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Acta Crystallographica. Section C : Structural Chemistry, ISSN 0108-2701, 12/2015, Volume 71, Issue 12, p. 1042
  Multicomponent crystals or cocrystals play a significant role in crystal engineering, the main objective of which is to understand the role of intermolecular... 
Molecular chemistry | Hydrogen bonds | Crystallography | Crystal structure
Journal Article
Acta Crystallographica Section C, ISSN 2053-2296, 12/2015, Volume 71, Issue 12, pp. 1042 - 1047
Journal Article
Acta Crystallographica Section C, ISSN 2053-2296, 12/2017, Volume 73, Issue 12, pp. 1056 - 1063
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 10/2017, Volume 2017, Issue 38, pp. 5763 - 5768
A new alkyne annulation strategy has been developed for the synthesis of polycyclic indole derivatives through a cascade of C–H annulation and Michael addition... 
Michael addition | Transition‐metal catalysis | Synthetic methods | Nitrogen heterocycles | Annulation | Polycycles | Transition-metal catalysis | CATALYZED ANNULATION | CHEMISTRY, ORGANIC | CASCADE | ALKYNES | C-H ACTIVATION | FUNCTIONALIZATION | N BOND FORMATION | DERIVATIVES | ACCESS | HYDROARYLATION | ALKALOIDS
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 12/2018, Volume 83, Issue 24, pp. 15361 - 15371
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 06/2018, Volume 2018, Issue 23, pp. 2963 - 2971
A mild domino rearrangement strategy for the direct access to substituted quinoline‐4‐carboxamides has been developed. This copper‐catalyzed coupling reaction... 
Oximes | Domino reactions | Nitrogen heterocycles | Copper | Ring expansion | SYMMETRICAL PYRIDINES | ISOQUINOLINES | KETOXIME CARBOXYLATES | EFFICIENT SYNTHESIS | CHEMISTRY, ORGANIC | ANTI-HIV-1 AGENTS | AMINATION | HETEROCYCLES | ACETATES | CASCADE ANNULATION | CYCLIZATION | Quinoline | Alkaloids | Bonds
Journal Article
Angewandte Chemie International Edition, ISSN 1433-7851, 02/2013, Volume 52, Issue 8, pp. 2251 - 2255
Skeletal diversity: The reactions of alkynoic acids (A, common type of substrates) with various scaffold‐building agents (B) under gold catalysis produce a... 
gold | alkynoic acids | branching cascade | molecular diversity | privileged scaffolds | STRATEGY | ALKYNES | CHEMISTRY, MULTIDISCIPLINARY | DOUBLE HYDROAMINATION | SKELETAL DIVERSITY | BIOLOGY | CHEMICAL SPACE | INHIBITORS | CYCLOISOMERIZATIONS | DERIVATIVES | Alkynes - chemistry | Molecular Structure | Catalysis | Carboxylic Acids - chemistry | Gold | Relay | Molecular structure | Catalysts | Cascades | Libraries | Scaffolds
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 04/2018, Volume 2018, Issue 14, pp. 1693 - 1698
A strategy has been developed for the synthesis of dispiro‐3H‐indoles by employing a 3‐({[2‐(1H‐indol‐3‐yl)ethyl]amino}methyl)but‐3‐en‐1‐ol derivative and... 
Sprio compounds | Heterocycles | Domino reactions | Cyclization | Diastereoselectivity | SYSTEM | SPIROCYCLIC INDOLENINES | OXONIUM-PRINS CYCLIZATION | STRATEGY | CHEMISTRY, ORGANIC | DISCOVERY | SCAFFOLDS | DERIVATIVES | Aldehydes
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 03/2015, Volume 2015, Issue 9, pp. 2038 - 2041
The three‐component coupling (3CC) of α‐diazoamide, aldehyde and 3‐arylideneoxindole using 5 mol‐% of Rh2(OAc)4 is described to afford a novel class of... 
Carbonyl ylides | Diazo compounds | Dispiro­oxindoles | Multicomponent reactions | 3‐Aryl­ideneoxindoles | 3-Aryl-ideneoxindoles | Dispiro-oxindoles | 3-Arylideneoxindoles | Dispirooxindoles | ONE-POT SYNTHESIS | DIOXOLANES | OXINDOLES | CHEMISTRY, ORGANIC | ALDEHYDES | DISCOVERY | 1,3-DIPOLAR CYCLOADDITION | REGIOSELECTIVE SYNTHESIS | CHEMISTRY | FACILE | DERIVATIVES | Aldehydes | Acetates
Journal Article
ORGANIC LETTERS, ISSN 1523-7060, 08/2019, Volume 21, Issue 16, pp. 6300 - 6304
A cationic Pd(IV)-catalyzed arylative hydroxylation-Micheal addition of allenyl-tethered cyclohexadienones was developed. This relay reaction could afford... 
CHEMISTRY, ORGANIC | ALDEHYDES | ARYLBORONIC ACIDS | DESYMMETRIZATION
Journal Article
The Journal of Organic Chemistry, ISSN 0022-3263, 11/2015, Volume 80, Issue 21, pp. 11162 - 11168
An efficient and mild one-pot, gold-catalyzed intramolecular cyclization of N-propargylic β-enaminones has been achieved for the generation of 1,4-oxazepine... 
CYCLOADDITION | HETEROCYCLES | ASYMMETRIC INDUCTION | AMOXAPINE | CHEMISTRY, ORGANIC | CYCLOISOMERIZATION | ANTI-DEPRESSANT | PYRROLES | HYDROAMINATION | HISTONE DEACETYLASE INHIBITORS | ALKALOIDS | Gold | Usage | Chemical properties | Catalysis | Chemical synthesis
Journal Article
Journal of the Academy of Marketing Science, ISSN 0092-0703, 9/2003, Volume 31, Issue 4, pp. 425 - 447
Journal Article
European Journal of Organic Chemistry, ISSN 1434-193X, 06/2019, Volume 2019, Issue 22, pp. 3567 - 3574
A wide array of aldehydes undergo smooth cross‐coupling with 5,6‐bis(2‐hydroxyethyl)‐2‐phenyl‐3a,4,7,7a‐tetrahydro‐1H‐isoindole‐1,3(2H)‐dione in the presence... 
Lewis acids | Isochromene scaffolds | Aldehydes | Prins bicyclization | Enediols | ALCOHOLS | ACTIVATION | RING | CHEMISTRY, ORGANIC | ALPHA | CYCLIZATION | Oxalic acid
Journal Article