | Physical Sciences | Chemistry | Chemistry, Multidisciplinary | Science & Technology | Aldehydes
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 04/2018, Volume 24, Issue 19, pp. 4909 - 4915
...‐mediated asymmetric direct aldol reaction of two different aldehydes, followed by either Wittig or Horner–Wadsworth–Emmons reactions... 
organocatalysis | asymmetric synthesis | diols | domino reactions | synthesis design | Glycols | Synthesis | Catalysis | Aldehydes | Organic compounds | Ketones | Reagents | Cascade chemical reactions | Enantiomers | Chemical synthesis | Diols | Michael reaction
Journal Article
Advanced synthesis & catalysis, ISSN 1615-4150, 08/2017, Volume 359, Issue 16, pp. 2824 - 2831
...‐threonine and l‐serine potassium salt‐catalyzed reactions proceed even when the nucleophilic and electrophilic Michael partners simultaneously contain acidic spectator groups... 
carboxylate salt bridge | organocatalysis | nitroalkenes | maleimide | Michael reaction | peracetic acid | Catalysis | Enantiomers | Antidepressants | Organic acids | Catalysts | Phenols | Chemical reactions | Tolerances | Carboxylic acids | Potassium
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 02/2018, Volume 57, Issue 9, pp. 2464 - 2468
.... We now describe an efficient, general, and highly enantioselective Mukaiyama–Michael reaction of silyl ketene acetals with α,β... 
organocatalysis | cinnamates | Mukaiyama–Michael reaction | silyl ketene acetals | Brønsted acids | Lewis acid | Esters | Catalysis | Enantiomers | Acetals | Substrates | Michael reaction
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 10/2016, Volume 22, Issue 44, pp. 15650 - 15653
A highly regio‐, diastereo‐ and enantioselective Michael addition–alkylation reaction between α... 
organocatalysis | chiral N,N′-dioxide | asymmetric catalysis | 2,3-dihydrofuran | Michael alkylation
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 07/2018, Volume 57, Issue 29, pp. 9088 - 9092
By employing a simple in situ generated magnesium catalyst, a direct asymmetric reaction between hemiacetals and phosphorus ylides was achieved through a tandem Wittig–oxa... 
phosphorus ylides | magnesium | asymmetric synthesis | hemiacetals | chiral ethers | Enantiomers | Synthesis | Organic compounds | Organic chemistry | Nucleotide sequence | Triphenylphosphine oxide | Byproducts | Phosphorus | Magnesium | Chemical synthesis | Michael reaction
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 07/2018, Volume 57, Issue 30, pp. 9397 - 9401
...Intramolecular aza‐Michael reactions are one of the most efficient and powerful tools for accessing N heterocycles in a straightforward manner. Continuous... 
Michael addition | organocatalysis | asymmetric synthesis | heterocycles | synthetic methods | Amides | Synthesis | Catalysis | Enantiomers | Organic compounds | Thioesters | Catalysts | Core loss | Esters | Oxidation | Chemical synthesis | Substrates | Michael reaction | Tetrahydropyridines
Journal Article
Chemistry : a European journal, ISSN 0947-6539, 10/2016, Volume 22, Issue 42, pp. 15119 - 15124
A highly enantioselective tandem Michael/ring‐closure reaction of α,β‐unsaturated pyrazoleamides and amidomalonates has been accomplished in the presence of a chiral N,N′‐dioxide–Yb(OTf)3 complex (Tf... 
asymmetric synthesis | paroxetine | ring-closure reactions | Michael reactions | heterocycles | Index Medicus
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 12/2015, Volume 54, Issue 51, pp. 15414 - 15418
The aza‐Michael addition reaction is a vital transformation for the synthesis of functionalized chiral amines... 
noncovalent catalysis | aliphatic amines | aza‐Michael addition | asymmetric catalysis | N‐heterocyclic carbenes | aza-Michael addition | N-heterocyclic carbenes
Journal Article
Angewandte Chemie (International ed.), ISSN 1433-7851, 09/2016, Volume 55, Issue 39, pp. 12104 - 12108
An asymmetric organocatalytic domino oxa‐Michael/1,6‐addition reaction of ortho‐hydroxyphenyl‐substituted para‐quinone methides and isatin... 
organocatalysis | para-quinone methides | oxa-Michael addition | domino reactions | chromans | Synthesis | Oxalic acid | Quinone | Organic compounds
Journal Article