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Angewandte Chemie International Edition, ISSN 1433-7851, 08/2015, Volume 54, Issue 33, pp. 9523 - 9527
Journal Article
Journal of Chemical Research, ISSN 1747-5198, 03/2017, Volume 41, Issue 3, pp. 168 - 171
Seventeen examples of 2,6-diarylspiro[cyclohexane-1,3'-indoline]-2', 4-diones were efficiently prepared by the Cs2CO3-catalysed chemoselective double Michael... 
Double Michael addition | Divinyl ketone | Spiro[cyclohexane-1,3'-indoline]-2',4-dione | Indolin-2-one | OXINDOLES | divinyl ketone | spiro[cyclohexane-1,3 '-indoline]-2 '-4-dione | double Michael addition | CHEMISTRY, MULTIDISCIPLINARY | indolin-2-one | Ketones | Diketones | Cyclohexane
Journal Article
Journal of Organic Chemistry, ISSN 0022-3263, 06/2015, Volume 80, Issue 11, pp. 5704 - 5712
A highly efficient N,N'-diokide/Gd(III) complex has been developed for the enantioselective conjugate addition of nitroalkanes to alpha,beta-unsaturated... 
ORGANOCATALYSTS | LIGANDS | AMINO-ACIDS | CHEMISTRY, ORGANIC | ENANTIOSELECTIVE MICHAEL ADDITION | EFFICIENT | NITROMETHANE | Nitro compounds | Gadolinium | Chemical properties | Catalysis | Research | Heterocyclic aromatic compounds
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 03/2017, Volume 56, Issue 14, pp. 4006 - 4010
The enantioselective α‐addition of deconjugated butenolides has rarely been exploited, in contrast to the well‐studied γ‐addition of deconjugated butenolides.... 
butenolides | ortho | dihydrocoumarins | asymmetric catalysis | quinone methides | nucleophilic addition | ortho-quinone methides | ORGANIC-SYNTHESIS | ASYMMETRIC-SYNTHESIS | VINYLOGOUS MICHAEL REACTIONS | NATURAL-PRODUCTS | O-QUINONE METHIDES | CHEMISTRY, MULTIDISCIPLINARY | GAMMA-SUBSTITUTED BUTENOLIDES | ALKYLATING-AGENTS | DIELS-ALDER REACTION | G-QUADRUPLEX | CONJUGATE ADDITION
Journal Article
Tetrahedron, ISSN 0040-4020, 09/2014, Volume 70, Issue 37, pp. 6522 - 6528
A practical, convenient, and safe cyano(nitro)methylation method was developed, in which cyano- -nitroacetate served as a synthetic equivalent of anionic... 
Michael addition | Polyfunctionalized compound | Pyridine | [1,8]-Naphthyridine | Nitroacetonitrile | Naphthyridine | CHEMISTRY, ORGANIC | CATALYST | DERIVATIVES | EFFICIENT | Pyridines | Synthesis | Equivalence | Precursors | Tetrahedrons | Michael reaction | Adducts
Journal Article
Tetrahedron: Asymmetry, ISSN 0957-4166, 2007, Volume 18, Issue 3, pp. 299 - 365
Journal Article
Chemistry – A European Journal, ISSN 0947-6539, 05/2017, Volume 23, Issue 27, pp. 6509 - 6513
An unprecedented Rauhut–Currier‐type 1,6‐conjugate addition has been developed. With chiral cyclohexane‐based phosphine‐amide catalyst 3 h , the 1,6‐conjugate... 
quinone methide | chiral phosphine | asymmetric catalysis | conjugation | rauhut-currier | MORITA-BAYLIS-HILLMAN | CYSTEINE | THIOUREA-PHOSPHINE | MULTIFUNCTIONAL CHIRAL PHOSPHINE | CHEMISTRY, MULTIDISCIPLINARY | ACTIVATED ALKENES | ORGANOCATALYSTS | MICHAEL CYCLOISOMERIZATION | ESTERS | ALPHA-AMINO-ACID | Catalysis | Enantiomers | Quinone | Cyclohexane | Catalysts | Quinones | Amides
Journal Article