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Chemical Communications, ISSN 1359-7345, 2010, Volume 46, Issue 14, pp. 2447 - 2449
A new organocatalytic quadruple domino Friedel-Crafts-type/Michael/Michael/aldol condensation reaction has been developed. In this one-pot multi-component... 
4 STEREOCENTERS | CASCADE REACTIONS | ENANTIOSELECTIVE SYNTHESIS | TRICYCLIC CARBON FRAMEWORKS | ONE-POT SYNTHESIS | NATURAL-PRODUCTS | ALKYLATION | ALPHA,BETA-UNSATURATED ALDEHYDES | DIPHENYLPROLINOL SILYL ETHER | CHEMISTRY, MULTIDISCIPLINARY | MICHAEL ADDITION
Journal Article
Chemical communications (Cambridge, England), ISSN 1359-7345, 08/2017, Volume 53, Issue 63, pp. 8882 - 8885
A heterogeneous enantioselective oxa-Michael-Michael reaction for the synthesis of chromans has been developed on a heterogeneous acid-base synergic catalyst... 
Journal Article
Chemistry - A European Journal, ISSN 0947-6539, 10/2009, Volume 15, Issue 42, pp. 11058 - 11076
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 05/2014, Volume 2014, Issue 13, pp. 2677 - 2681
Given the importance of indane derivatives in both organic and medicinal chemistry, the development of an effective synthetic protocol for the preparation of... 
Michael addition | Domino reactions | Nitrogen heterocycles | Enantioselectivity | Organocatalysis | ASYMMETRIC CATALYSIS | RECEPTOR ANTAGONISTS | 1,2,3-TRISUBSTITUTED INDANES | CHEMISTRY, ORGANIC | CASCADE | ORGANOCATALYSTS | INHIBITORS | INDANONES | CONGENERS | DERIVATIVES | Enantiomers | Thiophene
Journal Article
Organic Letters, ISSN 1523-7060, 04/2009, Volume 11, Issue 7, pp. 1627 - 1630
An unprecedented highly enantioselective cascade oxa-Michael-Michael reaction has been developed. The simple and practical process, efficiently catalyzed by... 
THIOCHROMANES | 4 STEREOCENTERS | ENANTIOENRICHED PIPERIDINES | DOMINO REACTIONS | ENANTIOSELECTIVE SYNTHESIS | ALKYLATION | CHEMISTRY, ORGANIC | CARBONYL-COMPOUNDS | ALDEHYDES | DIPHENYLPROLINOL SILYL ETHER | ION CATALYSIS
Journal Article
Organic Letters, ISSN 1523-7060, 05/2014, Volume 16, Issue 9, pp. 2438 - 2441
Application of indolin-3-one derivatives in a cascade reaction for efficient assembly of complex molecules is a much less explored research area. It is... 
CYCLOADDITION | ENANTIOSELECTIVE SYNTHESIS | STRATEGY | OXINDOLES | CHEMISTRY, ORGANIC | INDOLE ALKALOIDS | QUATERNARY | C-H INSERTION | Piperidines - chemistry | Magnetic Resonance Spectroscopy | Stereoisomerism | Indoles - chemical synthesis | Molecular Structure | Catalysis | Piperidines - chemical synthesis | Indoles - chemistry
Journal Article
Tetrahedron, ISSN 0040-4020, 01/2014, Volume 70, Issue 2, pp. 181 - 185
From -amino acid, three chiral thiophosphonodiamides were prepared as new hydrogen bond donor organocatalysts. Under the mediation of the catalyst derived from... 
2-(E)-2-Nitrovinylphenol | Malononitrile | 2-Amino-4H-chromene-3-carbonitrile | Tandem reaction | Thiophosphonodiamide | CHEMISTRY, ORGANIC | Hydrogen | Nitriles | Catalysts | Hydrogen bonds | Tetrahedrons | Catalysis | Mediation | Michael reaction
Journal Article
Chemical Communications, ISSN 1359-7345, 2017, Volume 53, Issue 63, pp. 8882 - 8885
A heterogeneous enantioselective oxa-Michael-Michael reaction for the synthesis of chromans has been developed on a heterogeneous acid-base synergic catalyst... 
CORE | S33084 | ASYMMETRIC-SYNTHESIS | REDUCTASE INHIBITOR | ANTAGONIST | MECHANISM | AMINES | CHROMENES | CHEMISTRY, MULTIDISCIPLINARY | ORGANIC FUNCTIONAL-GROUPS
Journal Article
Journal of the American Chemical Society, ISSN 0002-7863, 02/2007, Volume 129, Issue 5, pp. 1036 - 1037
Highly enantio- and diastereoselective tandem Michael-aldol reactions, efficiently catalyzed by a cinchona alkaloid thiourea via synergistic noncovalent... 
THIOLS | ASYMMETRIC-SYNTHESIS | DOMINO REACTIONS | STEREOCENTERS | MALONATE | NITROOLEFINS | DONORS | DERIVATIVES | CHEMISTRY, MULTIDISCIPLINARY | BIFUNCTIONAL ORGANOCATALYSTS | CONJUGATE ADDITION | Chemical reactions | Chemical properties | Hydrogen bonding | Analysis
Journal Article
Tetrahedron Letters, ISSN 0040-4039, 03/2019, Volume 60, Issue 12, pp. 839 - 842
A concise and straightforward formal synthesis of (±)-aplykurodinone-1, a degraded steroid natural product isolated from sea hare is described, based on an... 
Michael addition | Aplykurodinone-1 | Formal synthesis | Riley oxidation | DEGRADED STEROL | KETONE | CHEMISTRY, ORGANIC | Drugstores | Pharmacy | Biomedical engineering
Journal Article