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Angewandte Chemie International Edition, ISSN 1433-7851, 12/2015, Volume 54, Issue 49, pp. 14929 - 14932
Journal Article
Chemical Communications, ISSN 1359-7345, 2017, Volume 53, Issue 54, pp. 7665 - 7668
Journal Article
Advanced Materials, ISSN 0935-9648, 12/2012, Volume 24, Issue 48, pp. 6484 - 6489
Journal Article
Chemical communications (Cambridge, England), ISSN 1359-7345, 07/2017, Volume 53, Issue 54, pp. 7665 - 7668
We report an efficient enantioselective conjugate addition of photogenerated α-amino radicals to Michael acceptors catalyzed by a newly prepared... 
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 05/2017, Volume 359, Issue 9, pp. 1541 - 1551
A cascade asymmetric Michael–intramolecular aldol‐lactonization of enals with oxindolyl β,γ‐unsaturated α‐keto esters was developed. An optically pure... 
oxindolyl β,γ-unsaturated α-keto esters | lactonization | spiro[cyclopentane-oxindoles] | intramolecular aldol reaction | N-heterocyclic carbine (NHC) catalysis
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 04/2014, Volume 2014, Issue 12, pp. 2460 - 2467
A practical and economical process for the synthesis of perfluoroalkylated indole compounds has been developed. The Michael addition of 2‐iodo‐ or... 
Michael addition | Synthetic methods | Nitrogen heterocycles | Copper | Annulation
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 09/2016, Volume 81, Issue 18, pp. 8296 - 8305
α,β-Unsaturated ynones have historically been used as Michael acceptors in conjugate addition reactions. Herein, we have demonstrated for the first time that... 
ACETYLACETONE | ALDOL ADDITIONS | ORGANOCATALYSTS | ASYMMETRIC CONJUGATE ADDITION | CATALYZED SYNTHESIS | AMINO-ACIDS | MALONATE | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | CYCLOISOMERIZATION | ENANTIOSELECTIVE ADDITION | Usage | Chemical properties | Catalysts | Carbon dioxide
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 2017, Volume 15, Issue 44, pp. 9465 - 9474
The asymmetric phospha-Michael addition of dialkyl phosphite to alpha,beta-unsaturated carbonyl compounds by using an azetidine-derived dinuclear zinc catalyst... 
HYDROPHOSPHINATION | N-ACYLPYRROLES | ENANTIOSELECTIVE 1,4-ADDITION | DIETHYL PHOSPHITE | PHOSPHONATES | CHEMISTRY, ORGANIC | ALDEHYDES | OXIDES | DIPHENYL PHOSPHITE | NITROALKENES | CONJUGATE ADDITION | Carbonyl compounds | Additives | Catalysis | Catalysts | Zinc | Carbonyls
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 03/2011, Volume 76, Issue 5, pp. 1472 - 1474
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 08/2013, Volume 2013, Issue 22, pp. 4738 - 4743
Pyrazoles are an important class of molecular structures with significant biological and pharmaceutical activities. Herein, heterocyclic compounds containing... 
Azlactones | Amino acids | Asymmetric synthesis | Nitrogen heterocycles | Organocatalysis | HIGHLY REGIO | CHEMISTRY, ORGANIC | ALPHA-AMINO-ACIDS | UNSATURATED PYRAZOLONES | DIASTEREO | MICHAEL ADDITION | SPIROPYRAZOLONES | HETEROCYCLES | MALEIMIDES | OXAZOLONES | DERIVATIVES
Journal Article
Organic & biomolecular chemistry, ISSN 1477-0520, 11/2017, Volume 15, Issue 44, pp. 9465 - 9474
The asymmetric phospha-Michael addition of dialkyl phosphite to α,β-unsaturated carbonyl compounds by using an azetidine-derived dinuclear zinc catalyst was... 
Journal Article
Organic Letters, ISSN 1523-7060, 07/2015, Volume 17, Issue 13, pp. 3283 - 3285
2-Perfluoroalkylated indoles were efficiently synthesized via a one-pot cascade Michael-type addition/palladium-catalyzed intramolecular cross-dehydrogenative... 
FUNCTIONALIZATION | FACILE SYNTHESIS | ANNULATION | ANILINES | CHEMISTRY, ORGANIC | INDOLE SYNTHESIS | BOND | REGIOSELECTIVITY | C-H ACTIVATION | DERIVATIVES | CYCLIZATION
Journal Article
Tetrahedron, ISSN 0040-4020, 07/2015, Volume 71, Issue 28, pp. 4629 - 4634
A Michael-Michael-acetalization cascade between 4-(2-hydroxyphenyl)but-3-en-2-ones and α,β-unsaturated aldehydes via a novel dual activation mode promoted by... 
Cascade reaction | Chromen | Polycycle | Dually activation mode | CHROMANS | CATALYSIS | DOMINO REACTIONS | CHEMISTRY, ORGANIC | INTERMEDIATE | DERIVATIVES | CYCLIZATION | Hydroxides
Journal Article
Organic and Biomolecular Chemistry, ISSN 1477-0520, 11/2013, Volume 11, Issue 42, pp. 7393 - 7399
A new reaction model, tandem Michael addition/formal isocyanide insertion into the acyl C-C bond, has been developed. Thus, a series of 2-acylpyrroles and... 
TOSYLMETHYL ISOCYANIDE | CATALYZED 3-COMPONENT REACTION | COMPLEX CATALYST | OLIGOSUBSTITUTED PYRROLES | SYNTHETIC REACTIONS | SULFONYLMETHYL ISOCYANIDES | REGIOSELECTIVE SYNTHESIS | CHEMISTRY, ORGANIC | TERMINAL ALKYNES | ISOCYANIDE INSERTION | H ACTIVATION
Journal Article